| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1015752579 |
| P356 | DOI | 10.1038/351667A0 |
| P698 | PubMed publication ID | 2052093 |
| P2093 | author name string | Surani MA | |
| Cattanach BM | |||
| Ferguson-Smith AC | |||
| Barton SC | |||
| Beechey CV | |||
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| Insulin-like growth factor 2 and short-range stimulatory loops in control of human placental growth | Q33569080 | ||
| Immunosurgery of mouse blastocyst | Q33925408 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Genomic imprinting and genetic disorders in man. | Q38753070 | ||
| Differential imprinting and expression of maternal and paternal genomes | Q39569895 | ||
| Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting | Q41727650 | ||
| Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons | Q42615815 | ||
| A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. | Q52241373 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Genome imprinting phenomena on mouse chromosome 7 | Q68650344 | ||
| Meiotic disjunction in mouse translocations and the determination of centromere position | Q70712255 | ||
| A simplified method for mouse blastocyst injection | Q71435509 | ||
| P433 | issue | 6328 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 667-670 | |
| P577 | publication date | 1991-06-01 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Embryological and molecular investigations of parental imprinting on mouse chromosome 7. | |
| P478 | volume | 351 |
| Q53691358 | "Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndrome. |
| Q67482957 | A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression |
| Q33287220 | A role for Insulin-like growth factor 2 in specification of the fast skeletal muscle fibre |
| Q46050836 | A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis |
| 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 |
| Q72410823 | Androgenesis and gynogenesis are not causative in early pregnancy loss in humans |
| Q72819474 | Beckwith-Wiedemann syndrome |
| 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 |
| Q33285306 | Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. |
| Q41387004 | Chromatin structure and imprinting: developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene. |
| Q35077074 | Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation. |
| 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. |
| Q33691538 | Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality |
| Q37635469 | Concise review: parthenote stem cells for regenerative medicine: genetic, epigenetic, and developmental features |
| Q24337027 | Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism |
| Q21563370 | Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective |
| Q34378421 | DNA methylation in genomic imprinting, development, and disease |
| Q49380518 | DNA-Methylation: Master or Slave of Neural Fate Decisions? |
| Q45239557 | Dads and disomy and disease |
| Q52165136 | Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12. |
| Q46146329 | Deregulation of both imprinted and expressed alleles of the insulin–like growth factor 2 gene during β–cell tumorigenesis |
| 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 |
| Q46148910 | Disproportional effects of Igf2 knockout on placental morphology and diffusional exchange characteristics in the mouse. |
| Q35850859 | Disproportionate growth in mice with Igf-2 transgenes |
| Q41523994 | Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome |
| Q48569816 | Distribution of androgenetic cells in fetal mouse chimeras |
| Q52128191 | Dynamic temporal and spatial regulation of the cdk inhibitor p57(kip2) during embryo morphogenesis. |
| Q44043137 | Elevated levels of IGF-1 receptor convey invasive and metastatic capability in a mouse model of pancreatic islet tumorigenesis |
| Q39659149 | Epigenetic Differences between Embryonic Stem Cells Generated from Blastocysts DevelopedIn VitroandIn Vivo |
| Q34572727 | Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor |
| Q38124796 | Epigenetic regulation of genomic imprinting from germ line to preimplantation |
| Q26742131 | Epigenetics and inheritance of phenotype variation in livestock |
| Q28297145 | Establishment of functional imprinting of the H19 gene in human developing placentae |
| Q36762442 | Evidence that Igf2 down-regulation in postnatal tissues and up-regulation in malignancies is driven by transcription factor E2f3 |
| Q40579171 | Experimental embryological analysis of genetic imprinting in mouse development |
| Q33850252 | Expression levels of insulin-like growth factors 1 and 2 in head and neck squamous cell carcinoma |
| Q37865526 | From Waddington's epigenetic landscape to small noncoding RNA: some important milestones in the history of epigenetics research |
| Q50302961 | Genes for Prader Willi syndrome/Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression |
| Q40948391 | Genetic conflict and evolution of mammalian X-chromosome inactivation |
| Q34032271 | Genetic control of intra-uterine growth |
| Q52220346 | Genetic imprinting in the mouse: implications for gene regulation. |
| Q70457181 | Genetic mosaicism in normal tissues of Wilms' tumour patients |
| Q72539974 | Genetics of Wilms' tumor: a blend of aberrant development and genomic imprinting |
| Q72872602 | Genomic imprinting and gene activation in cancer |
| Q37715275 | Genomic imprinting in development, growth, behavior and stem cells |
| Q26828858 | Genomic imprinting in mammals |
| Q38298288 | Genomic imprinting of Mash2, a mouse gene required for trophoblast development |
| Q38172016 | Genomic imprinting--the struggle of the genders at the molecular level |
| Q37068291 | Genomic imprinting: developmental significance and molecular mechanism |
| Q35833288 | Genomic imprinting: mechanism and role in human pathology |
| Q51860651 | Genomic imprinting: the emergence of an epigenetic paradigm. |
| Q67841611 | Hereditary tumours of childhood: Messages for cancer in general |
| Q36043897 | High-frequency genetic reversion mediated by a DNA duplication: the mouse pink-eyed unstable mutation |
| Q36471719 | IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome |
| Q89595427 | Imprinted Maternally Expressed microRNAs Antagonize Paternally Driven Gene Programs in Neurons |
| Q42623438 | Imprinting detection by extending a regression-based QTL analysis method |
| Q41566242 | Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome |
| Q71614540 | Imprinting moves to the centre |
| Q36969422 | Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome |
| Q40894082 | Increased prenatal IGF2 expression due to the porcine intron3-G3072A mutation may be responsible for increased muscle mass |
| Q77803706 | Insights into development and genetics from mouse chimeras |
| Q64068201 | Insulin-like Growth Factor II: An Essential Adult Stem Cell Niche Constituent in Brain and Intestine |
| Q41759014 | Insulin-like growth factor 2 and overgrowth: molecular biology and clinical implications |
| Q41377136 | Insulin-like growth factor 2 modulates murine hematopoietic stem cell maintenance through upregulation of p57. |
| Q56550684 | Isodisomy in BWS chromosomes |
| Q24534306 | Isoform-specific imprinting of the human PEG1/MEST gene |
| Q34026917 | Mammalian genomic imprinting. |
| Q96230919 | Maternal H3K27me3-dependent autosomal and X chromosome imprinting |
| Q76401306 | Maternal uniparental disomy of chromosome 16 in a case of spontaneous abortion |
| Q74312289 | Mechanisms of genomic imprinting |
| Q67521534 | Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11 |
| Q36888462 | Mosaic analysis with double markers reveals cell-type-specific paternal growth dominance. |
| Q33675226 | Mosaic uniparental disomy in Beckwith-Wiedemann syndrome. |
| Q50539794 | Mother and father in surprise genetic agreement. |
| Q35675706 | Mouse chromosome 7. |
| Q30495383 | Mouse homologues of human hereditary disease. |
| Q28512786 | MyoD regulates p57kip2 expression by interacting with a distant cis-element and modifying a higher order chromatin structure |
| Q35688004 | Next-Generation Sequencing Techniques Reveal that Genomic Imprinting Is Absent in Day-Old Gallus gallus domesticus Brains. |
| Q33965893 | Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome |
| 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. |
| Q39018235 | Origin and evolution of the metazoan non-coding regulatory genome |
| Q42629445 | Overexpression of IGF2R and IGF1R mRNA in SCNT-produced goats survived to adulthood |
| Q49161161 | Parental methylation patterns of a transgenic locus in adult somatic tissues are imprinted during gametogenesis |
| Q52174393 | Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation. |
| Q34363043 | Parental-origin-specific epigenetic modification of the mouse H19 gene |
| Q81476952 | Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion |
| Q36967749 | Paternally expressed genes predominate in the placenta. |
| Q48071136 | Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization |
| Q37712366 | Perturbations to the IGF1 growth pathway and adult energy homeostasis following disruption of mouse chromosome 12 imprinting. |
| Q31158518 | Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2 |
| Q92068265 | Prenatal dexamethasone exposure exerts sex-specific effect on placental oxygen and nutrient transport ascribed to the differential expression of IGF2 |
| Q48569804 | Proliferation and differentiation of androgenetic cells in fetal mouse chimeras |
| Q77129209 | Promoter-specific insulin-like growth factor 2 gene imprinting in human fetal liver and hepatoblastoma |
| Q33760043 | Regulation of imprinted expression by macro non-coding RNAs |
| Q52545355 | Relaxation of imprinted genes in human cancer. |
| Q59088779 | Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour |
| Q35267816 | Roles for genomic imprinting and the zygotic genome in placental development. |
| Q70972323 | Sequence characterization of alleles Gpi1-Sa and Gpi1-Sb at the glucose phosphate isomerase structural locus |
| Q33596012 | Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5). |
| Q33594511 | Sex ratios of affected and transmitting members of multiple case families with neural tube defects |
| Q34460281 | Silencing of miR-370 in human cholangiocarcinoma by allelic loss and interleukin-6 induced maternal to paternal epigenotype switch |
| Q41844735 | Structural analysis of the human insulin-like growth factor-II P3 promoter |
| Q64929446 | Technical advances contribute to the study of genomic imprinting. |
| Q50875072 | The conflict theory of genomic imprinting: how much can be explained? |
| Q41625119 | The contribution of the mouse to advances in human genetics |
| Q57802475 | The discovery and importance of genomic imprinting |
| Q33968784 | The evolution of genomic imprinting. |
| Q28742697 | The evolution of mammalian genomic imprinting was accompanied by the acquisition of novel CpG islands |
| Q38779863 | The evolving landscape of imprinted genes in humans and mice: Conflict among alleles, genes, tissues, and kin. |
| Q33628787 | The importance of imprinting in the human placenta. |
| Q28512597 | The imprinted Phlda2 gene regulates extraembryonic energy stores |
| Q35223922 | The molecular and cellular biology of insulin-like growth factor II |
| Q73208039 | The mouse chromosome 7 distal imprinting domain maps to G-bands F4/F5 |
| Q36236002 | The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito. |
| Q30530871 | The new dysmorphology: application of insights from basic developmental biology to the understanding of human birth defects |
| Q37022907 | The prevalence of loss of imprinting of H19 and IGF2 at birth. |
| Q35295496 | The role of imprinted genes in fetal growth abnormalities |
| Q35934507 | The structural H19 gene is required for transgene imprinting |
| Q58134238 | The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster |
| Q91474110 | Thromboinflammatory changes in plasma proteome of pregnant women with PCOS detected by quantitative label-free proteomics |
| 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 |
| Q41066237 | Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. |
| Q33389173 | Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain |
| 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 |
| Q93189824 | Understanding Cancer Through the Lens of Epigenetic Inheritance, Allele-Specific Gene Expression, and High-Throughput Technology |
| Q80558791 | [Colorectal carcinogenesis. 2. Underlying epigenetic and genetic alterations and molecular classification of colorectal cancers] |
| Q73563096 | [Parental genomic imprinting and its implications in growth] |
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