| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Haruhiko Koseki | Q30502494 |
| P2093 | author name string | Yoichi Shinkai | |
| Jafar Sharif | |||
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| Human endogenous retroviruses: transposable elements with potential? | Q22065700 | ||
| The thrifty phenotype: An adaptation in growth or metabolism? | Q22252955 | ||
| New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish | Q24316006 | ||
| The origin and behavior of mutable loci in maize | Q24519263 | ||
| Human endogenous retroviruses in health and disease: a symbiotic perspective | Q24522289 | ||
| Evolution of the mammalian placenta revealed by phylogenetic analysis | Q24541507 | ||
| Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development | Q24681489 | ||
| The neighbor-joining method: a new method for reconstructing phylogenetic trees | Q25939010 | ||
| Positional cloning of zinc finger domain transcription factor Zfp69, a candidate gene for obesity-associated diabetes contributed by mouse locus Nidd/SJL | Q27312155 | ||
| Epigenetic reprogramming in mammalian development | Q28212171 | ||
| The Opitz syndrome gene Mid1 is transcribed from a human endogenous retroviral promoter | Q28212747 | ||
| Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder | Q28254567 | ||
| Meiotic and epigenetic aberrations in Dnmt3L-deficient male germ cells | Q28276068 | ||
| Association of the dihydrolipoamide dehydrogenase gene with Alzheimer's disease in an Ashkenazi Jewish population | Q28284062 | ||
| MITOPLD is a mitochondrial protein essential for nuage formation and piRNA biogenesis in the mouse germline | Q28510728 | ||
| DNA methylation of retrotransposon genes is regulated by Piwi family members MILI and MIWI2 in murine fetal testes | Q28513286 | ||
| Transgenerational inheritance of epigenetic states at the murine Axin(Fu) allele occurs after maternal and paternal transmission | Q28588249 | ||
| The SRA protein Np95 mediates epigenetic inheritance by recruiting Dnmt1 to methylated DNA | Q28589108 | ||
| Murine endogenous retroviruses | Q28602246 | ||
| What does CNTNAP2 reveal about autism spectrum disorder? | Q28708820 | ||
| A unified classification system for eukaryotic transposable elements | Q29617222 | ||
| Epigenetic inheritance at the agouti locus in the mouse | Q29617318 | ||
| Biology of mammalian L1 retrotransposons | Q29618630 | ||
| Transcription of IAP endogenous retroviruses is constrained by cytosine methylation | Q29618745 | ||
| Maternal dietary choline deficiency alters angiogenesis in fetal mouse hippocampus | Q30495988 | ||
| Genome-wide assessments reveal extremely high levels of polymorphism of two active families of mouse endogenous retroviral elements | Q33331558 | ||
| Global mapping of DNA methylation in mouse promoters reveals epigenetic reprogramming of pluripotency genes | Q33347134 | ||
| Identification of a novel murine IAP-promoted placenta-expressed gene | Q33391286 | ||
| LRP1 receptor controls adipogenesis and is up-regulated in human and mouse obese adipose tissue. | Q33510159 | ||
| The agouti mouse model: an epigenetic biosensor for nutritional and environmental alterations on the fetal epigenome | Q33658173 | ||
| Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function | Q33691446 | ||
| The characterisation of piRNA-related 19mers in the mouse | Q33932330 | ||
| Placenta-specific INSL4 expression is mediated by a human endogenous retrovirus element. | Q34179922 | ||
| Nonmotor Symptoms in Patients with PARK2 Mutations | Q34521178 | ||
| Maternal methyl supplements increase offspring DNA methylation at Axin Fused | Q34551157 | ||
| Epigenomic plasticity within populations: its evolutionary significance and potential. | Q34618183 | ||
| Knockdown of mental disorder susceptibility genes disrupts neuronal network physiology in vitro | Q35017276 | ||
| Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function | Q35144257 | ||
| Functional analysis of the endogenous retroviral promoter of the human endothelin B receptor gene | Q35149384 | ||
| Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome | Q35168999 | ||
| Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autism | Q35549465 | ||
| A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene. | Q35603666 | ||
| Germ-line epigenetic modification of the murine A vy allele by nutritional supplementation | Q35720918 | ||
| Ancestral capture of syncytin-Car1, a fusogenic endogenous retroviral envelope gene involved in placentation and conserved in Carnivora | Q35787321 | ||
| Resequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility | Q35898713 | ||
| Genetic mapping of habitual substance use, obesity-related traits, responses to mental and physical stress, and heart rate and blood pressure measurements reveals shared genes that are overrepresented in the neural synapse | Q36011131 | ||
| In vitro methylation inhibits the promotor activity of a cloned intracisternal A-particle LTR | Q36100071 | ||
| Development of structures and transport functions in the mouse placenta | Q36124326 | ||
| Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study | Q36406509 | ||
| Germ line-specific expression of intracisternal A-particle retrotransposons in transgenic mice | Q36561660 | ||
| Genomic evolution of the placenta using co-option and duplication and divergence | Q36586620 | ||
| Human trophoblast and choriocarcinoma expression of the growth factor pleiotrophin attributable to germ-line insertion of an endogenous retrovirus | Q37051625 | ||
| The evolution, regulation, and function of placenta-specific genes | Q37212214 | ||
| Keeping active endogenous retroviral-like elements in check: the epigenetic perspective | Q37279907 | ||
| HoxA-11 and FOXO1A cooperate to regulate decidual prolactin expression: towards inferring the core transcriptional regulators of decidual genes | Q37316627 | ||
| Genetic-epigenetic intersection in trophoblast differentiation: implications for extraembryonic tissue function | Q37677452 | ||
| Sirtuins mediate mammalian metabolic responses to nutrient availability | Q37976307 | ||
| Convergent evolution of endometrial prolactin expression in primates, mice, and elephants through the independent recruitment of transposable elements. | Q38698156 | ||
| The intracisternal A-particle gene family: structure and functional aspects | Q39608731 | ||
| Proviral silencing in embryonic stem cells requires the histone methyltransferase ESET. | Q39737989 | ||
| Intracisternal A particle genes: Distribution in the mouse genome, active subtypes, and potential roles as species-specific mediators of susceptibility to cancer | Q39760871 | ||
| Detection of IAP related transcripts in normal and transformed rat cells. | Q41733699 | ||
| The ORF1 protein encoded by LINE-1: structure and function during L1 retrotransposition | Q42373463 | ||
| KAP1 controls endogenous retroviruses in embryonic stem cells | Q43193929 | ||
| DNA methylation in ES cells requires the lysine methyltransferase G9a but not its catalytic activity | Q43251760 | ||
| Skeletal muscle expression of bone morphogenetic protein-1 and tolloid-like-1 extracellular proteases in different fiber types and in response to unloading, food deprivation and differentiation. | Q45906026 | ||
| Attenuation of diet-induced weight gain and adiposity through increased energy expenditure in mice lacking angiotensin II type 1a receptor | Q46477287 | ||
| Maternal epigenetics and methyl supplements affect agouti gene expression in Avy/a mice | Q47675900 | ||
| Identification of autonomous IAP LTR retrotransposons mobile in mammalian cells | Q47703333 | ||
| NINJ2 polymorphism is associated with ischemic stroke in Chinese Han population | Q49100954 | ||
| Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD). | Q50312325 | ||
| Lipid metabolic effect of Korean red ginseng extract in mice fed on a high-fat diet | Q50526203 | ||
| Silencing of endogenous retroviruses: when and why do histone marks predominate? | Q51834987 | ||
| An abundant placental transcript containing an IAP-LTR is allelic to mouse pregnancy-specific glycoprotein 23 (Psg23): cloning and genetic analysis. | Q52958191 | ||
| A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease. | Q53237496 | ||
| Maternal protein restriction affects gene expression profiles in the kidney at weaning with implications for the regulation of renal function and lifespan. | Q54668956 | ||
| Activation of intracistemal a particles by 5-azacytidine in mouse Ki-BALB cell line | Q72710915 | ||
| The developmental origins of adult disease | Q80041697 | ||
| Gtsf1/Cue110, a gene encoding a protein with two copies of a CHHC Zn-finger motif, is involved in spermatogenesis and retrotransposon suppression in murine testes | Q84524065 | ||
| Divergence of CpG island promoters: a consequence or cause of evolution? | Q84581456 | ||
| Hypomethylation of functional retrotransposon-derived genes in the human placenta | Q84847757 | ||
| P433 | issue | 1609 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 20110340 | |
| P577 | publication date | 2013-01-05 | |
| P1433 | published in | Philosophical Transactions of the Royal Society B | Q2153239 |
| P1476 | title | Is there a role for endogenous retroviruses to mediate long-term adaptive phenotypic response upon environmental inputs? | |
| P478 | volume | 368 |
| Q28542838 | DNA methylation is dispensable for suppression of the agouti viable yellow controlling element in murine embryonic stem cells |
| Q91693298 | Endogenous Retroviruses Activity as a Molecular Signature of Neurodevelopmental Disorders |
| Q47556317 | High expression of Endogenous Retroviruses from intrauterine life to adulthood in two mouse models of Autism Spectrum Disorders |
| Q34084264 | Longitudinal epigenetic drift in mice perinatally exposed to lead. |
| Q42562542 | Mammalian epigenetics in biology and medicine |
| Q99591065 | Neonatal Lead (Pb) Exposure and DNA Methylation Profiles in Dried Bloodspots |
| Q37414998 | Obesity-induced sperm DNA methylation changes at satellite repeats are reprogrammed in rat offspring. |
| Q38612083 | Perinatal lead (Pb) exposure results in sex and tissue-dependent adult DNA methylation alterations in murine IAP transposons. |
| Q50025249 | The effects of nutrient restriction on mRNA expression of endogenous retroviruses, interferon-tau, and pregnancy specific protein-B during the establishment of pregnancy in beef heifers |
| Q34456484 | Transpositional shuffling and quality control in male germ cells to enhance evolution of complex organisms |
| Q97870674 | Viruses in the reproductive tract: On their way to the germ line? |
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