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+
No title available.EnsemblCited forIDENTIFICATIONStrainC57BL/6JSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to UniProtKB (JUN-2024)Cited in99+
Genomics and hearing impairment.Keats B.J., Berlin C.I.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCGenome Res 9:7-16 (1999)Mapped to35
Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells.Xiang M., Gao W.Q., Hasson T., Shin J.J.View abstractCategoriesExpressionSourceMGI: 104510PubMedEurope PMCDevelopment 125:3935-3946 (1998)Mapped to28
Mutation analysis of the mouse myosin VIIA deafness gene.Mburu P., Liu X.-Z., Walsh J., Saw D. Jr., Cope M.J., Gibson F., Kendrick-Jones J., Steel K.P., Brown S.D.M.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCGenes Funct. 1:191-203 (1997)Cited in1Mapped to7
Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice.Liu X., Ondek B., Williams D.S.CategoriesFunctionSourceMGI: 104510PubMedEurope PMCNat Genet 19:117-118 (1998)Mapped to8
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.Self T., Mahony M., Fleming J., Walsh J., Brown S.D., Steel K.P.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 104510PubMedEurope PMCDevelopment 125:557-566 (1998)Mapped to8
Unconventional myosins, the basis for deafness in mouse and man.Hasson T.CategoriesFunction, SequencesSourceMGI: 104510PubMedEurope PMCAm J Hum Genet 61:801-805 (1997)Mapped to8
Expression of myosin VIIA during mouse embryogenesis.Sahly I., El-Amraoui A., Abitbol M., Petit C., Dufier J.L.View abstractCategoriesSequences, ExpressionSourceMGI: 104510PubMedEurope PMCAnat Embryol (Berl) 196:159-170 (1997)Mapped to8
Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression.Hasson T., Walsh J., Cable J., Mooseker M.S., Brown S.D., Steel K.P.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCCell Motil Cytoskeleton 37:127-138 (1997)Mapped to8
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.Liu X.-Z., Walsh J., Mburu P., Kendrick-Jones J., Cope M.J., Steel K.P., Brown S.D.M.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCNat. Genet. 16:188-190 (1997)Cited in1Mapped to8
Shaker mice and a peek into the House of Usher.Saw D. Jr., Steel K.P., Brown S.D.CategoriesFunctionSourceMGI: 104510PubMedEurope PMCExp Anim 46:1-9 (1997)Mapped to8
Mapping of unconventional myosins in mouse and human.Hasson T., Skowron J.F., Gilbert D.J., Avraham K.B., Perry W.L., Bement W.M., Anderson B.L., Sherr E.H., Chen Z.Y.[...], Jenkins N.A.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCGenomics 36:431-439 (1996)Cited in2Mapped to99+
Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells.El-Amraoui A., Sahly I., Picaud S., Sahel J., Abitbol M., Petit C.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCHum. Mol. Genet. 5:1171-1178 (1996)Cited in1Mapped to8
Vertebrate unconventional myosins.Hasson T., Mooseker M.S.CategoriesFunctionSourceMGI: 104510PubMedEurope PMCJ Biol Chem 271:16431-16434 (1996)Mapped to36
Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13.Johnson K.R., Smith L., Johnson D.K., Rhodes J., Rinchik E.M., Thayer M., Lewis E.J.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCGenomics 33:527-531 (1996)Cited in1Mapped to29
Influence of gene duplication and X-inactivation on mouse mitochondrial malic enzyme activity and electrophoretic patterns.Eicher E.M., Coleman D.I.View abstractCategoriesSequences, ExpressionSourceMGI: 104510PubMedEurope PMCGenetics 85:647-658 (1977)Mapped to15
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.Weil D., Levy G., Sahly I., Levi-Acobas F., Blanchard S., El-Amraoui A., Crozet F., Philippe H., Abitbol M., Petit C.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 93:3232-3237 (1996)Cited in1Mapped to8
Deletion mapping of the chocolate (cht) locus within the Fes-Hbb region of mouse chromosome 7.Potter M.D., Rinchik E.M.CategoriesSequencesSourceMGI: 104510PubMedEurope PMCMamm Genome 4:46-48 (1993)Mapped to27
Deletion mapping of four loci defined by N-ethyl-N-nitrosourea-induced postimplantation-lethal mutations within the pid-Hbb region of mouse chromosome 7.Rinchik E.M., Carpenter D.A., Long C.L.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 104510PubMedEurope PMCGenetics 135:1117-1123 (1993)Mapped to22
Molecular analysis of radiation-induced albino (c)-locus mutations that cause death at preimplantation stages of development.Rinchik E.M., Tonjes R.R., Paul D., Potter M.D.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCGenetics 135:1107-1116 (1993)Mapped to15
Sequencing of the olfactory marker protein gene in normal and shaker-1 mutant mice.Brown K.A., Sutcliffe M.J., Steele K., Brown S.D.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCMamm. Genome 5:11-14 (1994)Cited in1Mapped to10
A type VII myosin encoded by the mouse deafness gene shaker-1.Gibson F., Walsh J., Mburu P., Varela A., Brown K.A., Antonio M., Beisel K.W., Steel K.P., Brown S.D.M.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCNature 374:62-64 (1995)Cited in1Mapped to10