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Strain Name:

SH1/LeJ

Stock Number:

000271

Availability:

Repository-Cryopreserved


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Additional References

 

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Bhattacharya C; Aggarwal S; Zhu R; Kumar M; Zhao M; Meistrich ML; Matin A. 2007. The mouse dead-end gene isoform alpha is necessary for germ cell and embryonic viability. Biochem Biophys Res Commun 355(1):194-9. [PubMed: 17291453]  [MGI Ref ID J:118625]

Bossi G; Booth S; Clark R; Davis EG; Liesner R; Richards K; Starcevic M; Stinchcombe J; Trambas C; Dell'Angelica EC; Griffiths GM. 2005. Normal lytic granule secretion by cytotoxic T lymphocytes deficient in BLOC-1, -2 and -3 and myosins Va, VIIa and XV. Traffic 6(3):243-51. [PubMed: 15702992]  [MGI Ref ID J:105404]

Cabraja M; Baurle J. 2007. Vestibular ganglion neurons survive hair cell defects in jerker, shaker, and Varitint-waddler mutants and downregulate calretinin expression. J Comp Neurol 504(4):418-26. [PubMed: 17663432]  [MGI Ref ID J:132913]

DEOL MS. 1956. The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. Proc R Soc Lond B Biol Sci 145(919):206-13. [PubMed: 13336002]  [MGI Ref ID J:13130]

Deol MS; Green MC. 1969. Cattanach's translocation as a tool for studying the action of the shaker-1 gene in the mouse. J Exp Zool 170(3):301-9. [PubMed: 5795329]  [MGI Ref ID J:5118]

Dunn LC. 1936. Studies on multiple allelomorphic series in the house mouse. I. Description of agouti and albino series of allelomorphs J Genet 33:443-53.  [MGI Ref ID J:22600]

El-Amraoui A; Petit C. 2005. Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells. J Cell Sci 118(Pt 20):4593-603. [PubMed: 16219682]  [MGI Ref ID J:102194]

Errijgers V; Van Dam D; Gantois I; Van Ginneken CJ; Grossman AW; D'Hooge R; De Deyn PP; Kooy RF. 2007. FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant, a sighted variant of the FVB/N mouse strain suitable for behavioral analysis. Genes Brain Behav 6(6):552-7. [PubMed: 17083330]  [MGI Ref ID J:137779]

Feldman HW. 1935. A fifth allelomorph in the albino series of the house mouse J Mammal 16:207-210.  [MGI Ref ID J:83666]

Feldman HW. 1922. A fourth allelomorph in the albino series in mice Am Naturalist 56:573-574.  [MGI Ref ID J:14850]

Futter CE; Ramalho JS; Jaissle GB; Seeliger MW; Seabra MC. 2004. The role of Rab27a in the regulation of melanosome distribution within retinal pigment epithelial cells. Mol Biol Cell 15(5):2264-75. [PubMed: 14978221]  [MGI Ref ID J:91408]

Gibson F; Walsh J; Mburu P; Varela A; Brown KA; Antonio M; Beisel KW; Steel KP; Brown SD. 1995. A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374(6517):62-4. [PubMed: 7870172]  [MGI Ref ID J:23257]

Hasson T; Walsh J; Cable J; Mooseker MS; Brown SD; Steel KP. 1997. Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression. Cell Motil Cytoskeleton 37(2):127-38. [PubMed: 9186010]  [MGI Ref ID J:42644]

Jones SM; Johnson KR; Yu H; Erway LC; Alagramam KN; Pollak N; Jones TA. 2005. A quantitative survey of gravity receptor function in mutant mouse strains. J Assoc Res Otolaryngol 6(4):297-310. [PubMed: 16235133]  [MGI Ref ID J:116914]

KOCHER W. 1960. [Studies on the genetics and pathology of the development of 8 labyrinth mutants (deaf-waltzer-shaker mutants) in the mouse (Mus musculus).] Z Vererbungsl 91:114-40. [PubMed: 13853422]  [MGI Ref ID J:15164]

Kikuchi K; Hilding DA. 1965. The defective organ of Corti in Shaker-1 mice Acta Otolaryngol (Stockh) 60:287-303.  [MGI Ref ID J:14846]

Klebig ML; Kwon BS; Rinchik EM. 1992. Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development. Mamm Genome 2(1):51-63. [PubMed: 1543902]  [MGI Ref ID J:1540]

Laiosa MD; Lai ZW; Thurmond TS; Fiore NC; DeRossi C; Holdener BC; Gasiewicz TA; Silverstone AE. 2002. 2,3,7,8-tetrachlorodibenzo-p-dioxin causes alterations in lymphocyte development and thymic atrophy in hemopoietic chimeras generated from mice deficient in ARNT2. Toxicol Sci 69(1):117-24. [PubMed: 12215665]  [MGI Ref ID J:113951]

Lamoreux ML; Wakamatsu K; Ito S. 2001. Interaction of major coat color gene functions in mice as studied by chemical analysis of eumelanin and pheomelanin. Pigment Cell Res 14(1):23-31. [PubMed: 11277491]  [MGI Ref ID J:103803]

Liu X; Ondek B; Williams DS. 1998. Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice [letter] Nat Genet 19(2):117-8. [PubMed: 9620764]  [MGI Ref ID J:48237]

Liu X; Udovichenko IP; Brown SD; Steel KP; Williams DS. 1999. Myosin VIIa participates in opsin transport through the photoreceptor cilium. J Neurosci 19(15):6267-74. [PubMed: 10414956]  [MGI Ref ID J:56998]

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Lossie AC; Nakamura H; Thomas SE; Justice MJ. 2005. Mutation of l7Rn3 shows that Odz4 is required for mouse gastrulation. Genetics 169(1):285-99. [PubMed: 15489520]  [MGI Ref ID J:96673]

Lyon MF. 1963. Attempts to test the inactive-X theory of dosage compensation in mammals Genet Res 4:93-103.  [MGI Ref ID J:272]

MIKAELIAN DO; RUBEN RJ. 1964. HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY. Arch Otolaryngol 80:418-30. [PubMed: 14198707]  [MGI Ref ID J:14858]

Mburu P; Liu XZ; Walsh J; Saw D Jr; Cope MJ; Gibson F; Kendrick-Jones J; Steel KP; Brown SD. 1997. Mutation analysis of the mouse myosin VIIA deafness gene. Genes Funct 1(3):191-203. [PubMed: 9680294]  [MGI Ref ID J:49926]

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Rhodes CR; Hertzano R; Fuchs H; Bell RE; de Angelis MH; Steel KP; Avraham KB. 2004. A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment. Mamm Genome 15(9):686-97. [PubMed: 15389316]  [MGI Ref ID J:93998]

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Sun JC; van Alphen AM; Wagenaar M; Huygen P; Hoogenraad CC; Hasson T; Koekkoek SK; Bohne BA; De Zeeuw CI. 2001. Origin of vestibular dysfunction in Usher syndrome type 1B. Neurobiol Dis 8(1):69-77. [PubMed: 11162241]  [MGI Ref ID J:110706]

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Tan Creti DM. 1969. Neuropathology of mutant mice with auditory and/or vestibular deficiencies J Neuropathol Exp Neurol 28:159.  [MGI Ref ID J:14891]

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Vasiliou V; Reuter SF; Nebert DW. 1997. Extrahepatic expression of NAD(P)H:menadione oxidoreductase, UDP glucuronosyltransferase-1A6, microsomal aldehyde dehydrogenase, and hepatic nuclear factor-1 alpha mRNAs in ch/ch and 14CoS/14CoS mice. Biochem Biophys Res Commun 233(3):631-6. [PubMed: 9168903]  [MGI Ref ID J:40515]

 

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