Lineage-specific biology revealed by a finished genome assembly of the mouse.Church D.M., Goodstadt L., Hillier L.W., Zody M.C., Goldstein S., She X., Bult C.J., Agarwala R., Cherry J.L.[...], Ponting C.P.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]StrainC57BL/6JCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
A tissue-specific atlas of mouse protein phosphorylation and expression.Huttlin E.L., Jedrychowski M.P., Elias J.E., Goswami T., Rad R., Beausoleil S.A., Villen J., Haas W., Sowa M.E., Gygi S.P.View abstractCited forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCCell 143:1174-1189 (2010)Cited in99+99+Mapped to6
Modernizing reference genome assemblies.Church D.M., Schneider V.A., Graves T., Auger K., Cunningham F., Bouk N., Chen H.C., Agarwala R., McLaren W.M.[...], Hubbard T.Cited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]StrainC57BL/6JCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol 9:e1001091-e1001091 (2011)Cited in99+
No title available.EnsemblCited forIDENTIFICATIONStrainC57BL/6JSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to UniProtKB (AUG-2024)Cited in99+
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.CategorySequencesSourceMGI: 1861712PubMedEurope PMCMamm Genome 10:182-185 (1999)Mapped to59
Transcription factor ASCL2 is required for development of the glycogen trophoblast cell lineage.Bogutz A.B., Oh-McGinnis R., Jacob K.J., Ho-Lau R., Gu T., Gertsenstein M., Nagy A., Lefebvre L.View abstractCategoryExpressionSourceMGI: 1861712PubMedEurope PMCPLoS Genet 14:e1007587-e1007587 (2018)Mapped to33
Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction.Oh-McGinnis R., Bogutz A.B., Lefebvre L.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1861712PubMedEurope PMCDev Biol 351:277-286 (2011)Mapped to42
Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1.Mohammad F., Mondal T., Guseva N., Pandey G.K., Kanduri C.View abstractCategoriesFunction, ExpressionSourceMGI: 1861712PubMedEurope PMCDevelopment 137:2493-2499 (2010)Mapped to69
Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.Oh-McGinnis R., Bogutz A.B., Lee K.Y., Higgins M.J., Lefebvre L.View abstractCategorySequencesSourceMGI: 1861712PubMedEurope PMCBMC Dev Biol 10:50-50 (2010)Mapped to47
A murine even-skipped homologue, Evx 1, is expressed during early embryogenesis and neurogenesis in a biphasic manner.Bastian H., Gruss P.View abstractCategorySequencesSourceMGI: 1861712PubMedEurope PMCEMBO J. 9:1839-1852 (1990)Cited in1Mapped to48
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.Hansen G.M., Markesich D.C., Burnett M.B., Zhu Q., Dionne K.M., Richter L.J., Finnell R.H., Sands A.T., Zambrowicz B.P., Abuin A.View abstractCategorySequencesSourceMGI: 1861712PubMedEurope PMCGenome Res 18:1670-1679 (2008)Mapped to99+
Two distinct mechanisms of silencing by the KvDMR1 imprinting control region.Shin J.Y., Fitzpatrick G.V., Higgins M.J.View abstractCategoryExpressionSourceMGI: 1861712PubMedEurope PMCEMBO J 27:168-178 (2008)Mapped to43
A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA.Green K., Lewis A., Dawson C., Dean W., Reinhart B., Chaillet J.R., Reik W.View abstractCategoryExpressionSourceMGI: 1861712PubMedEurope PMCMamm Genome 18:32-42 (2007)Mapped to39
Epigenetic dynamics of the Kcnq1 imprinted domain in the early embryo.Lewis A., Green K., Dawson C., Redrup L., Huynh K.D., Lee J.T., Hemberger M., Reik W.View abstractCategoriesSequences, ExpressionSourceMGI: 1861712PubMedEurope PMCDevelopment 133:4203-4210 (2006)Mapped to33
Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes.Mancini-Dinardo D., Steele S.J., Levorse J.M., Ingram R.S., Tilghman S.M.View abstractCategoriesFunction, ExpressionSourceMGI: 1861712PubMedEurope PMCGenes Dev 20:1268-1282 (2006)Mapped to34
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.Cerrato F., Sparago A., Di Matteo I., Zou X., Dean W., Sasaki H., Smith P., Genesio R., Bruggemann M.[...], Riccio A.View abstractCategoryFunctionSourceMGI: 1861712PubMedEurope PMCHum Mol Genet 14:503-511 (2005)Mapped to31
Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.Umlauf D., Goto Y., Cao R., Cerqueira F., Wagschal A., Zhang Y., Feil R.View abstractCategoryFunctionSourceMGI: 1861712PubMedEurope PMCNat. Genet. 36:1296-1300 (2004)Cited in3Mapped to48
Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.Lewis A., Mitsuya K., Umlauf D., Smith P., Dean W., Walter J., Higgins M., Feil R., Reik W.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 1861712PubMedEurope PMCNat Genet 36:1291-1295 (2004)Mapped to45
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.Zambrowicz B.P., Abuin A., Ramirez-Solis R., Richter L.J., Piggott J., BeltrandelRio H., Buxton E.C., Edwards J., Finch R.A.[...], Sands A.T.View abstractCategoryPhenotypes & VariantsSourceMGI: 1861712PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 100:14109-14114 (2003)Cited in1Mapped to99+
Gene density and transcription influence the localization of chromatin outside of chromosome territories detectable by FISH.Mahy N.L., Perry P.E., Bickmore W.A.View abstractCategoriesSequences, ExpressionSourceMGI: 1861712PubMedEurope PMCJ Cell Biol 159:753-763 (2002)Mapped to99+
Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R.[...], Hayashizaki Y.View abstractCategorySequencesSourceMGI: 1861712PubMedEurope PMCNature 420:563-573 (2002)Cited in699+Mapped to99+
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1.Fitzpatrick G.V., Soloway P.D., Higgins M.J.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 1861712PubMedEurope PMCNat Genet 32:426-431 (2002)Mapped to77
Microarray expression profiling of tissues from mice with uniparental duplications of chromosomes 7 and 11 to identify imprinted genes.Choi J.D., Underkoffler L.A., Collins J.N., Marchegiani S.M., Terry N.A., Beechey C.V., Oakey R.J.View abstractCategoryExpressionSourceMGI: 1861712PubMedEurope PMCMamm Genome 12:758-764 (2001)Mapped to99
Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain.Onyango P., Miller W., Lehoczky J., Leung C.T., Birren B., Wheelan S., Dewar K., Feinberg A.P.View abstractCategorySequencesSourceMGI: 1861712PubMedEurope PMCGenome Res 10:1697-1710 (2000)Mapped to87
Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.Engemann S., Stroedicke M., Paulsen M., Franck O., Reinhardt R., Lane N., Reik W., Walter J.View abstractCategorySequencesSourceMGI: 1861712PubMedEurope PMCHum. Mol. Genet. 9:2691-2706 (2000)Cited in73Mapped to91