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
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 abstractCategoriesPhenotypes & 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
Defective myosin VIIA gene responsible for Usher syndrome type 1B.Weil D., Blanchard S., Kaplan J., Guilford P., Gibson F., Walsh J., Mburu P., Varela A., Levilliers J.[...], Petit C.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCNature 374:60-61 (1995)Cited in1Mapped to8
Genetic deafness--progress with mouse models.Brown S.D., Steel K.P.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCHum Mol Genet 3 Spec No:1453-1456 (1994)Mapped to8
Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B.Hasson T., Heintzelman M.B., Santos-Sacchi J., Corey D.P., Mooseker M.S.View abstractCategoriesSequences, ExpressionSourceMGI: 104510PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 92:9815-9819 (1995)Cited in2Mapped to8
The pattern of sensorineural degeneration in the cochlea of the deaf shaker-1 mouse: ultrastructural observations.Shnerson A., Lenoir M., van de Water T.R., Pujol R.View abstractCategoriesExpressionSourceMGI: 104510PubMedEurope PMCBrain Res 285:305-315 (1983)Mapped to8
Genetics of warfarin-resistance in house mice of three separate localities.MacSwiney F.J., Wallace M.E.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 104510PubMedEurope PMCJ Hyg (Lond) 80:69-75 (1978)Mapped to26
Cattanach's translocation as a tool for studying the action of the shaker- 1 gene in the mouse.Deol M.S., Green M.C.CategoriesFunction, SequencesSourceMGI: 104510PubMedEurope PMCJ Exp Zool 170:301-309 (1969)Mapped to8