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Volumn 44, Issue 3, 1997, Pages 266-272

mdfw: A deafness susceptibility locus that interacts with deaf waddler (dfw)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN STEM RESPONSE; CHROMOSOME 10; CHROMOSOME 6; FEMALE; GENE LOCUS; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENOTYPE; HEARING IMPAIRMENT; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; SOUND PRESSURE;

EID: 0031572317     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4869     Document Type: Article
Times cited : (95)

References (17)
  • 1
    • 0028803112 scopus 로고
    • The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
    • Avraham, K. B., Hasson, T., Steel, K. P., Kingsley, D. M., Russell, L. B., Mooseker, M. S., Copeland, N. G., and Jenkins, N. A. (1995). The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells. Nature Genet. 11: 369-375.
    • (1995) Nature Genet. , vol.11 , pp. 369-375
    • Avraham, K.B.1    Hasson, T.2    Steel, K.P.3    Kingsley, D.M.4    Russell, L.B.5    Mooseker, M.S.6    Copeland, N.G.7    Jenkins, N.A.8
  • 2
    • 0028555358 scopus 로고
    • A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval
    • Chaib, H., Lina, G. G., Guilford, P., Plauchu, H., Levilliers, J., Morgon, A., and Petit, C. (1994). A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval. Hum. Mol. Genet. 3: 2219-2222.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 2219-2222
    • Chaib, H.1    Lina, G.G.2    Guilford, P.3    Plauchu, H.4    Levilliers, J.5    Morgon, A.6    Petit, C.7
  • 4
    • 0000870234 scopus 로고
    • The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse
    • Deol, M. S. (1955). The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. Proc. R. Soc. 145: 206-213.
    • (1955) Proc. R. Soc. , vol.145 , pp. 206-213
    • Deol, M.S.1
  • 5
    • 0013985845 scopus 로고
    • Snell's waltzer, a new mutation affecting behavior and the inner ear in the mouse
    • Deol, M. S., and Green, M. C. (1966). Snell's waltzer, a new mutation affecting behavior and the inner ear in the mouse Genet. Res. 8: 339-345.
    • (1966) Genet. Res. , vol.8 , pp. 339-345
    • Deol, M.S.1    Green, M.C.2
  • 6
    • 0029944722 scopus 로고    scopus 로고
    • The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction
    • Ebersole, T. A., Chen, Q., Justice, M. J., and Artzt, K. (1996). The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction. Nature Genet. 12: 260-265.
    • (1996) Nature Genet. , vol.12 , pp. 260-265
    • Ebersole, T.A.1    Chen, Q.2    Justice, M.J.3    Artzt, K.4
  • 7
    • 0027392717 scopus 로고
    • Genetics of age-related hearing loss in mice. I. Inbred and F1 hybrid strains
    • Erway, L. C., Willott, J. F., Archer, J. R., and Harrison, D. E. (1993). Genetics of age-related hearing loss in mice. I. Inbred and F1 hybrid strains. Hear. Res. 65: 125-132.
    • (1993) Hear. Res. , vol.65 , pp. 125-132
    • Erway, L.C.1    Willott, J.F.2    Archer, J.R.3    Harrison, D.E.4
  • 9
    • 0028306509 scopus 로고
    • A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene
    • Guilford, P., Ayadi, H., Blanchard, S., Chaib, H., Le, P. D., Weissenbach, J., Drira, M., and Petit, C. (1994). A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum. Mol. Genet. 3: 989-993.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 989-993
    • Guilford, P.1    Ayadi, H.2    Blanchard, S.3    Chaib, H.4    Le, P.D.5    Weissenbach, J.6    Drira, M.7    Petit, C.8
  • 10
    • 0001743627 scopus 로고
    • Deaf waddler (dfw)
    • Lane, P. W. (1987). Deaf waddler (dfw). Mouse News Lett. 77: 129.
    • (1987) Mouse News Lett. , vol.77 , pp. 129
    • Lane, P.W.1
  • 11
    • 0027355585 scopus 로고
    • A Macintosh program for storage and analysis of experimental genetic mapping data
    • Manly, K. F. (1993). A Macintosh program for storage and analysis of experimental genetic mapping data. Mamm. Genome 4: 303-313.
    • (1993) Mamm. Genome , vol.4 , pp. 303-313
    • Manly, K.F.1
  • 12
    • 0003928476 scopus 로고    scopus 로고
    • The Jackson Laboratory, Bar Harbor, ME
    • Mouse Genome Database (MGD) (1997). "Mouse Genome Informatics Project," The Jackson Laboratory, Bar Harbor, ME.
    • (1997) Mouse Genome Informatics Project
  • 14
    • 0029562474 scopus 로고
    • Inherited hearing defects in mice
    • Steel, K. P. (1995). Inherited hearing defects in mice. Annu. Rev. Genet. 29: 675-701.
    • (1995) Annu. Rev. Genet. , vol.29 , pp. 675-701
    • Steel, K.P.1
  • 15
    • 0029151628 scopus 로고
    • Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations
    • Street, V. A., Robinson, L. C., Erford, S. K., and Tempel, B. L. (1995). Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations. Genomics 29: 123-130.
    • (1995) Genomics , vol.29 , pp. 123-130
    • Street, V.A.1    Robinson, L.C.2    Erford, S.K.3    Tempel, B.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.