The murine H19 gene is activated during embryonic stem cell differentiation in vitro and at the time of implantation in the developing embryo.Poirier F., Chan C.T., Timmons P.M., Robertson E.J., Evans M.J., Rigby P.W.View abstractCited forNUCLEOTIDE SEQUENCEStrainC57B1/6CategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCDevelopment 113:1105-1114 (1991)Cited in2Mapped to2
The sins of the fathers and mothers: genomic imprinting in mammalian development.Tilghman S.M.CategoriesFunction, SequencesSourceMGI: 95891PubMedEurope PMCCell 96:185-193 (1999)Mapped to35
The imprinted domain in mouse distal Chromosome 7: reagents for mutagenesis and sequencing.Day C.D., Smilinich N.J., Fitzpatrick G.V., deJong P.J., Shows T.B., Higgins M.J.CategoriesSequencesSourceMGI: 95891PubMedEurope PMCMamm Genome 10:182-185 (1999)Mapped to59
Cytosine methylation and mammalian development.Walsh C.P., Bestor T.H.View abstractCategoriesExpressionSourceMGI: 95891PubMedEurope PMCGenes Dev 13:26-34 (1999)Mapped to27
Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmel syndrome.Pellegrini M., Pilia G., Pantano S., Lucchini F., Uda M., Fumi M., Cao A., Schlessinger D., Forabosco A.View abstractCategoriesSequences, ExpressionSourceMGI: 95891PubMedEurope PMCDev Dyn 213:431-439 (1998)Mapped to22
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.Thorvaldsen J.L., Duran K.L., Bartolomei M.S.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 95891PubMedEurope PMCGenes Dev 12:3693-3702 (1998)Mapped to7
Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4.Nichols J., Zevnik B., Anastassiadis K., Niwa H., Klewe-Nebenius D., Chambers I., Scholer H., Smith A.View abstractCategoriesFunctionSourceMGI: 95891PubMedEurope PMCCell 95:379-391 (1998)Mapped to17
Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under- representation on the X chromosome.Ko M.S., Threat T.A., Wang X., Horton J.H., Cui Y., Wang X., Pryor E., Paris J., Wells-Smith J.[...], Nakashima H.View abstractCategoriesSequencesSourceMGI: 95891PubMedEurope PMCHum Mol Genet 7:1967-1978 (1998)Mapped to99+
Imprinted expression and methylation of the mouse H19 gene are conserved in extraembryonic lineages.Davis T.L., Tremblay K.D., Bartolomei M.S.View abstractCategoriesSequences, ExpressionSourceMGI: 95891PubMedEurope PMCDev Genet 23:111-118 (1998)Mapped to3
H19 and Igf2 are expressed and differentially imprinted in neuroectoderm- derived cells in the mouse brain.Hemberger M., Redies C., Krause R., Oswald J., Walter J., Fundele R.H.View abstractCategoriesSequences, ExpressionSourceMGI: 95891PubMedEurope PMCDev Genes Evol 208:393-402 (1998)Mapped to7
Sequence of a 42-kb mouse region containing the imprinted H19 locus: identification of a novel muscle-specific transcription unit showing biallelic expression.Ishihara K., Kato R., Furuumi H., Zubair M., Sasaki H.CategoriesSequencesSourceMGI: 95891PubMedEurope PMCMamm Genome 9:775-777 (1998)Mapped to5
Failure of egg cylinder elongation and mesoderm induction in mouse embryos lacking the tumor suppressor smad2.Weinstein M., Yang X., Li C., Xu X., Gotay J., Deng C.X.View abstractCategoriesFunctionSourceMGI: 95891PubMedEurope PMCProc Natl Acad Sci U S A 95:9378-9383 (1998)Mapped to27
Igf2 imprinting does not require its own DNA methylation or H19 RNA.Jones B.K., Levorse J.M., Tilghman S.M.View abstractCategoriesFunctionSourceMGI: 95891PubMedEurope PMCGenes Dev 12:2200-2207 (1998)Mapped to16
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.Paulsen M., Davies K.R., Bowden L.M., Villar A.J., Franck O., Fuermann M., Dean W.L., Moore T.F., Rodrigues N.[...], Walter J.View abstractCategoriesSequencesSourceMGI: 95891PubMedEurope PMCHum. Mol. Genet. 7:1149-1159 (1998)Cited in2Mapped to53
Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.Caspary T., Cleary M.A., Baker C.C., Guan X.J., Tilghman S.M.View abstractCategoriesSequences, ExpressionSourceMGI: 95891PubMedEurope PMCMol Cell Biol 18:3466-3474 (1998)Mapped to42
Altered imprinted gene methylation and expression in completely ES cell- derived mouse fetuses: association with aberrant phenotypes.Dean W., Bowden L., Aitchison A., Klose J., Moore T., Meneses J.J., Reik W., Feil R.View abstractCategoriesSequencesSourceMGI: 95891PubMedEurope PMCDevelopment 125:2273-2282 (1998)Mapped to19
Sequence-specific methylation of the mouse H19 gene in embryonic cells deficient in the Dnmt-1 gene.Warnecke P.M., Biniszkiewicz D., Jaenisch R., Frommer M., Clark S.J.View abstractCategoriesSequencesSourceMGI: 95891PubMedEurope PMCDev Genet 22:111-121 (1998)Mapped to2
Enhancer-dependent, locus-wide regulation of the imprinted mouse insulin- like growth factor II gene.Hatano N., Eversole-Cire P., Ferguson-Smith A.C., Jones P.A., Surani M.A., Sasaki H.View abstractCategoriesExpressionSourceMGI: 95891PubMedEurope PMCJ Biochem 123:984-991 (1998)Mapped to7
The tumor suppressor SMAD4/DPC4 is essential for epiblast proliferation and mesoderm induction in mice.Yang X., Li C., Xu X., Deng C.View abstractCategoriesFunctionSourceMGI: 95891PubMedEurope PMCProc Natl Acad Sci U S A 95:3667-3672 (1998)Mapped to25
Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis.Obata Y., Kaneko-Ishino T., Koide T., Takai Y., Ueda T., Domeki I., Shiroishi T., Ishino F., Kono T.View abstractCategoriesSequences, ExpressionSourceMGI: 95891PubMedEurope PMCDevelopment 125:1553-1560 (1998)Mapped to25
Location of enhancers is essential for the imprinting of H19 and Igf2 genes.Webber A.L., Ingram R.S., Levorse J.M., Tilghman S.M.View abstractCategoriesExpressionSourceMGI: 95891PubMedEurope PMCNature 391:711-715 (1998)Mapped to7
Imprinting of mouse Kvlqt1 is developmentally regulated.Gould T.D., Pfeifer K.View abstractCategoriesSequencesSourceMGI: 95891PubMedEurope PMCHum Mol Genet 7:483-487 (1998)Mapped to32
Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene.Miyoshi N., Kuroiwa Y., Kohda T., Shitara H., Yonekawa H., Kawabe T., Hasegawa H., Barton S.C., Surani M.A.[...], Ishino F.View abstractCategoriesSequencesSourceMGI: 95891PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 95:1102-1107 (1998)Cited in1Mapped to13
The paternal allele of the H19 gene is progressively silenced during early mouse development: the acetylation status of histones may be involved in the generation of variegated expression patterns.Svensson K., Mattsson R., James T.C., Wentzel P., Pilartz M., MacLaughlin J., Miller S.J., Olsson T., Eriksson U.J., Ohlsson R.View abstractCategoriesSequencesSourceMGI: 95891PubMedEurope PMCDevelopment 125:61-69 (1998)Mapped to2
Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes.Eggenschwiler J., Ludwig T., Fisher P., Leighton P.A., Tilghman S.M., Efstratiadis A.View abstractCategoriesSequencesSourceMGI: 95891PubMedEurope PMCGenes Dev 11:3128-3142 (1997)Mapped to16