| Q89873567 | 18q12.3-q21.1 microdeletion detected in the prenatally alcohol-exposed dizygotic twin with discordant fetal alcohol syndrome phenotype |
| Q40022869 | A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development |
| Q35928262 | A Common Phenotype Polymorphism in Mammalian Brains Defined by Concomitant Production of Prolactin and Growth Hormone |
| Q33877341 | A Generalized Linear Model for Decomposing Cis-regulatory, Parent-of-Origin, and Maternal Effects on Allele-Specific Gene Expression |
| Q31097583 | A Prevalence of Imprinted Genes within the Total Transcriptomes of Human Tissues and Cells |
| Q67482957 | A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression |
| Q36710170 | A complex deoxyribonucleic acid looping configuration associated with the silencing of the maternal Igf2 allele |
| Q32085871 | A conserved structural element in horse and mouse IGF2 genes binds a methylation sensitive factor |
| Q22008676 | A family of insulin-like growth factor II mRNA-binding proteins represses translation in late development |
| Q36084319 | A monoallelic-to-biallelic T-cell transcriptional switch regulates GATA3 abundance |
| Q35017116 | A new imprinted gene cloned by a methylation-sensitive genome scanning method |
| Q36949891 | A novel H19 antisense RNA overexpressed in breast cancer contributes to paternal IGF2 expression |
| Q40810626 | A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms. |
| Q33862945 | A novel variant of Inpp5f is imprinted in brain, and its expression is correlated with differential methylation of an internal CpG island |
| Q49057890 | A paternal-specific methylation imprint marks the alleles of the mouse H19 gene |
| Q62745950 | A paternally expressed QTL affecting skeletal and cardiac muscle mass in pigs maps to the IGF2 locus |
| Q37302230 | A randomly integrated transgenic H19 imprinting control region acquires methylation imprinting independently of its establishment in germ cells |
| Q46050836 | A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis |
| Q35221526 | A survey for novel imprinted genes in the mouse placenta by mRNA-seq |
| Q38028387 | A survey of tissue-specific genomic imprinting in mammals |
| Q35199693 | A transcriptional insulator at the imprinted H19/Igf2 locus |
| Q42020735 | A versatile genetic tool: haploid cells. |
| Q73747003 | ARHI is the center of allelic deletion on chromosome 1p31 in ovarian and breast cancers |
| Q42711452 | Aberrant DNA methylation at Igf2-H19 imprinting control region in spermatozoa upon neonatal exposure to bisphenol A and its association with post implantation loss |
| Q33318984 | Aberrant epigenetic changes and gene expression in cloned cattle dying around birth |
| Q46640058 | Abnormal Igf2 gene in Prague hereditary hypertriglyceridemic rats: its relation to blood pressure and plasma lipids |
| Q46225236 | Abnormal development of embryonic and extraembryonic cell lineages in parthenogenetic mouse embryos |
| Q48016474 | Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest |
| Q50953860 | Actions and interactions of growth hormone and insulin-like growth factor-II: body and organ growth of transgenic mice. |
| Q36695478 | Activation of an imprinted Igf 2 gene in mouse somatic cell cultures |
| Q34236278 | Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma |
| Q51814326 | Additional evidence for the genomic imprinting model of sex determination in the haplodiploid wasp Nasonia vitripennis: isolation of biparental diploid males after X-ray mutagenesis. |
| Q73535597 | Adrenocortical carcinoma |
| Q57645859 | Adrenocortical carcinoma |
| Q37850996 | Adrenocortical carcinoma: a clinician's update |
| Q38659703 | Adrenocortical tumors and insulin resistance: What is the first step? |
| Q33910487 | Adult mice cloned from migrating primordial germ cells |
| Q28741608 | Advanced computational biology methods identify molecular switches for malignancy in an EGF mouse model of liver cancer |
| Q48084682 | Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting |
| Q50717356 | Allele-specific detection of nascent transcripts by fluorescence in situ hybridization reveals temporal and culture-induced changes in Igf2 imprinting during pre-implantation mouse development. |
| Q40394401 | Allele-specific gene expression in mammals: the curious case of the imprinted RNAs |
| Q35308720 | Allele-specific parental imprinting of dzr1, a posttranscriptional regulator of zein accumulation |
| Q41541045 | Allele-specific replication timing of imprinted gene regions |
| Q37781386 | Allelic exclusion of immunoglobulin genes: models and mechanisms |
| Q73666171 | Allelic expression of the putative tumor suppressor gene p73 in human fetal tissues and tumor specimens |
| Q34726828 | Allelic inactivation regulates olfactory receptor gene expression |
| Q59607836 | Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locusPGL |
| Q37082182 | Alterations in expression of imprinted genes from the H19/IGF2 loci in a multigenerational model of intrauterine growth restriction (IUGR). |
| Q37251251 | Alterations in methylation and expression levels of imprinted genes H19 and Igf2 in the fetuses of diabetic mice |
| Q46899063 | Alterations in the promoter-specific imprinting of the insulin-like growth factor-II gene in Wilms' tumor |
| Q35102519 | Altered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placenta |
| Q51954217 | Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae. |
| Q47604904 | An essential role for IGF2 in cartilage development and glucose metabolism during postnatal long bone growth. |
| Q37136956 | An extensive genetic program occurring during postnatal growth in multiple tissues |
| Q35716850 | An overview of developmental genetics in mammals |
| Q38293466 | Analysis of genomic imprinting of Gs alpha gene. |
| Q33976541 | Analysis of imprinted gene expression in normal fertilized and uniparental preimplantation porcine embryos |
| Q50683487 | Analysis of imprinted messenger RNA expression during bovine preimplantation development. |
| Q35856849 | Analysis of the H19ICR insulator |
| Q74403446 | Analysis of the methylation status of imprinted genes based on methylation-specific polymerase chain reaction combined with denaturing high-performance liquid chromatography |
| Q35927951 | Ancient and continuing Darwinian selection on insulin-like growth factor II in placental fishes |
| Q34793925 | Antagonistic roles in fetal development and adult physiology for the oppositely imprinted Grb10 and Dlk1 genes |
| Q31147226 | Antisense transcripts with FANTOM2 clone set and their implications for gene regulation |
| Q36643840 | Are cranial germ cell tumours really tumours of germ cells? |
| Q60305273 | Association of Copy Number Variation at Intron 3 of With Navel Length in |
| Q28305462 | Association of IGF2 and H19 imprinting with choriocarcinoma development |
| Q33817092 | Asymmetric paternal effect on offspring size linked to parent-of-origin expression of an insulin-like growth factor |
| Q55717962 | Atlas of tissue- and developmental stage specific gene expression for the bovine insulin-like growth factor (IGF) system. |
| Q38566647 | Autocrine and Paracrine Actions of IGF-I Signaling in Skeletal Development |
| Q34442748 | BACs as tools for the study of genomic imprinting |
| Q39452858 | BMP signaling induces visceral endoderm differentiation of XEN cells and parietal endoderm |
| Q35635745 | BMP4 signaling directs primitive endoderm-derived XEN cells to an extraembryonic visceral endoderm identity. |
| Q54560423 | Bacterial infection promotes DNA hypermethylation. |
| Q38089794 | Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth |
| Q72819474 | Beckwith-Wiedemann syndrome |
| Q42176265 | Beckwith-Wiedemann syndrome and the insulin-like growth factor-II gene. Does the genotype explain the phenotype? |
| Q35716500 | Beckwith-Wiedemann syndrome, tumourigenesis and imprinting |
| Q48443147 | Biallelic expression of all four IGF-II promoters and its association with increased methylation of H19 gene in human brain |
| Q46630830 | Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting |
| Q28269422 | Biallelic expression of the H19 and IGF2 genes in hepatocellular carcinoma |
| Q73106365 | Biallelic transcription of Igf2 and H19 in individual cells suggests a post-transcriptional contribution to genomic imprinting |
| Q36883554 | Bioactive factors for tissue regeneration: state of the art. |
| Q41789322 | Biochemical characterization of individual human glycosylated pro-insulin-like growth factor (IGF)-II and big-IGF-II isoforms associated with cancer. |
| Q57267877 | Bioinformatics for High-Throughput Toxico-Epigenomics Studies |
| Q36891056 | Biological aspects of cytosine methylation in eukaryotic cells |
| Q37963987 | Biology and significance of signalling pathways activated by IGF-II. |
| Q41558016 | Biosynthesis of 10 kDa and 7.5 kDa insulin-like growth factor II in a human rhabdomyosarcoma cell line |
| Q34620395 | Brain function and chromatin plasticity |
| Q50988370 | C-peptide, insulin-like growth factors I and II, and insulin-like growth factor binding protein-1 in cord serum of twins: genetic versus environmental regulation. |
| Q28075872 | CRISPR-Mediated Epigenome Editing |
| Q40935490 | Cancer. Exploring the bowels of DNA methylation |
| Q52532641 | Caprine testicular hypoplasia associated with sexual reversion decreases the expression of insulin-like growth factor II (IGF-II) mRNA in testes. |
| Q74461116 | Cardiomyopathy in mice with paternal uniparental disomy for chromosome 12 |
| Q33285306 | Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. |
| Q33191658 | Cell-specific expression of a Clara cell secretory protein-human growth hormone gene in the bronchiolar epithelium of transgenic mice |
| Q36492692 | Changing images of the gene |
| Q34292385 | Chest wall hamartoma with Wiedemann-Beckwith syndrome: clinical report and brief review of chromosome 11p15.5-related tumors |
| Q30466805 | Child health, developmental plasticity, and epigenetic programming |
| Q33749246 | Choline, Other Methyl-Donors and Epigenetics |
| Q48352508 | Chromatin conformation of the H19 epigenetic mark |
| Q41387004 | Chromatin structure and imprinting: developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene. |
| Q36238491 | Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters. |
| Q35077074 | Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation. |
| Q30664234 | Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesis |
| Q52189130 | Co-dominant expression of the HLA-G gene and various forms of alternatively spliced HLA-G mRNA in human first trimester trophoblast. |
| Q36844969 | Colorectal cancer epigenetics: the role of environmental factors and the search for molecular biomarkers |
| Q47749049 | Comparative analysis of the IGF2 and ZBED6 gene variants and haplotypes reveals significant effect of growth traits in cattle |
| Q40415818 | Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region. |
| Q33887777 | Competition--a common motif for the imprinting mechanism? |
| Q36436496 | Complementation hypothesis: the necessity of a monoallelic gene expression mechanism in mammalian development. |
| Q33691538 | Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality |
| Q24684684 | Computational and experimental identification of novel human imprinted genes |
| Q37635469 | Concise review: parthenote stem cells for regenerative medicine: genetic, epigenetic, and developmental features |
| Q24617076 | Condensin and cohesin complexity: the expanding repertoire of functions |
| Q36605372 | Conditional deletions refine the embryonic requirement for Dlk1. |
| Q24337027 | Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism |
| Q34097141 | Control of fetal growth and neonatal survival by the RasGAP-associated endoribonuclease G3BP. |
| Q50061707 | Correlation of Insulin-Like Growth Factor-I and -II Concentrations at Birth Measured by Mass Spectrometry and Growth from Birth to Two Months. |
| Q21563370 | Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective |
| Q57807472 | Current status and strategies of long noncoding RNA research for diabetic cardiomyopathy |
| Q50422488 | DNA Methylation Dynamics of Genomic Imprinting in Mouse Development. |
| Q31742998 | DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts |
| Q47597020 | DNA methylation and expression of imprinted genes are associated with the viability of different sexual cloned buffaloes. |
| Q41743008 | DNA methylation and genome imprinting in the zebrafish, Danio rerio: some evolutionary ramifications |
| Q29615417 | DNA methylation and human disease |
| Q41566233 | DNA methylation and imprinting: why bother? |
| Q41439642 | DNA methylation in genomic imprinting |
| Q34378421 | DNA methylation in genomic imprinting, development, and disease |
| Q38834298 | DNA methylation in hematopoietic development and disease |
| Q36551951 | DNA methylation: a phoenix rises |
| Q45239557 | Dads and disomy and disease |
| Q41333775 | De Novo Mutation of Paternal IGF2 Gene Causing Silver-Russell Syndrome in a Sporadic Patient |
| Q48056435 | De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome |
| Q37456221 | Deciphering Brain Insulin Receptor and Insulin-Like Growth Factor 1 Receptor Signalling. |
| Q34107722 | Defining the pathway to insulin-like growth factor system targeting in cancer |
| Q53625137 | Delayed and disturbed morphogenesis of the umbilical blood vessels in insulin-like growth factor-II deficient conceptuses (Igf2m+/p-). |
| Q35211749 | Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. |
| Q46146329 | Deregulation of both imprinted and expressed alleles of the insulin–like growth factor 2 gene during β–cell tumorigenesis |
| Q37460341 | Derivation of embryonic stem cell lines from parthenogenetically developing rat blastocysts |
| Q33305278 | Dermal fibroblasts derived from fetal and postnatal humans exhibit distinct responses to insulin like growth factors |
| Q38716738 | Detection of Imprinted Genes by Single-Cell Allele-Specific Gene Expression |
| Q35834227 | Developmental and tissue-specific expression of prosaposin mRNA in murine tissues |
| Q52216862 | Developmental changes in methylation of spermatogenesis-specific genes include reprogramming in the epididymis. |
| Q50529556 | Developmental changes of Insulin-like growth factors in the liver and muscle of chick embryos. |
| Q52214150 | Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes |
| Q34030154 | Developmental stage-specific interplay of GATA1 and IGF signaling in fetal megakaryopoiesis and leukemogenesis |
| Q50014666 | Dietary Modulation of the Epigenome |
| Q36244244 | Dietary factors, genetic and epigenetic influences in colorectal cancer |
| Q36119580 | Differences between homologous alleles of olfactory receptor genes require the Polycomb Group protein Eed. |
| Q34019927 | Different yet similar: evolution of imprinting in flowering plants and mammals |
| Q34186007 | Differential differences in methylation status of putative imprinted genes among cloned swine genomes |
| Q34086662 | Differential expression of insulin-like growth factors I and II (IGF I and II), mRNA, peptide and binding protein 1 during mouse palate development: comparison with TGF beta peptide distribution |
| Q42096182 | Differential genomic imprinting regulates paracrine and autocrine roles of IGF2 in mouse adult neurogenesis |
| Q64054006 | Differential roles of insulin like growth factor 1 receptor and insulin receptor during embryonic heart development |
| Q33966144 | Differentiation of single cell derived human mesenchymal stem cells into cells with a neuronal phenotype: RNA and microRNA expression profile. |
| Q48798047 | Differentiation potential of histocompatible parthenogenetic embryonic stem cells |
| Q40957469 | Diminished G1 checkpoint after gamma-irradiation and altered cell cycle regulation by insulin-like growth factor II overexpression |
| Q52106237 | Diploid-dependent regulation of gene expression: a genetic cause of abnormal development in fish haploid embryos. |
| Q73764736 | Disruption of imprinted expression of U2afbp-rs/U2af1-rs1 gene in mouse parthenogenetic fetuses |
| Q28287765 | Disruption of imprinting caused by deletion of the H19 gene region in mice |
| Q41523994 | Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome |
| Q24642008 | Disruption of the Fbxw8 gene results in pre- and postnatal growth retardation in mice |
| Q35167917 | Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism |
| Q28288697 | Dissociation of IGF2 and H19 imprinting in human brain |
| Q48569816 | Distribution of androgenetic cells in fetal mouse chimeras |
| Q31800343 | Does genomic imprinting contribute to valproic acid teratogenicity? |
| Q72345863 | Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution |
| Q52660210 | Drosophila Su(Hw) regulates an evolutionarily conserved silencer from the mouse H19 imprinting control region. |
| Q28140399 | Duplication of genes encoding non-clathrin coat protein gamma-COP in vertebrate, insect and plant evolution |
| Q52128191 | Dynamic temporal and spatial regulation of the cdk inhibitor p57(kip2) during embryo morphogenesis. |
| Q55104154 | Early prenatal alcohol exposure alters imprinted gene expression in placenta and embryo in a mouse model. |
| Q34039461 | Eating fish for two |
| Q39564313 | Effect of in ovo folic acid injection on hepatic IGF2 expression and embryo growth of broilers |
| Q28580888 | Effect of nicotine exposure during pregnancy and lactation on maternal, fetal, and postnatal rat IGF-II profile |
| Q100634072 | Effects of feeding frequency on juvenile Chinese sturgeon Acipenser sinensis |
| Q74560571 | Effects of fibroblast growth factor 2 and insulin-like growth factor II on the development of parthenogenetic mouse embryos in vitro |
| Q37238992 | Effects of genomic imprinting on quantitative traits |
| Q48258135 | Effects of paternal folate deficiency on the expression of insulin-like growth factor-2 and global DNA methylation in the fetal brain |
| Q34599086 | Elevated expression of H19 and Igf2 in the female mouse eye. |
| Q44043137 | Elevated levels of IGF-1 receptor convey invasive and metastatic capability in a mouse model of pancreatic islet tumorigenesis |
| Q55052972 | Embryological and molecular investigations of parental imprinting on mouse chromosome 7. |
| Q29547452 | Environmental epigenomics and disease susceptibility |
| Q37049211 | Environmental epigenomics in human health and disease |
| Q38263810 | Epigenetic Interactions and Gene Expression in Peri-Implantation Mouse Embryo Development |
| Q36862650 | Epigenetic alteration of imprinted genes during neural differentiation of germline-derived pluripotent stem cells. |
| Q38554712 | Epigenetic alterations in sperm associated with male infertility |
| Q36421376 | Epigenetic and phenotypic consequences of a truncation disrupting the imprinted domain on distal mouse chromosome 7. |
| Q37997894 | Epigenetic aspects on therapy development for gastroenteropancreatic neuroendocrine tumors |
| Q34572727 | Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor |
| Q34347672 | Epigenetic control of the genome-lessons from genomic imprinting |
| Q55506430 | Epigenetic control of variation and stochasticity in metabolic disease. |
| Q73669914 | Epigenetic mark sequence of the H19 gene in human sperm |
| Q35909876 | Epigenetic mechanisms of genomic imprinting: common themes in the regulation of imprinted regions in mammals, plants, and insects |
| Q72094721 | Epigenetic mechanisms underlying the imprinting of the mouse H19 gene |
| Q33678779 | Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome |
| Q38124796 | Epigenetic regulation of genomic imprinting from germ line to preimplantation |
| Q34734556 | Epigenetic regulation of placental endocrine lineages and complications of pregnancy |
| Q38510215 | Epigenetic regulation of stemness maintenance in the neurogenic niches. |
| Q38205048 | Epigenetic regulation of the Igf2/H19 gene cluster |
| Q34391404 | Epigenetics across the human lifespan |
| Q33909693 | Epigenetics and assisted reproductive technology: a call for investigation |
| Q36958186 | Epigenetics and phenotypic variability: some interesting insights from birds |
| Q28730790 | Epigenetics: connecting environment and genotype to phenotype and disease |
| Q37469995 | Epigenetics: definition, mechanisms and clinical perspective. |
| Q52021941 | Establishment and maintenance of H19 imprinting in the germline and preimplantation embryo. |
| Q28297145 | Establishment of functional imprinting of the H19 gene in human developing placentae |
| Q33866151 | Estrogen Receptor-β and the Insulin-Like Growth Factor Axis as Potential Therapeutic Targets for Triple-Negative Breast Cancer. |
| Q51079925 | Estrogen signaling, through estrogen receptor β, regulates DNA methylation and its machinery in male germ line in adult rats. |
| Q36697811 | Estrogens and aspects of prostate disease |
| Q34057784 | Estrogens and prostatic disease. International Prostate Health Council Study Group |
| Q33735829 | Evaluation of allelic expression of imprinted genes in adult human blood. |
| Q55712236 | Evidence for a priming effect on maternal resource allocation: implications for interbrood competition. |
| Q54053029 | Evidence for genomic imprinting of the major QTL controlling susceptibility to trypanosomiasis in mice. |
| Q46538872 | Evolution and Function of the Insulin and Insulin-like Signaling Network in Ectothermic Reptiles: Some Answers and More Questions |
| Q26774995 | Evolution and function of genomic imprinting in plants |
| Q91728093 | Evolution of cis- and trans-regulatory divergence in the chicken genome between two contrasting breeds analyzed using three tissue types at one-day-old |
| Q33338682 | Evolution of the CDKN1C-KCNQ1 imprinted domain |
| Q48082855 | Evolutionary Conflict Between Maternal and Paternal Interests: Integration with Evolutionary Endocrinology |
| Q47441747 | Evolving paradigms for the biological response to low dose ionizing radiation; the role of epigenetics. |
| Q40579171 | Experimental embryological analysis of genetic imprinting in mouse development |
| Q33320359 | Expression and protein localisation of IGF2 in the marsupial placenta |
| Q41140340 | Expression of H19 does not influence the timing of replication of the Igf2/H19 imprinted region |
| Q52211093 | Expression of X-linked genes in androgenetic, gynogenetic, and normal mouse preimplantation embryos. |
| Q82276593 | Expression of a modified H19 RNA does not cause embryonic lethality in mice |
| Q98629483 | Expression of acid-labile subunit (als) in developing and adult zebrafish and its role in dorso-ventral patterning during development |
| Q50794831 | Expression of delta-like 1 homologue and insulin-like growth factor 2 through epigenetic regulation of the genes during development of mouse molar. |
| Q33881937 | Expression of insulin-like growth factor II (IGF)-II) and H19 in murine teratocarcinomas derived from embryonic stem (ES) cells |
| Q36827494 | Expression of mannose 6-phosphate receptors in chicken |
| Q28140831 | Expression of the imprinted H19 oncofetal RNA in epithelial ovarian cancer |
| Q50768825 | Expression patterns of insulin-like growth factor system members and their correlations with growth and carcass traits in Landrace and Lantang pigs during postnatal development. |
| Q61776055 | Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: relation to expression and imprinting |
| Q39456763 | Extraordinary Cancer Epigenomics: Thinking Outside the Classical Coding and Promoter Box. |
| Q38504209 | FISH mapping of the IGF2 gene in horse and donkey-detection of homoeology with HSA11. |
| Q37787567 | Familial predisposition to adrenocortical tumors: Clinical and biological features and management strategies |
| Q34578955 | Fat dads must not be blamed for their children's health problems |
| Q47961972 | Fate of methylated/unmethylated H19 imprinting control region after paternal and maternal pronuclear injection |
| Q46961163 | Female promiscuity and maternally dependent offspring growth rates in mammals. |
| Q38287045 | Focusing on long noncoding RNA dysregulation in gastric cancer |
| Q28505087 | FoxA proteins regulate H19 endoderm enhancer E1 and exhibit developmental changes in enhancer binding in vivo |
| Q28140252 | Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma |
| Q28215251 | Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma |
| Q37865526 | From Waddington's epigenetic landscape to small noncoding RNA: some important milestones in the history of epigenetics research |
| Q33648749 | Functional evaluation of ES-somatic cell hybrids in vitro and in vivo |
| Q37556602 | Functional expression study of igf2 antisense transcript in mouse |
| Q28285950 | Gain of allelic gene expression for IGF-II occurs frequently in Barrett's esophagus |
| Q36251483 | Gametes and embryo epigenetic reprogramming affect developmental outcome: implication for assisted reproductive technologies |
| Q86638498 | Gametic imprinting effects on rate and composition of pig growth |
| Q36552551 | Gene disruption in mammals |
| Q39218499 | Gene expression and regulation in adrenocortical tumorigenesis |
| Q35148461 | Gene expression in pre-implantation mammalian embryos |
| Q41510870 | Gene expression in the rat brain during prostaglandin D2 and adenosinergically-induced sleep. |
| Q41127738 | Gene targeting in kidney development |
| Q36538951 | Gene therapy for colorectal cancer by an oncolytic adenovirus that targets loss of the insulin-like growth factor 2 imprinting system |
| Q36730925 | Gene-environment interactions and epigenetic basis of human diseases |
| Q38094638 | Generating new neurons to circumvent your fears: the role of IGF signaling. |
| Q39003527 | Genetic Studies on Mammalian DNA Methyltransferases |
| Q37961799 | Genetic and epigenetic dysregulation of imprinted genes in the brain |
| Q61693865 | Genetic conflicts and the evolutionary origin of genomic imprinting |
| Q34602685 | Genetic conflicts, multiple paternity and the evolution of genomic imprinting. |
| Q34032271 | Genetic control of intra-uterine growth |
| Q52220346 | Genetic imprinting in the mouse: implications for gene regulation. |
| Q34742989 | Genetic imprinting of H19 and IGF2 in domestic pigs (Sus scrofa). |
| Q72639533 | Genetic mapping and systematic screening of mouse endogenously imprinted loci detected with restriction landmark genome scanning method (RLGS) |
| Q70457181 | Genetic mosaicism in normal tissues of Wilms' tumour patients |
| Q34056811 | Genetically caused retarded growth in animals |
| Q72539974 | Genetics of Wilms' tumor: a blend of aberrant development and genomic imprinting |
| Q27015889 | Genome wide functional genetics in haploid cells |
| Q36436558 | Genome-wide survey of imprinted genes |
| Q33186874 | Genome‐Wide Analysis of Epigenetics in Cancer |
| Q55363193 | Genomic Imprinting and the Regulation of Postnatal Neurogenesis. |
| Q46005770 | Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19. |
| Q36806812 | Genomic imprinting - the story of the other half and the conflicts of silencing. |
| Q77809556 | Genomic imprinting and cancer |
| Q33721384 | Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome |
| Q72872602 | Genomic imprinting and gene activation in cancer |
| Q37769333 | Genomic imprinting and mammalian reproduction. |
| Q34393452 | Genomic imprinting and the maternal brain |
| Q36670037 | Genomic imprinting effects on adult body composition in mice |
| Q34699894 | Genomic imprinting effects on brain development and function |
| Q37715275 | Genomic imprinting in development, growth, behavior and stem cells |
| Q41175197 | Genomic imprinting in disorders of growth |
| Q26828858 | Genomic imprinting in mammals |
| Q21145256 | Genomic imprinting in mammals: emerging themes and established theories |
| Q33918746 | Genomic imprinting in plants: observations and evolutionary implications |
| Q41587298 | Genomic imprinting in the brain |
| Q48003531 | Genomic imprinting is disrupted in interspecific Peromyscus hybrids |
| Q36439829 | Genomic imprinting leads to less selectively maintained polymorphism on X chromosomes |
| Q37710386 | Genomic imprinting mechanisms in embryonic and extraembryonic mouse tissues |
| Q37105077 | Genomic imprinting mechanisms in mammals. |
| Q36421141 | Genomic imprinting of Dopa decarboxylase in heart and reciprocal allelic expression with neighboring Grb10. |
| Q73594889 | Genomic imprinting of IGF2 and H19 in human meningiomas |
| Q38298288 | Genomic imprinting of Mash2, a mouse gene required for trophoblast development |
| Q38291049 | Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse |
| Q34771178 | Genomic imprinting proposed as a surveillance mechanism for chromosome loss |
| Q35212932 | Genomic imprinting, sibling solidairity and the logic of collective action |
| Q35043699 | Genomic imprinting--insights from studies in mice. |
| Q38172016 | Genomic imprinting--the struggle of the genders at the molecular level |
| Q36238495 | Genomic imprinting: antagonistic mechanisms in the germ line and early embryo |
| Q33603375 | Genomic imprinting: concept and clinical consequences |
| Q35037387 | Genomic imprinting: could the chromatin structure be the driving force? |
| Q37068291 | Genomic imprinting: developmental significance and molecular mechanism |
| Q37362832 | Genomic imprinting: employing and avoiding epigenetic processes |
| Q33541538 | Genomic imprinting: implications for human disease |
| Q35833288 | Genomic imprinting: mechanism and role in human pathology |
| Q29616227 | Genomic imprinting: parental influence on the genome |
| Q51860651 | Genomic imprinting: the emergence of an epigenetic paradigm. |
| Q36993617 | Ghrelin and bone. |
| Q37082645 | Global assessment of imprinted gene expression in the bovine conceptus by next generation sequencing |
| Q33687971 | Global gene expression profiling of somatic motor neuron populations with different vulnerability identify molecules and pathways of degeneration and protection |
| Q57791371 | Glypicans: a growing trend |
| Q46333073 | Growth, development, and gene expression by in vivo- and in vitro-produced day 7 and 16 bovine embryos |
| Q50994637 | Gtl2lacZ, an insertional mutation on mouse chromosome 12 with parental origin-dependent phenotype. |
| Q28505457 | Gtx: a novel murine homeobox-containing gene, expressed specifically in glial cells of the brain and germ cells of testis, has a transcriptional repressor activity in vitro for a serum-inducible promoter |
| Q28139674 | H19 RNA binds four molecules of insulin-like growth factor II mRNA-binding protein |
| Q35194017 | H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19. |
| Q44282328 | H19 gene controls placental development through a miRNA |
| Q53900112 | H19 gene expression is up-regulated exclusively by stabilization of the RNA during muscle cell differentiation. |
| Q33648826 | H19 imprinting control region methylation requires an imprinted environment only in the male germ line. |
| Q52208588 | H19 is imprinted in the choroid plexus and leptomeninges of the mouse foetus |
| Q37352630 | H19, a marker of developmental transition, is reexpressed in human atherosclerotic plaques and is regulated by the insulin family of growth factors in cultured rabbit smooth muscle cells |
| Q34245929 | Haploid genomes illustrate epigenetic constraints and gene dosage effects in mammals |
| Q35814612 | High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes |
| Q37421551 | How cohesin and CTCF cooperate in regulating gene expression |
| Q24322948 | Human PEG1/MEST, an imprinted gene on chromosome 7 |
| Q37962006 | Human imprinting syndromes. |
| Q24534008 | Human insulin-like growth factor II leader 2 mediates internal initiation of translation |
| Q80931810 | Hypomethylated and hypermethylated profiles of H19DMR are associated with the aberrant imprinting of IGF2 and H19 in human hepatocellular carcinoma |
| Q48202303 | I-cell disease-like phenotype in mice deficient in mannose 6-phosphate receptors |
| Q34781425 | IGF signaling directs ventricular cardiomyocyte proliferation during embryonic heart development |
| Q44247178 | IGF-2 is a mediator of prolactin-induced morphogenesis in the breast |
| Q28278853 | IGF2 is critical for tumorigenesis by synovial sarcoma oncoprotein SYT-SSX1 |
| Q70765937 | IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome |
| Q92702627 | IGF2/IGF1R Signaling as a Therapeutic Target in MYB-Positive Adenoid Cystic Carcinomas and Other Fusion Gene-Driven Tumors |
| Q36561897 | IGF2: epigenetic regulation and role in development and disease |
| Q92564685 | IGFBP2: integrative hub of developmental and oncogenic signaling network |
| Q42601971 | Identification and characterization of G90, a novel mouse RNA that lacks an extensive open reading frame |
| Q46259020 | Identification and expression analysis of cDNA encoding insulin-like growth factor 2 in horses. |
| Q48060772 | Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M. |
| Q48086267 | Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method |
| Q52211090 | Identification of genes showing altered expression in preimplantation and early postimplantation parthenogenetic embryos. |
| Q35793734 | Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene |
| Q35205921 | Igf2 imprinting does not require its own DNA methylation or H19 RNA. |
| Q36166920 | Igf2 ligand dependency of Pten(+/-) developmental and tumour phenotypes in the mouse |
| Q36386448 | Igf2 pathway dependency of the Trp53 developmental and tumour phenotypes. |
| Q35829427 | Impact of DNA methylation on trophoblast function. |
| Q31032416 | Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins |
| Q52089452 | Implications of cloning technique for reproductive medicine. |
| Q52114528 | Imprint control element-mediated secondary methylation imprints at the Igf2/H19 locus. |
| Q89595427 | Imprinted Maternally Expressed microRNAs Antagonize Paternally Driven Gene Programs in Neurons |
| Q48045480 | Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons |
| Q41066932 | Imprinted genes and regulation of gene expression by epigenetic inheritance. |
| Q34427642 | Imprinted loci in domestic livestock species as epigenomic targets for artificial selection of complex traits. |
| Q51934816 | Imprinting analysis in the Acrodysplasia region of mouse chromosome 12. |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q34402875 | Imprinting and transgenerational modulation of gene expression; human growth as a model |
| Q35213638 | Imprinting errors and developmental asymmetry |
| Q37615120 | Imprinting evolution and human health |
| Q33594945 | Imprinting in Albright's hereditary osteodystrophy |
| Q50958667 | Imprinting is also a mechanism for immediate or delayed hemizygous expression of several uniparental haplotypes selected from the genome of each sex. |
| Q48096674 | Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human. |
| Q35194604 | Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching |
| Q24568014 | Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15 |
| Q39733758 | Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites. |
| Q36436488 | Imprinting today: end of the beginning or beginning of the end? |
| Q35025123 | In utero exposure to cigarette chemicals induces sex-specific disruption of one-carbon metabolism and DNA methylation in the human fetal liver |
| Q50888205 | In vitro and early in vivo development of sheep gynogenones and putative androgenones. |
| Q37080106 | In vivo and in vitro differentiation of uniparental embryonic stem cells into hematopoietic and neural cell types |
| Q46816817 | Inactivation of the IGF-I gene in mice results in perinatal lethality |
| Q36969422 | Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome |
| Q52572805 | Independent regulation of skeletal growth by Ihh and IGF signaling. |
| Q34151298 | Influence of in vitro systems on embryo survival and fetal development in cattle |
| Q35038492 | Influence of mom and dad: quantitative genetic models for maternal effects and genomic imprinting |
| Q73786615 | Inhibition of mammary epithelial apoptosis and sustained phosphorylation of Akt/PKB in MMTV-IGF-II transgenic mice |
| Q35818573 | Insulin Like Growth Factor 2 Expression in the Rat Brain Both in Basal Condition and following Learning Predominantly Derives from the Maternal Allele |
| Q33911127 | Insulin and IGF receptor signalling in neural-stem-cell homeostasis. |
| Q57384414 | Insulin is imprinted in the placenta of the marsupial, Macropus eugenii |
| Q56524301 | Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility |
| Q40485317 | Insulin-like Growth Factor Binding Proteins |
| Q64068201 | Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine |
| Q35229856 | Insulin-like growth factor 2 (IGF-2) potentiates BMP-9-induced osteogenic differentiation and bone formation |
| Q54745902 | Insulin-like growth factor 2 expressed in a novel fetal liver cell population is a growth factor for hematopoietic stem cells |
| Q41377136 | Insulin-like growth factor 2 modulates murine hematopoietic stem cell maintenance through upregulation of p57. |
| Q28281165 | Insulin-like growth factor II (IGF-II) |
| Q46773559 | Insulin-like growth factor II acts through an endogenous growth pathway regulated by imprinting in early mouse embryos |
| Q33904097 | Insulin-like growth factor binding proteins: IGF-dependent and -independent effects in the mammary gland |
| Q40607017 | Insulin-like growth factor mediated stromal-epithelial interactions in human breast cancer |
| Q42396741 | Insulin-like growth factor receptor 1b is required for zebrafish primordial germ cell migration and survival |
| Q34074077 | Insulin-like growth factor regulates peak bone mineral density in mice by both growth hormone-dependent and -independent mechanisms |
| Q46364420 | Insulin-like growth factor signaling regulates developmental trajectory associated with diapause in embryos of the annual killifish Austrofundulus limnaeus. |
| Q74372350 | Insulin-like growth factor-II imprinting in cancer |
| Q39214150 | Insulin-like growth factor-II is produced by, signals to and is an important survival factor for the mature podocyte in man and mouse. |
| Q28352298 | Insulin-like growth factors I and II induce cell death in Wilms's tumour cells |
| Q41175220 | Insulin-like growth factors and their receptors in growth |
| Q41565497 | Insulin-like growth factors in poultry. |
| Q52329568 | Insulin-like growth factors: actions on the skeleton. |
| Q64931810 | Intergenic and intronic DNA hypomethylated regions as putative regulators of imprinted domains. |
| Q53986584 | Intragenomic conflict and cancer. |
| Q46802680 | Intragenomic conflict and the evolution of eusociality |
| Q36436520 | Intragenomic politics |
| Q30422328 | Introduction of a point mutation into the mouse genome by homologous recombination in embryonic stem cells using a replacement type vector with a selectable marker |
| Q34511692 | Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring |
| Q77618451 | Involvement of IGF2 and H19 imprinting in choriocarcinoma development |
| Q37704785 | Isolation and characterization of novel pituitary tumor related genes: a cDNA representational difference approach |
| Q42505074 | IκB kinase/nuclear factor κB-dependent insulin-like growth factor 2 (Igf2) expression regulates synapse formation and spine maturation via Igf2 receptor signaling. |
| Q39631819 | Kin conflict in insect societies: a new epigenetic perspective. |
| Q49012032 | Lack of imprinting of the human dopamine D4 receptor (DRD4) gene |
| Q37378662 | Large offspring syndrome: a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann. |
| Q42664271 | Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome. |
| Q36436563 | Lessons from comparative analysis of species-specific imprinted genes. |
| Q41231379 | Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay |
| Q34385827 | Long range interactions regulate Igf2 gene transcription during skeletal muscle differentiation |
| Q40021441 | Long-range RNA interaction of two sequence elements required for endonucleolytic cleavage of human insulin-like growth factor II mRNAs. |
| Q28506802 | Loss of Cited2 affects trophoblast formation and vascularization of the mouse placenta |
| Q33630697 | Loss of IGF2 imprinting is associated with abrogation of long-range intrachromosomal interactions in human cancer cells |
| Q47102226 | Loss of imprinting mutations define both distinct and overlapping roles for misexpression of IGF2 and of H19 lncRNA. |
| Q36813932 | Loss of imprinting of IGF2 and the epigenetic progenitor model of cancer |
| Q72703028 | Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour |
| Q28594559 | Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans |
| Q55034610 | Lost in translation: The 3'-UTR of IGF1R as an ancient long noncoding RNA. |
| Q33908331 | M6P/IGF2R imprinting evolution in mammals |
| Q92002429 | MEG3-derived miR-493-5p overcomes the oncogenic feature of IGF2-miR-483 loss of imprinting in hepatic cancer cells |
| Q72525432 | MHC class I genes are not imprinted in the mouse placenta |
| Q38012332 | Macro lncRNAs: a new layer of cis-regulatory information in the mammalian genome |
| Q54311182 | Maintenance of feeder free anchorage independent cultures of ES and iPS cells by retinol/vitamin A. |
| Q33294657 | Maintenance of paternal methylation and repression of the imprinted H19 gene requires MBD3 |
| Q34026917 | Mammalian genomic imprinting. |
| Q28603472 | Mammalian-specific genomic functions: Newly acquired traits generated by genomic imprinting and LTR retrotransposon-derived genes in mammals |
| Q51976586 | Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development. |
| Q96230919 | Maternal H3K27me3-dependent autosomal and X chromosome imprinting |
| Q45103962 | Maternal administration of the herbal medicine toki-shakuyaku-san promotes fetal growth and placental gene expression in normal mice |
| Q67510275 | Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression |
| Q48628193 | Maternal diabetes causes alterations of DNA methylation statuses of some imprinted genes in murine oocytes |
| Q37497577 | Maternal imprinting at the H19-Igf2 locus maintains adult haematopoietic stem cell quiescence. |
| Q24305283 | Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome |
| Q44185908 | Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region |
| Q43802401 | Maternal primary imprinting is established at a specific time for each gene throughout oocyte growth |
| Q34611930 | Maternal transmission of a humanised Igf2r allele results in an Igf2 dependent hypomorphic and non-viable growth phenotype |
| Q37336786 | Maternal vitamin D depletion alters DNA methylation at imprinted loci in multiple generations |
| Q35065101 | Maternal-placental-fetal interactions in the endocrine regulation of fetal growth: role of somatotrophic axes. |
| Q28511059 | Matrix metalloproteinase-9 maps to the distal end of chromosome 2 in the mouse |
| Q38503402 | Matrix-attachment regions in the mouse chromosome 7F imprinted domain |
| Q74312289 | Mechanisms of genomic imprinting |
| Q40575113 | Mechanisms of genomic imprinting in mammals |
| Q35623181 | Mechanisms of insulator function in gene regulation and genomic imprinting |
| Q40413626 | Mechanistic and developmental aspects of genetic imprinting in mammals |
| Q34345380 | Mechanistic aspects of genome-wide demethylation in the preimplantation mouse embryo |
| Q24611482 | Mediation of CTCF transcriptional insulation by DEAD-box RNA-binding protein p68 and steroid receptor RNA activator SRA |
| Q34750294 | Metastable epialleles in mammals |
| Q35156096 | Methods for detecting interactions between imprinted genes and environmental exposures using birth cohort designs with mother-offspring pairs |
| Q34363070 | Methylation and imprinting: from host defense to gene regulation? |
| Q72164123 | Methylation imprinting was observed of mouse mo-2 macrosatellite on the pseudoautosomal region but not on chromosome 9 |
| Q28145754 | Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene |
| Q48691224 | Methylation status in the intragenic differentially methylated region of the IGF2 locus in Bos taurus indicus oocytes with different developmental competencies |
| Q60060443 | Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r) |
| Q34634361 | MicroRNA profiling of adrenocortical tumors reveals miR-483 as a marker of malignancy |
| Q40468269 | Molecular Genetics and Cytogenetics of Sarcomas |
| Q40383506 | Molecular advances in pediatric urology |
| Q67521534 | Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11 |
| Q40807181 | Molecular biology for the pediatric surgeon |
| Q40922422 | Molecular biology of testicular germ cell tumors: current status |
| Q35979181 | Molecular genetic analysis of chromosome 11p in familial Wilms tumour |
| Q35088684 | Molecular links between X-inactivation and autosomal imprinting: X-inactivation as a driving force for the evolution of imprinting? |
| Q28184725 | Monoallelic expression of the human H19 gene |
| Q34085483 | Monotreme IGF2 expression and ancestral origin of genomic imprinting |
| Q36888462 | Mosaic analysis with double markers reveals cell-type-specific paternal growth dominance. |
| Q48084685 | Mosaic and polymorphic imprinting of the WT1 gene in humans |
| Q33675226 | Mosaic uniparental disomy in Beckwith-Wiedemann syndrome. |
| Q35675706 | Mouse chromosome 7. |
| Q40533324 | Mouse genetics in the 21st century: using gene targeting to create a cornucopia of mouse mutants possessing precise genetic modifications |
| Q30495383 | Mouse homologues of human hereditary disease. |
| Q35197831 | Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes |
| Q42989736 | Mouse mutants lacking the cation-independent mannose 6-phosphate/insulin-like growth factor II receptor are impaired in lysosomal enzyme transport: comparison of cation-independent and cation-dependent mannose 6-phosphate receptor-deficient mice |
| Q34276674 | Natural Selection and the Evolution of Genome Imprinting |
| Q33927035 | Natural selection and the function of genome imprinting: beyond the silenced minority |
| Q37183028 | Neurogenesis at the brain-cerebrospinal fluid interface |
| Q37445958 | New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain |
| Q26852971 | New insights into establishment and maintenance of DNA methylation imprints in mammals |
| Q35688004 | Next-Generation Sequencing Techniques Reveal that Genomic Imprinting Is Absent in Day-Old Gallus gallus domesticus Brains. |
| Q33493060 | No evidence for mutations of CTCFL/BORIS in Silver-Russell syndrome patients with IGF2/H19 imprinting control region 1 hypomethylation |
| Q37917894 | Non-coding RNA and antisense RNA. Nature's trash or treasure? |
| Q37417123 | Non-coding RNAs and the acquisition of genomic imprinting in mammals. |
| Q34801141 | Non-coding ribonucleic acids--a class of their own? |
| Q91846314 | Nonclassical GH Insensitivity: Characterization of Mild Abnormalities of GH Action |
| Q36872209 | Noncoding RNAs and RNA editing in brain development, functional diversification, and neurological disease |
| Q35074463 | Novel cis-regulatory function in ICR-mediated imprinted repression of H19 |
| Q26823935 | Nuclear lncRNAs as epigenetic regulators-beyond skepticism |
| Q52220644 | Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma. |
| Q51545297 | Ontogeny of the H19 gene in sheep and effect of maternal fasting on its expression in the fetus. |
| Q35194803 | Oppositely imprinted genes H19 and insulin-like growth factor 2 are coexpressed in human androgenetic trophoblast |
| Q35209963 | Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome |
| Q39018235 | Origin and evolution of the metazoan non-coding regulatory genome |
| Q37339103 | Overgrowth disorders associated with tall stature |
| Q84796427 | Overview of Mammalian Genome special issue on epigenetics |
| Q54046794 | Ovine surfactant protein cDNAs: use in studies on fetal lung growth and maturation after prolonged hypoxemia. |
| Q42676599 | PCR-cloning and gene expression studies in common carp (Cyprinus carpio) insulin-like growth factor-II. |
| Q43859963 | Parametric proportional hazards model for mapping genomic imprinting of survival traits |
| Q35133737 | Parent-of-origin effects implicate epigenetic regulation of experimental autoimmune encephalomyelitis and identify imprinted Dlk1 as a novel risk gene. |
| Q24672503 | Parent-of-origin effects in multiple endocrine neoplasia type 2B |
| Q37372380 | Parent-of-origin effects on cardiac response to pressure overload in mice |
| Q34659444 | Parent-of-origin specific QTL--a possibility towards understanding reciprocal effects in chicken and the origin of imprinting |
| Q33595266 | Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome |
| Q24673085 | Parental antagonism, relatedness asymmetries, and genomic imprinting |
| Q72222239 | Parental genomic imprinting of the human IGF2 gene |
| Q40672445 | Parental imprinting of autosomal mammalian genes |
| Q46725382 | Parental imprinting of the Mas protooncogene in mouse |
| Q28187996 | Parental imprinting of the human H19 gene |
| Q22122365 | Parental imprinting of the mouse H19 gene |
| Q49161161 | Parental methylation patterns of a transgenic locus in adult somatic tissues are imprinted during gametogenesis |
| Q33596161 | Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy. |
| Q33674736 | Parental origin of transcription from the human GNAS1 gene. |
| Q34363043 | Parental-origin-specific epigenetic modification of the mouse H19 gene |
| Q68244654 | Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis |
| Q46442933 | Parent‐specific expression of a human keratin 18/β‐galactosidase fusion gene in transgenic mice |
| Q38852159 | Parsimonious model for analyzing parent-of-origin effects related to beef traits in dual-purpose Simmental |
| Q35196278 | Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus |
| Q55475439 | Patched target Igf2 is indispensable for the formation of medulloblastoma and rhabdomyosarcoma. |
| Q37584284 | Paternal Insulin-like Growth Factor 2 (Igf2) Regulates Stem Cell Activity During Adulthood. |
| Q77493342 | Paternal age affects fertility and progeny outcome in the Brown Norway rat |
| Q72007860 | Paternal and maternal major histocompatibility complex class I antigens are expressed co-dominantly by equine trophoblast |
| Q52197507 | Paternal repression of the imprinted mouse Igf2r locus occurs during implantation and is stable in all tissues of the post-implantation mouse embryo. |
| Q28593512 | Paternal versus maternal transmission of a stimulatory G-protein alpha subunit knockout produces opposite effects on energy metabolism |
| Q36967749 | Paternally expressed genes predominate in the placenta. |
| Q33679562 | Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome |
| Q33872476 | Pathogenesis of adrenocortical incidentalomas and genetic syndromes associated with adrenocortical neoplasms |
| Q34597093 | Pathologic features and expression of insulin-like growth factor-2 in adrenocortical neoplasms |
| Q48104557 | Pathology of the adrenal cortex: a reappraisal of the past 25 years focusing on adrenal cortical tumors. |
| Q73195361 | Patterns in expression of insulin-like growth factor-II and of proliferative activity in the normal human first and third trimester placenta demonstrated by non-isotopic in situ hybridization and immunohistochemical staining for MIB-1 |
| Q42121426 | Paxillin-dependent regulation of IGF2 and H19 gene cluster expression |
| Q48071136 | Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization |
| Q34634517 | Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse. |
| Q37712366 | Perturbations to the IGF1 growth pathway and adult energy homeostasis following disruption of mouse chromosome 12 imprinting. |
| Q35136430 | Phenotypic consequences of deletion of the gamma 3, alpha 5, or beta 3 subunit of the type A gamma-aminobutyric acid receptor in mice |
| Q28588859 | Phosphatidylinositol 3-kinase (PI3K) signaling via glycogen synthase kinase-3 (Gsk-3) regulates DNA methylation of imprinted loci |
| Q37496159 | Phylogenetic footprint analysis of IGF2 in extant mammals |
| Q31158518 | Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2 |
| Q33271303 | Physical mapping of the IGF2 locus in the South American opossum Monodelphis domestica |
| Q74453906 | Pituitary Insulin: Insulin-Like Growth Factors |
| Q36414579 | Placental glycogen stores are increased in mice with H19 null mutations but not in those with insulin or IGF type 1 receptor mutations |
| Q24530568 | Placental overgrowth in mice lacking the imprinted gene Ipl |
| Q38880458 | Placental phenotype and the insulin-like growth factors: resource allocation to fetal growth. |
| Q47844221 | Placental programming of anxiety in adulthood revealed by Igf2-null models. |
| Q51320374 | Placental-Specific Overexpression of sFlt-1 Alters Trophoblast Differentiation and Nutrient Transporter Expression in an IUGR Mouse Model. |
| Q34135795 | Placental-specific IGF-II is a major modulator of placental and fetal growth. |
| Q34332616 | Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta |
| Q48400038 | Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain |
| Q53427610 | Polymorphisms, genomic imprinting and cancer susceptibility. |
| Q34608309 | Population models of genomic imprinting. I. Differential viability in the sexes and the analogy with genetic dominance |
| Q35038510 | Population models of genomic imprinting. II. Maternal and fertility selection |
| Q28655490 | Post-natal imprinting: evidence from marsupials |
| Q41026364 | Post-translational processing of the insulin-like growth factor-2 precursor. Analysis of O-glycosylation and endoproteolysis |
| Q33523010 | Postnatal survival of mice with maternal duplication of distal chromosome 7 induced by a Igf2/H19 imprinting control region lacking insulator function |
| Q45767257 | Preferential loss of heterozygosity of chromosome 7 loci in simian virus 40 t/T antigen-induced mouse hepatocellular carcinomas does not involve H-ras mutations. |
| Q64053408 | Prenatal epigenetics diets play protective roles against environmental pollution |
| Q33213351 | Profiling of oxygen-modulated gene expression in early human placenta by systematic sequencing of suppressive subtractive hybridization products |
| Q48569804 | Proliferation and differentiation of androgenetic cells in fetal mouse chimeras |
| Q44060508 | Proliferation and growth factor expression in abnormally enlarged placentas of mouse interspecific hybrids |
| Q36402949 | Promiscuous gene expression in thymic epithelial cells is regulated at multiple levels |
| Q34358824 | Promoter-specific expression and imprint status of marsupial IGF2 |
| Q34445469 | Promoter-specific expression of the imprinted IGF2 gene in cattle (Bos taurus). |
| Q46095293 | Promoter-specific imprinting of the human insulin-like growth factor-II gene |
| Q77129209 | Promoter-specific insulin-like growth factor 2 gene imprinting in human fetal liver and hepatoblastoma |
| Q45985336 | Promoter-specific modulation of insulin-like growth factor II genomic imprinting by inhibitors of DNA methylation. |
| Q35904778 | Quantitative Genetics Identifies Cryptic Genetic Variation Involved in the Paternal Regulation of Seed Development |
| Q35746705 | Quantitative genetics of genomic imprinting: a comparison of simple variance derivations, the effects of inbreeding, and response to selection |
| Q34301920 | RACK1 recruits STAT3 specifically to insulin and insulin-like growth factor 1 receptors for activation, which is important for regulating anchorage-independent growth |
| Q38600684 | Random monoallelic expression of autosomal genes: stochastic transcription and allele-level regulation |
| Q36882519 | Rapidly generating knockout mice from H19-Igf2 engineered androgenetic haploid embryonic stem cells |
| Q34412090 | Re-expression of IGF-II is important for beta cell regeneration in adult mice |
| Q92640261 | Recapitulation of gametic DNA methylation and its post-fertilization maintenance with reassembled DNA elements at the mouse Igf2/H19 locus |
| Q37833397 | Regulation and flexibility of genomic imprinting during seed development |
| Q28083996 | Regulation of Long Bone Growth in Vertebrates; It Is Time to Catch Up |
| Q24548607 | Regulation of X-chromosome inactivation in development in mice and humans |
| Q52191441 | Regulation of a promoter from the mouse insulin like growth factor II gene by glucocorticoids. |
| Q41415190 | Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene |
| Q36436592 | Regulation of growth and metabolism by imprinted genes |
| Q33760043 | Regulation of imprinted expression by macro non-coding RNAs |
| Q37087590 | Regulation of imprinting in clusters: noncoding RNAs versus insulators |
| Q36734567 | Regulation of skeletal growth and mineral acquisition by the GH/IGF-1 axis: Lessons from mouse models. |
| Q35058363 | Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. |
| Q33901690 | Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2. |
| Q52545355 | Relaxation of imprinted genes in human cancer. |
| Q59088779 | Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour |
| Q34426502 | Reprogramming of genome function through epigenetic inheritance |
| Q45265601 | Restricted development of mouse triploid fetuses with disorganized expression of imprinted genes |
| Q34022943 | Retrotransposition and genomic imprinting |
| Q33612954 | Review paper: origin and molecular pathology of adrenocortical neoplasms |
| Q29618669 | Role for DNA methylation in genomic imprinting |
| Q37338436 | Role of ART in imprinting disorders |
| Q47328314 | Role of H19 3' sequences in controlling H19 and Igf2 imprinting and expression |
| Q41685042 | Role of imprinting in abnormal human development |
| Q24534366 | Role of pro-IGF-II processing by proprotein convertase 4 in human placental development |
| Q45901728 | SNP and haplotype analysis reveal IGF2 variants associated with growth traits in Chinese Qinchuan cattle. |
| Q36411455 | Selected imprinting of INS in the marsupial |
| Q33596012 | Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5). |
| Q33886215 | Short interspersed element (SINE) depletion and long interspersed element (LINE) abundance are not features universally required for imprinting |
| Q33897588 | Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome |
| Q67482929 | Signs of an imprinted domain |
| Q59032284 | Silence of the genes |
| Q52618444 | Similarity and Variation in the Insulin-like Growth Factor 2 - H19 Locus in Primates. |
| Q55053406 | Single nucleotide polymorphisms at the imprinted bovine insulin-like growth factor 2 (IGF2) locus are associated with dairy performance in Irish Holstein-Friesian cattle. |
| Q52228211 | Site of action of imprinted genes revealed by phenotypic analysis of parthenogenetic embryos. |
| Q33694153 | Sperm nuclear activation during fertilization. |
| Q54911446 | Stage dependent nutritional regulation of transgenerational longevity. |
| Q28141832 | Steroid hormones modulate H19 gene expression in both mammary gland and uterus |
| Q41844735 | Structural analysis of the human insulin-like growth factor-II P3 promoter |
| Q58201304 | Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus |
| Q28298778 | Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders |
| Q34581769 | Targeted tumor gene therapy based on loss of IGF2 imprinting |
| Q42226751 | Targeting H19, an Imprinted Long Non-Coding RNA, in Hepatic Functions and Liver Diseases |
| Q36383365 | Targeting insulin-like growth factor pathways. |
| Q40427854 | Targeting the mouse genome: a compendium of knockouts (part II) |
| Q64929446 | Technical advances contribute to the study of genomic imprinting. |
| Q52231531 | Teratogenic effects of parthenogenetic cells from LTXBO mice, a strain which develops ovarian teratomas at high frequency. |
| Q47069117 | Tests for parental imprinting in the nematode Caenorhabditis elegans |
| Q57086585 | The 3′ portion of the mouse H19 Imprinting-Control Region is required for proper tissue-specific expression of the Igf2 gene |
| Q38738049 | The Choroid Plexus in Healthy and Diseased Brain |
| Q35201020 | The Dlk1 and Gtl2 genes are linked and reciprocally imprinted |
| Q57153351 | The Epigenetics of Metabolic Syndrome |
| Q37424408 | The H19 differentially methylated region marks the parental origin of a heterologous locus without gametic DNA methylation |
| Q28508794 | The H19 locus acts in vivo as a tumor suppressor |
| Q53944621 | The H19 transcript is associated with polysomes and may regulate IGF2 expression in trans. |
| Q35036870 | The IGFI receptor gene: a molecular target for disrupted transcription factors |
| Q24318274 | The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis |
| Q39251814 | The Igf2as transcript is exported into cytoplasm and associated with polysomes |
| Q90041392 | The Insulin/IGF System in Mammalian Sexual Development and Reproduction |
| Q35848729 | The X chromosome in development in mouse and man |
| Q33994222 | The absence of enhancer competition between Igf2 and H19 following transfer into differentiated cells |
| Q48090298 | The bovine IGF2 gene is differentially methylated in oocyte and sperm DNA. |
| Q35833841 | The cell type-specific IGF2 expression during early human development correlates to the pattern of overgrowth and neoplasia in the Beckwith-Wiedemann syndrome. |
| Q37993422 | The cerebrospinal fluid: regulator of neurogenesis, behavior, and beyond |
| Q36339251 | The choroid plexus-cerebrospinal fluid system: from development to aging. |
| Q50134100 | The complex genetics of human insulin-like growth factor 2 are not reflected in public databases |
| Q50875072 | The conflict theory of genomic imprinting: how much can be explained? |
| Q57086589 | The continuing quest to comprehend genomic imprinting |
| Q34615144 | The correlation between relatives on the supposition of genomic imprinting |
| Q73115464 | The development of preimplantation mouse parthenogenones in vitro in absence of glucose: influence of the maternally inherited components |
| Q57802475 | The discovery and importance of genomic imprinting |
| Q41236736 | The early intracellular signaling pathway for the insulin/insulin-like growth factor receptor family in the mammalian central nervous system |
| Q34643086 | The effect of genetic conflict on genomic imprinting and modification of expression at a sex-linked locus |
| Q36081294 | The effect of parental imprinting on the INS-IGF2 locus of Korean type I diabetic patients |
| Q35771472 | The effect of preconception paternal alcohol exposure on epigenetic remodeling of the h19 and rasgrf1 imprinting control regions in mouse offspring |
| Q35147654 | The emerging role of insulin-like growth factors in testis development and function |
| Q34446112 | The epigenetic basis of gender in flowering plants and mammals |
| Q33366534 | The evolution of epigenetic regulators CTCF and BORIS/CTCFL in amniotes |
| Q33968784 | The evolution of genomic imprinting. |
| Q38779863 | The evolving landscape of imprinted genes in humans and mice: Conflict among alleles, genes, tissues, and kin. |
| Q29617273 | The history of cancer epigenetics |
| Q36931989 | The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility |
| Q43489034 | The human insulin superfamily of polypeptide hormones |
| Q62059578 | The human/mouse imprinted genesIGF2, H19, SNRPN andZNF127 map to two conserved autosomal clusters in a marsupial |
| Q33628787 | The importance of imprinting in the human placenta. |
| Q28512597 | The imprinted Phlda2 gene regulates extraembryonic energy stores |
| Q34236353 | The imprinted brain: how genes set the balance between autism and psychosis |
| Q57050199 | The imprinted gene Pw1/Peg3 regulates skeletal muscle growth, satellite cell metabolic state, and self-renewal |
| Q53001244 | The imprinted mouse Igf2r/Air cluster--a model maternal imprinting system. |
| Q36088917 | The influence of non-coding RNAs on allele-specific gene expression in mammals |
| Q93103675 | The insulin-like growth factor 2 gene in mammals: Organizational complexity within a conserved locus |
| Q37307864 | The insulin-like growth factor system and its receptors: A potential novel anticancer target |
| Q58061470 | The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans |
| Q37278762 | The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann region |
| Q34241071 | The marks, mechanisms and memory of epigenetic states in mammals |
| Q36893343 | The maternal to zygotic transition in mammals |
| Q41175237 | The mechanisms by which growth hormone brings about growth. The relative contributions of growth hormone and insulin-like growth factors |
| Q35223922 | The molecular and cellular biology of insulin-like growth factor II |
| Q28972447 | The molecular basis of genetic dominance |
| Q40801112 | The molecular genetics of Wilms tumor. |
| Q28594499 | The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA |
| Q73208039 | The mouse chromosome 7 distal imprinting domain maps to G-bands F4/F5 |
| Q35716468 | The mouse genome: an overview |
| Q67980512 | The murine leukemia inhibition factor gene (Lif) is located on proximal chromosome 11, not chromosome 13 |
| Q40549915 | The new human genetics |
| Q34059933 | The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. |
| Q27007861 | The origin and evolution of genomic imprinting and viviparity in mammals |
| Q37284688 | The placental imprintome and imprinted gene function in the trophoblast glycogen cell lineage |
| Q37022907 | The prevalence of loss of imprinting of H19 and IGF2 at birth. |
| Q24609254 | The product of the imprinted H19 gene is an oncofetal RNA |
| Q34426232 | The role of genomic imprinting in biology and disease: an expanding view |
| Q35295496 | The role of imprinted genes in fetal growth abnormalities |
| Q37733830 | The role of imprinted genes in mediating susceptibility to neuropsychiatric disorders. |
| Q37608512 | The role of insulin-like growth factor during a postischemic period - new insights into pathophysiologic pathways in cardiac tissue |
| Q35150730 | The role of insulin-like growth factors and IGF-binding proteins in the physiological and pathological processes of the kidney |
| Q41035980 | The role of the insulin-like growth factor system in human cancer |
| Q72017438 | The search for imprinted genes |
| Q35934507 | The structural H19 gene is required for transgene imprinting |
| Q54941492 | The tempo of human childhood: a maternal foot on the accelerator, a paternal foot on the brake. |
| Q41910878 | The transcriptional status but not the imprinting control region determines allele-specific histone modifications at the imprinted H19 locus |
| Q72296658 | The use of restriction landmark genomic scanning to scan the mouse genome for endogenous loci with imprinted patterns of methylation |
| Q28207541 | Thioredoxin post-transcriptional regulation by H19 provides a new function to mRNA-like non-coding RNA |
| Q71441501 | Time of initiation and site of action of the mouse chromosome 11 imprinting effects |
| Q48569829 | Tissue specific loss of proliferative capacity of parthenogenetic cells in fetal mouse chimeras |
| Q48337080 | Tissue-, sex-, and age-specific DNA methylation of rat glucocorticoid receptor gene promoter and insulin-like growth factor 2 imprinting control region |
| Q36548056 | Tissue-specific relationship of S-adenosylhomocysteine with allele-specific H19/Igf2 methylation and imprinting in mice with hyperhomocysteinemia |
| Q36028194 | Towards an understanding of Wilms' tumour. |
| Q41066237 | Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. |
| Q40406568 | Transactivation of mouse insulin-like growth factor II (IGF-II) gene promoters by the AP-1 complex. |
| Q52180058 | Transcriptional regulation and biological significance of the insulin like growth factor II gene. |
| Q33389173 | Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain |
| Q38634732 | Transgenerational epigenetic inheritance of diabetes risk as a consequence of early nutritional imbalances |
| Q35902835 | Transgenerational glucose intolerance with Igf2/H19 epigenetic alterations in mouse islet induced by intrauterine hyperglycemia |
| Q40845596 | Transgenic animals in endocrinological investigation |
| Q35228808 | Transgenic approaches to modifying cell and tissue function |
| Q35910635 | Transgenic epigenetics: using transgenic organisms to examine epigenetic phenomena |
| Q33683075 | Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humans |
| Q37134252 | Trends in human birth weight across two successive generations |
| Q48652732 | Trim28 is required for epigenetic stability during mouse oocyte to embryo transition. |
| Q30499489 | Tumor-suppressor genes: cardinal factors in inherited predisposition to human cancers |
| Q53024647 | Two-dimensional electrophoretic protein patterns of reciprocal hybrids of the mouse strains DBA and C57BL |
| Q24311799 | UBE3A/E6-AP mutations cause Angelman syndrome |
| Q71989840 | Ubiquitous expression and imprinting of Snrpn in the mouse |
| Q93189824 | Understanding Cancer Through the Lens of Epigenetic Inheritance, Allele-Specific Gene Expression, and High-Throughput Technology |
| Q34250734 | Understanding transgenerational epigenetic inheritance via the gametes in mammals |
| Q40549875 | Uniparental disomy and genomic imprinting as causes of human genetic disease |
| Q37207358 | Up-Regulation of microRNA-210 is Associated with Spermatogenesis by Targeting IGF2 in Male Infertility |
| Q41697749 | Upregulation of IGF2 expression during vascular calcification |
| Q36214949 | Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene |
| Q33883551 | Variable imprinting of the heterotrimeric G protein G(s) alpha-subunit within different segments of the nephron |
| Q33338342 | What good is genomic imprinting: the function of parent-specific gene expression |
| Q34030740 | What is the function of IGF-II in postnatal life? Answers from transgenic mouse models. |
| Q36552252 | Yeast silencers can act as orientation-dependent gene inactivation centers that respond to environmental signals |
| Q35181658 | Yy1 gene dosage effect and bi-allelic expression of Peg3. |
| Q30856368 | Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines |
| Q73563096 | [Parental genomic imprinting and its implications in growth] |
| Q51544300 | [Screening of metastasis-related microRNAs in the large-cell lung cancer cell lines with different metastastic potentials]. |
| Q54216111 | c-Myc-induced, long, noncoding H19 affects cell proliferation and predicts a poor prognosis in patients with gastric cancer. |
| Q36500326 | c.A2456C-substitution in Pck1 changes the enzyme kinetic and functional properties modifying fat distribution in pigs. |
| Q92515229 | rs10732516 polymorphism at the IGF2/H19 locus associates with a genotype-specific trend in placental DNA methylation and head circumference of prenatally alcohol-exposed newborns |
| Q55354109 | rs10732516 polymorphism at the IGF2/H19 locus associates with genotype-specific effects on placental DNA methylation and birth weight of newborns conceived by assisted reproductive technology. |