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/6JCategoriesSequencesSourceUniProtKB 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]CategoriesSequencesSourceUniProtKB 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/6JCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol 9:e1001091-e1001091 (2011)Cited in99+
SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways.Park J., Chen Y., Tishkoff D.X., Peng C., Tan M., Dai L., Xie Z., Zhang Y., Zwaans B.M.[...], Zhao Y.View abstractCited forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCMol. Cell 50:919-930 (2013)Cited in99+99+Mapped to6
No title available.EnsemblCited forIDENTIFICATIONStrainC57BL/6JSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to UniProtKB (JUN-2024)Cited in99+
Mtu1-Mediated Thiouridine Formation of Mitochondrial tRNAs Is Required for Mitochondrial Translation and Is Involved in Reversible Infantile Liver Injury.Wu Y., Wei F.Y., Kawarada L., Suzuki T., Araki K., Komohara Y., Fujimura A., Kaitsuka T., Takeya M.[...], Tomizawa K.View abstractCategoriesFunctionSourceMGI: 1347023PubMedEurope PMCPLoS Genet 12:e1006355-e1006355 (2016)Mapped to99+
Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome.Karpinski B.A., Maynard T.M., Fralish M.S., Nuwayhid S., Zohn I.E., Moody S.A., LaMantia A.S.View abstractCategoriesSequencesSourceMGI: 1347023PubMedEurope PMCDis Model Mech 7:245-257 (2014)Mapped to99+
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.Maynard T.M., Gopalakrishna D., Meechan D.W., Paronett E.M., Newbern J.M., LaMantia A.S.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 1347023PubMedEurope PMCHum Mol Genet 22:300-312 (2013)Mapped to99+
A high-resolution anatomical atlas of the transcriptome in the mouse embryo.Diez-Roux G., Banfi S., Sultan M., Geffers L., Anand S., Rozado D., Magen A., Canidio E., Pagani M.[...], Ballabio A.View abstractCategoriesExpressionSourceMGI: 1347023PubMedEurope PMCPLoS Biol 9:e1000582-e1000582 (2011)Mapped to99+
Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes.Maynard T.M., Meechan D.W., Dudevoir M.L., Gopalakrishna D., Peters A.Z., Heindel C.C., Sugimoto T.J., Wu Y., Lieberman J.A., Lamantia A.S.View abstractCategoriesSequencesSourceMGI: 1347023PubMedEurope PMCMol. Cell. Neurosci. 39:439-451 (2008)Cited in4Mapped to62
Effects of thioredoxin reductase-1 deletion on embryogenesis and transcriptome.Bondareva A.A., Capecchi M.R., Iverson S.V., Li Y., Lopez N.I., Lucas O., Merrill G.F., Prigge J.R., Siders A.M.[...], Schmidt E.E.View abstractCategoriesFunction, ExpressionSourceMGI: 1347023PubMedEurope PMCFree Radic Biol Med 43:911-923 (2007)Mapped to99+
BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system.Magdaleno S., Jensen P., Brumwell C.L., Seal A., Lehman K., Asbury A., Cheung T., Cornelius T., Batten D.M.[...], Curran T.CategoriesSequencesSourceMGI: 1347023PubMedEurope PMCPLoS Biol 4:e86-e86 (2006)Mapped to99+
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.Ivins S., Lammerts van Beuren K., Roberts C., James C., Lindsay E., Baldini A., Ataliotis P., Scambler P.J.View abstractCategoriesExpressionSourceMGI: 1347023PubMedEurope PMCDev Biol 285:554-569 (2005)Mapped to96
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.Prescott K., Ivins S., Hubank M., Lindsay E., Baldini A., Scambler P.View abstractCategoriesSequencesSourceMGI: 1347023PubMedEurope PMCHum Genet 116:486-496 (2005)Mapped to99+
GenePaint.org: an atlas of gene expression patterns in the mouse embryo.Visel A., Thaller C., Eichele G.View abstractCategoriesSequencesSourceMGI: 1347023PubMedEurope PMCNucleic Acids Res. 32:D552-D556 (2004)Cited in1Mapped to99+
A comprehensive analysis of 22q11 gene expression in the developing and adult brain.Maynard T.M., Haskell G.T., Peters A.Z., Sikich L., Lieberman J.A., LaMantia A.S.View abstractCategoriesSequences, ExpressionSourceMGI: 1347023PubMedEurope PMCProc Natl Acad Sci U S A 100:14433-14438 (2003)Mapped to99+
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 abstractCategoriesPhenotypes & VariantsSourceMGI: 1347023PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 100:14109-14114 (2003)Cited in1Mapped 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 abstractCategoriesSequencesSourceMGI: 1347023PubMedEurope PMCNature 420:563-573 (2002)Cited in699+Mapped to99+
Protein-protein interaction panel using mouse full-length cDNAs.Suzuki H., Fukunishi Y., Kagawa I., Saito R., Oda H., Endo T., Kondo S., Bono H., Okazaki Y., Hayashizaki Y.View abstractCategoriesFunction, InteractionSourceMGI: 1347023PubMedEurope PMCGenome Res 11:1758-1765 (2001)Mapped to99+
Functional annotation of a full-length mouse cDNA collection.Kawai J., Shinagawa A., Shibata K., Yoshino M., Itoh M., Ishii Y., Arakawa T., Hara A., Fukunishi Y.[...], Hayashizaki Y.View abstractCategoriesSequencesSourceMGI: 1347023PubMedEurope PMCNature 409:685-690 (2001)Cited in399+Mapped to99+
Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region.Puech A., Saint-Jore B., Merscher S., Russell R.G., Cherif D., Sirotkin H., Xu H., Factor S., Kucherlapati R., Skoultchi A.I.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 1347023PubMedEurope PMCProc Natl Acad Sci U S A 97:10090-10095 (2000)Mapped to99+
Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.Lund J., Chen F., Hua A., Roe B., Budarf M., Emanuel B.S., Reeves R.H.View abstractCategoriesSequencesSourceMGI: 1347023PubMedEurope PMCGenomics 63:374-383 (2000)Mapped to99+
Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.Lund J., Roe B., Chen F., Budarf M., Galili N., Riblet R., Miller R.D., Emanuel B.S., Reeves R.H.View abstractCategoriesSequencesSourceMGI: 1347023PubMedEurope PMCMamm Genome 10:438-443 (1999)Mapped to99+