| scholarly article | Q13442814 |
| P2093 | author name string | Keverne EB | |
| Surani MA | |||
| Ishino F | |||
| Lefebvre L | |||
| Barton SC | |||
| Viville S | |||
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| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 163-169 | |
| P577 | publication date | 1998-10-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest | |
| P478 | volume | 20 |
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| Q52121639 | A possible role for imprinted genes in inbreeding avoidance and dispersal from the natal area in mice. |
| Q36169619 | A set of imprinted genes required for normal body growth also promotes growth of rhabdomyosarcoma cells |
| Q50645854 | Aberrant DNA methylation of imprinted loci in superovulated oocytes. |
| Q40085760 | Activation of paternally expressed imprinted genes in newly derived germline-competent mouse parthenogenetic embryonic stem cell lines |
| Q48379561 | Age-related trends in gene expression in the chemosensory-nasal mucosae of senescence-accelerated mice |
| Q28510453 | Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities |
| Q50424549 | Alteration in methylation level at differential methylated regions of MEST and DLK1 in fetus of preeclampsia |
| 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. |
| Q37136956 | An extensive genetic program occurring during postnatal growth in multiple tissues |
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| Q34743767 | Annotation: The 'effects' of parenting reconsidered: findings, challenges, and applications |
| Q35754088 | Assisted reproduction causes placental maldevelopment and dysfunction linked to reduced fetal weight in mice. |
| Q34083377 | Association of maternally inherited GNAS alleles with African-American male birth weight |
| Q35469233 | Association of telomere length with authentic pluripotency of ES/iPS cells |
| Q36994734 | Associations between antibiotic exposure during pregnancy, birth weight and aberrant methylation at imprinted genes among offspring |
| Q33405733 | At least ten genes define the imprinted Dlk1-Dio3 cluster on mouse chromosome 12qF1 |
| Q38089794 | Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth |
| Q35109913 | Behavior genetics |
| Q34187521 | Behavioral epigenetics |
| Q88768131 | Beyond the maternal epigenetic legacy |
| Q34393357 | Brain preparations for maternity--adaptive changes in behavioral and neuroendocrine systems during pregnancy and lactation. An overview |
| Q38131371 | Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10. |
| Q39411453 | Candidate DNA methylation drivers of acquired cisplatin resistance in ovarian cancer identified by methylome and expression profiling |
| Q49832279 | Catalytic activities of mammalian epoxide hydrolases with cis and trans fatty acid epoxides relevant to skin barrier function |
| Q33285306 | Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. |
| Q36173051 | Cell Pluripotency Levels Associated with Imprinted Genes in Human |
| Q89877199 | Cellular Heterogeneity and Lineage Restriction during Mouse Digit Tip Regeneration at Single-Cell Resolution |
| Q34505224 | Cellular functions of genetically imprinted genes in human and mouse as annotated in the gene ontology |
| Q35087750 | Changes in maternal gene expression in olfactory circuits in the immediate postpartum period |
| Q57828942 | Childbirth in prehistory: An introduction |
| Q28584750 | Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development |
| Q27006276 | Coadaptation and conflict, misconception and muddle, in the evolution of genomic imprinting |
| Q34043222 | Competing interactions between micro-RNAs determine neural progenitor survival and proliferation after ethanol exposure: evidence from an ex vivo model of the fetal cerebral cortical neuroepithelium |
| Q36436496 | Complementation hypothesis: the necessity of a monoallelic gene expression mechanism in mammalian development. |
| Q87419077 | Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylation |
| Q34305206 | Culture of oocytes and risk of imprinting defects. |
| Q36298136 | Current models and future directions for understanding the neural circuitries of maternal behaviors in rodents |
| Q30275297 | DNA Methylation of Regulatory Regions of Imprinted Genes at Birth and Its Relation to Infant Temperament |
| Q36383223 | DNA methylation in the human placenta and fetal growth (review). |
| Q47599271 | Deletion of the miR-379/miR-410 gene cluster at the imprinted Dlk1-Dio3 locus enhances anxiety-related behaviour |
| Q33825610 | Diet-induced adipose tissue expansion is mitigated in mice with a targeted inactivation of mesoderm specific transcript (Mest). |
| Q47701588 | Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation |
| Q36733095 | Different roles for Tet1 and Tet2 proteins in reprogramming-mediated erasure of imprints induced by EGC fusion |
| Q34342504 | Differentially methylated regions of imprinted genes in prenatal, perinatal and postnatal human tissues. |
| Q28941781 | Discovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4 |
| Q39432488 | Do social insects support Haig's kin theory for the evolution of genomic imprinting? |
| Q77892020 | Do we understand the evolution of genomic imprinting? |
| Q34994085 | Dynamic expression of imprinted genes associates with maternally controlled nutrient allocation during maize endosperm development. |
| Q36956223 | Effects of in vitro maturation on gene expression in rhesus monkey oocytes |
| Q47306576 | Effects of maternal folic acid supplementation on gene methylation and being small for gestational age. |
| Q33586272 | Effects of ooplasm manipulation on DNA methylation and growth of progeny in mice |
| Q28279818 | Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight |
| Q48656418 | Emotional reactivity in mice, a case of nongenetic heredity? |
| Q38626695 | Epigenesis and plasticity of mouse trophoblast stem cells |
| Q36421376 | Epigenetic and phenotypic consequences of a truncation disrupting the imprinted domain on distal mouse chromosome 7. |
| Q37961857 | Epigenetics and brain evolution |
| Q37801493 | Epigenetics and the placenta |
| Q36950149 | Epigenetics of gestational diabetes mellitus and offspring health: the time for action is in early stages of life |
| Q37148602 | Epigenetics, brain evolution and behaviour |
| Q41825130 | Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology |
| Q35661315 | Evidence That Up-Regulation of MicroRNA-29 Contributes to Postnatal Body Growth Deceleration |
| Q62632007 | Evolution and ageing |
| Q52114634 | Expression of Peg1 (Mest) in the developing mouse heart: involvement in trabeculation. |
| Q28145015 | Expression of the imprinted genes MEST/Mest in human and murine placenta suggests a role in angiogenesis |
| Q33425018 | Expression profile and transcription factor binding site exploration of imprinted genes in human and mouse |
| Q35909440 | Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profilingof the t(12;14) and evidence in support of predisposing genetic heterogeneity |
| Q46961163 | Female promiscuity and maternally dependent offspring growth rates in mammals. |
| Q28215251 | Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma |
| Q35463175 | G-quadruplex structures and CpG methylation cause drop-out of the maternal allele in polymerase chain reaction amplification of the imprinted MEST gene promoter |
| Q35563016 | GNAS Spectrum of Disorders |
| Q34958754 | Gatm, a creatine synthesis enzyme, is imprinted in mouse placenta |
| Q34215458 | Gene expression analysis in Interleukin-12-induced suppression of mouse mammary carcinoma |
| Q42833076 | Gene expression of mesoderm-specific transcript is upregulated as preadipocytes differentiate to adipocytes in vitro |
| Q33927893 | Gene interactions in the evolution of genomic imprinting. |
| Q36428167 | Generalized disruption of inherited genomic imprints leads to wide-ranging placental defects and dysregulated fetal growth |
| Q37961799 | Genetic and epigenetic dysregulation of imprinted genes in the brain |
| Q77883178 | Genetic conflicts and the private life of Peromyscus polionotus |
| Q34032271 | Genetic control of intra-uterine growth |
| Q34056811 | Genetically caused retarded growth in animals |
| Q28586104 | Genome-wide and parental allele-specific analysis of CTCF and cohesin DNA binding in mouse brain reveals a tissue-specific binding pattern and an association with imprinted differentially methylated regions |
| Q36436558 | Genome-wide survey of imprinted genes |
| Q43065698 | Genomic characterisation of a Fgf-regulated gradient-based neocortical protomap |
| Q35533142 | Genomic conflicts and sexual antagonism in human health: insights from oxytocin and testosterone |
| Q50301666 | Genomic imprinting and conflict-induced decanalization |
| Q91596236 | Genomic imprinting and its effects on postnatal growth and adult metabolism |
| Q37769333 | Genomic imprinting and mammalian reproduction. |
| Q36949014 | Genomic imprinting and the evolution of sex differences in mammalian reproductive strategies |
| Q34393452 | Genomic imprinting and the maternal brain |
| Q35575191 | Genomic imprinting and the social brain |
| Q37715275 | Genomic imprinting in development, growth, behavior and stem cells |
| Q21145256 | Genomic imprinting in mammals: emerging themes and established theories |
| Q48003531 | Genomic imprinting is disrupted in interspecific Peromyscus hybrids |
| Q85068250 | Genomic imprinting status of IGF-II and H19 in placentas of fetal growth restriction patients |
| Q33541538 | Genomic imprinting: implications for human disease |
| Q29616227 | Genomic imprinting: parental influence on the genome |
| Q34535703 | HP1BP3 expression determines maternal behavior and offspring survival |
| Q28507539 | Heterotrimeric G proteins of the Gq/11 family are crucial for the induction of maternal behavior in mice |
| Q48376672 | Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder |
| Q60358310 | Hyperstimulation of CaSR in human MSCs by biomimetic apatite inhibits endochondral ossification via temporal down-regulation of PTH1R |
| Q36205983 | Hypothalamic expression of Peg3 gene is associated with maternal care differences between SM/J and LG/J mouse strains |
| Q35817149 | Identification of Mest/Peg1 gene expression as a predictive biomarker of adipose tissue expansion sensitive to dietary anti-obesity interventions |
| Q33680910 | Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6. |
| Q52121623 | Identification of developmentally regulated mesodermal-specific transcript in mouse embryonic metanephros. |
| Q64116184 | Imatinib treatments have long-term impact on placentation and embryo survival |
| Q52089452 | Implications of cloning technique for reproductive medicine. |
| Q36515797 | Importance of the matriline for genomic imprinting, brain development and behaviour |
| Q33724476 | Imprinted Nesp55 influences behavioral reactivity to novel environments |
| Q26829945 | Imprinted Zac1 in neural stem cells |
| Q34093571 | Imprinted genes and mental dysfunction |
| Q37060646 | Imprinted genes and neuroendocrine function |
| Q36436584 | Imprinted genes and their role in human fetal growth. |
| Q33852775 | Imprinted genes as potential genetic and epigenetic toxicologic targets |
| Q90557455 | Imprinted genes influencing the quality of maternal care |
| Q51975646 | Imprinted genes, cognition and behaviour. |
| Q35043723 | Imprinting and disease |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q61804540 | Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability |
| Q33873823 | Improving the safety of embryo technologies: possible role of genomic imprinting |
| Q35226250 | In vitro lead exposure changes DNA methylation and expression of IGF2 and PEG1/MEST. |
| Q36247349 | Increased Histone Deacetylase Activity Involved in the Suppressed Invasion of Cancer Cells Survived from ALA-Mediated Photodynamic Treatment |
| Q48140497 | Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors |
| Q37710116 | Influence of maternal obesity, diet and exercise on epigenetic regulation of adipocytes |
| Q92982560 | Intragenomic conflict over bet-hedging |
| Q37909236 | Is there a genomically imprinted social brain? |
| Q24534306 | Isoform-specific imprinting of the human PEG1/MEST gene |
| Q78168570 | It's a knockout! |
| Q37033645 | Knockdown of CDKN1C (p57(kip2)) and PHLDA2 results in developmental changes in bovine pre-implantation embryos |
| Q47655979 | Loss-of-imprinting of Peg1 in mouse interspecies hybrids is correlated with altered growth |
| Q34325361 | Low frequency of imprinting defects in ICSI children born small for gestational age. |
| Q50350055 | Maintenance of Mest imprinted methylation in blastocyst-stage mouse embryos is less stable than other imprinted loci following superovulation or embryo culture. |
| Q22336963 | Male-mediated developmental toxicity |
| Q34026917 | Mammalian genomic imprinting. |
| Q36742624 | Maternal Diet during Pregnancy Induces Gene Expression and DNA Methylation Changes in Fetal Tissues in Sheep |
| Q34110258 | Maternal behavior and developmental psychopathology |
| Q51644618 | Maternal care affects the development of maternal behavior in inbred mice. |
| Q56889416 | Maternal care boosted by paternal imprinting in mammals |
| Q30475378 | Maternal genetic mutations as gestational and early life influences in producing psychiatric disease-like phenotypes in mice |
| Q35038158 | Maternal imprints and the origins of variation. |
| Q38692978 | Maternal inflammatory diet and adverse pregnancy outcomes: Circulating cytokines and genomic imprinting as potential regulators? |
| Q52668639 | Maternal modulation of paternal effects on offspring development. |
| Q41610496 | Maternal nutrition during pregnancy is associated with differential expression of imprinted genes and DNA methyltranfereases in muscle of beef cattle offspring |
| Q37367108 | Maternal prenatal depression is associated with decreased placental expression of the imprinted gene PEG3 |
| Q34607086 | Maternal stress, preterm birth, and DNA methylation at imprint regulatory sequences in humans |
| Q40135246 | Maternal vitamin D, DNA methylation at imprint regulatory regions and offspring weight at birth, 1 year and 3 years |
| Q36223114 | Mesoderm-specific transcript (MEST) is a negative regulator of human adipocyte differentiation |
| Q28506024 | Mesoderm-specific transcript is associated with fat mass expansion in response to a positive energy balance |
| Q35670415 | Mest but Not MiR-335 Affects Skeletal Muscle Growth and Regeneration |
| Q37583989 | Mest/Peg1 Is Essential for the Development and Maintenance of a SNc Neuronal Subset |
| Q42813752 | Mest/Peg1 inhibits Wnt signalling through regulation of LRP6 glycosylation |
| Q36720609 | Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitus. |
| Q41640900 | Methods of epigenome editing for probing the function of genomic imprinting |
| Q35922196 | Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta development |
| Q37479026 | Methylation Status of H19/IGF2 Differentially Methylated Region in in vitro Human Blastocysts Donated by Healthy Couples. |
| Q48594052 | Methylation and expression analyses of the 7q autism susceptibility locus genes MEST , COPG2, and TSGA14 in human and anthropoid primate cortices. |
| Q35963130 | MicroRNAs and Fetal Brain Development: Implications for Ethanol Teratology during the Second Trimester Period of Neurogenesis. |
| Q34078032 | MicroRNAs: master regulators of ethanol abuse and toxicity? |
| Q33492605 | Modeling genetic imprinting effects of DNA sequences with multilocus polymorphism data |
| Q36455952 | Modes of imprinted gene action in learning disability |
| Q34399056 | Molecular characterization of the Neuronatin gene in the porcine placenta |
| Q47851124 | Monoalleleic transcription of the insulin-like growth factor-II gene (Igf2) in chick embryos |
| Q34085483 | Monotreme IGF2 expression and ancestral origin of genomic imprinting |
| Q38315593 | Multilocus methylation defects in imprinting disorders. |
| Q28211002 | Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region |
| Q36555585 | Mutations in the TSGA14 gene in families with autism spectrum disorders |
| Q28586253 | Neonatal lethality, dwarfism, and abnormal brain development in Dmbx1 mutant mice |
| Q37288046 | Neural control of sexually dimorphic behaviors |
| Q57074714 | Neuronatin deletion causes postnatal growth restriction and adult obesity in 129S2/Sv mice |
| Q37445958 | New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain |
| Q33721781 | Newborns of obese parents have altered DNA methylation patterns at imprinted genes. |
| Q37437821 | Novel epigenetic mechanisms that control pluripotency and quiescence of adult bone marrow-derived Oct4(+) very small embryonic-like stem cells |
| Q50650528 | Oocyte growth-dependent progression of maternal imprinting in mice. |
| Q36436505 | Origins of extreme sexual dimorphism in genomic imprinting. |
| Q35258669 | Oxytocin and social motivation |
| Q34351507 | PEG1/MEST and IGF2 DNA methylation in CIN and in cervical cancer. |
| Q51324473 | Parental antagonism and parent-offspring co-adaptation interact to shape family life. |
| Q35737547 | Partial Loss of Genomic Imprinting Reveals Important Roles for Kcnq1 and Peg10 Imprinted Domains in Placental Development |
| Q34356609 | Paternal factors and schizophrenia risk: de novo mutations and imprinting |
| Q50854130 | Peromysci, promiscuity and imprinting. |
| Q46152291 | Pharmacologic inhibition of epigenetic modification reveals targets of aberrant promoter methylation in Ewing sarcoma |
| Q59030457 | Piece of cake |
| Q35217003 | Placental protection of the fetal brain during short-term food deprivation |
| Q34135795 | Placental-specific IGF-II is a major modulator of placental and fetal growth. |
| Q50763500 | Placentas from pregnancies conceived by IVF/ICSI have a reduced DNA methylation level at the H19 and MEST differentially methylated regions. |
| Q34240242 | Plagiarized bacterial genes in the human book of life |
| Q35038510 | Population models of genomic imprinting. II. Maternal and fertility selection |
| Q35881887 | Quantitative and functional interrogation of parent-of-origin allelic expression biases in the brain |
| Q37615337 | Quantitative expression of developmental genes, Pou5f1 (Oct4) and Mest (Peg1), in vitrified mouse embryos |
| Q47844861 | Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception. |
| Q35134305 | Reductions in expression of growth regulating genes in skeletal muscle with age in wild type and myostatin null mice |
| Q36436592 | Regulation of growth and metabolism by imprinted genes |
| Q35058363 | Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. |
| Q34033384 | Representing sex in the brain, one module at a time. |
| Q34426502 | Reprogramming of genome function through epigenetic inheritance |
| Q33575632 | Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome |
| Q24616417 | Rett syndrome and MeCP2: linking epigenetics and neuronal function |
| Q37317744 | Review paper: a review of the pathology of abnormal placentae of somatic cell nuclear transfer clone pregnancies in cattle, sheep, and mice. |
| Q34736493 | Role of epigenetics in mental disorders |
| Q35458473 | Roles of imprinted genes in neural stem cells |
| Q36411455 | Selected imprinting of INS in the marsupial |
| Q36268899 | Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST |
| Q34465575 | Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions |
| Q51014930 | Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b. |
| Q36436534 | Small non-coding RNAs and genomic imprinting |
| Q38060071 | Small regulatory RNAs controlled by genomic imprinting and their contribution to human disease |
| Q33985684 | Sociogenomics: social life in molecular terms |
| Q26852157 | The GNAS complex locus and human diseases associated with loss-of-function mutations or epimutations within this imprinted gene |
| Q37078658 | The Precise Structures and Stereochemistry of Trihydroxy-linoleates Esterified in Human and Porcine Epidermis and Their Significance in Skin Barrier Function: IMPLICATION OF AN EPOXIDE HYDROLASE IN THE TRANSFORMATIONS OF LINOLEATE. |
| Q34421524 | The developmental program of the hypothalamus and its disorders |
| Q36927144 | The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region |
| Q28742697 | The evolution of mammalian genomic imprinting was accompanied by the acquisition of novel CpG islands |
| Q34992967 | The genetics of the Silver-Russell syndrome |
| Q33843172 | The impact of genomic imprinting for neurobehavioral and developmental disorders |
| Q33628787 | The importance of imprinting in the human placenta. |
| Q51976832 | The imprinted gene Magel2 regulates normal circadian output. |
| Q24677893 | The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome |
| Q48484159 | The inheritance of cognitive skills: does genomic imprinting play a role? |
| Q39030336 | The neurobiology of parenting: A neural circuit perspective |
| Q28083223 | The role and interaction of imprinted genes in human fetal growth |
| Q34426232 | The role of genomic imprinting in biology and disease: an expanding view |
| Q35295496 | The role of imprinted genes in fetal growth abnormalities |
| Q34467097 | The role of tissue-specific imprinting as a source of phenotypic heterogeneity in human disease. |
| Q50532990 | The sins of the fathers and mothers: genomic imprinting in mammalian development. |
| Q28586677 | The winged helix gene, Foxb1, controls development of mammary glands and regions of the CNS that regulate the milk-ejection reflex |
| Q35780129 | Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2 |
| Q36629581 | Transient neonatal diabetes, ZFP57, and hypomethylation of multiple imprinted loci: a detailed follow-up |
| Q38351359 | Two ENU-induced mutations in Rasgrf1 and early mouse growth retardation. |
| Q36001933 | Unique patterns of evolutionary conservation of imprinted genes |
| Q34327064 | Variable imprinting of the MEST gene in human preimplantation embryos. |
| Q38246516 | What does genetics tell us about imprinting and the placenta connection? |
| Q33338342 | What good is genomic imprinting: the function of parent-specific gene expression |
| Q26853193 | Why we should transfer frozen instead of fresh embryos: the translational rationale |
| 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 |
| Q28137721 | gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome |
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