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Volumn 152, Issue 4, 1999, Pages 1691-1699

A new mouse insertional mutation that causes sensorineural deafness and vestibular defects

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 0344069721     PISSN: 00166731     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (29)

References (36)
  • 2
    • 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., T. HASSON, K. P. STEEL., D. M. KINGSLEY, L. B. RUSSELL et al., 1995 The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells. Nat. Genet. 11: 369-375.
    • (1995) Nat. 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
  • 3
    • 0021050913 scopus 로고
    • Double cos site vectors: Simplified cosmid cloning
    • BATES, P. F., and SWIFT, R. A. 1983 Double cos site vectors: simplified cosmid cloning. Gene 26: 137-146.
    • (1983) Gene , vol.26 , pp. 137-146
    • Bates, P.F.1    Swift, R.A.2
  • 4
    • 0027249595 scopus 로고
    • dbEST -database for expressed sequence tags
    • BOUGUSKI, M. S., T. M. LOWE and C. M.TOLSTOSHEV, 1993 dbEST -database for expressed sequence tags. Nat. Genet. 4: 332-333.
    • (1993) Nat. Genet. , vol.4 , pp. 332-333
    • Bouguski, M.S.1    Lowe, T.M.2    Tolstoshev, C.M.3
  • 5
    • 0031634650 scopus 로고    scopus 로고
    • Encyclopedia of the mouse genome VII. Mouse chromosome 10
    • Spec No. S200-14
    • BURMEISTKER, M., E. C. BRYDA, J. F. BUREAU and K. NOBEN-TRAUTH, 1998 Encyclopedia of the mouse genome VII. Mouse chromosome 10. Mamm. Genome 8: Spec No. S200-14.
    • (1998) Mamm. Genome , vol.8
    • Burmeistker, M.1    Bryda, E.C.2    Bureau, J.F.3    Noben-Trauth, K.4
  • 6
    • 0030054738 scopus 로고    scopus 로고
    • Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22
    • CHAIB, H., C. PLACE, N. SALEM, C. DODE, S. CHARDENOUX et al., 1996 Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22. Hum. Mol. Genet. 5: 1061-1064.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1061-1064
    • Chaib, H.1    Place, C.2    Salem, N.3    Dode, C.4    Chardenoux, S.5
  • 7
    • 0014292278 scopus 로고
    • Inherited disease of the inner ear in man in the light of studies on the mouse
    • DEOL., M. S., 1968 Inherited disease of the inner ear in man in the light of studies on the mouse. J. Med. Genet. 5: 137-158.
    • (1968) J. Med. Genet. , vol.5 , pp. 137-158
    • Deol, M.S.1
  • 8
    • 0027392717 scopus 로고
    • Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains
    • ERWAY, L., J. WILLOT, J. ARCHER and D. HARRISON, 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.1    Willot, J.2    Archer, J.3    Harrison, D.4
  • 10
    • 0028860302 scopus 로고
    • A type VII myosin encoded by the mouse deafness gene shaker-1
    • GIBSON, F., J. WALSH, P. MBURU, A. VARELA, K. A. BROWN et al., 1995 A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374: 62-64.
    • (1995) Nature , vol.374 , pp. 62-64
    • Gibson, F.1    Walsh, J.2    Mburu, P.3    Varela, A.4    Brown, K.A.5
  • 11
    • 0345556152 scopus 로고
    • Standardized nomenclature for transgenic animals
    • GORDON, J. 1992 Standardized nomenclature for transgenic animals. ILAR News 34: 45.
    • (1992) ILAR News , vol.34 , pp. 45
    • Gordon, J.1
  • 12
    • 0031683423 scopus 로고    scopus 로고
    • The fundamental and medical impacts of recent progress in research on hereditary hearing loss
    • KALATZIS, V., and C. PETIT, 1998 The fundamental and medical impacts of recent progress in research on hereditary hearing loss. Hum. Mol. Gen. 7: 1589-1597.
    • (1998) Hum. Mol. Gen. , vol.7 , pp. 1589-1597
    • Kalatzis, V.1    Petit, C.2
  • 13
    • 0024851396 scopus 로고
    • The primary structure of human liver type phosphofructokinase and its comparison with other types of PFK
    • LEVANON, D., E. DANCIGER, N. DAFNI, Y. BERNSTEIN, A. ELSON et al., 1989 The primary structure of human liver type phosphofructokinase and its comparison with other types of PFK. DNA 8: 733-743.
    • (1989) DNA , vol.8 , pp. 733-743
    • Levanon, D.1    Danciger, E.2    Dafni, N.3    Bernstein, Y.4    Elson, A.5
  • 14
    • 0030960855 scopus 로고    scopus 로고
    • Mutation in the myosin VIIA gene causes non-syndromic recessive deafness
    • LIU, X. Z., J. WALSH, Y. TAMAGAWA, K. KITAMURA, M. NISHIZAWA et al., 1997 Mutation in the myosin VIIA gene causes non-syndromic recessive deafness. Nat. Genet. 16: 188-190.
    • (1997) Nat. Genet. , vol.16 , pp. 188-190
    • Liu, X.Z.1    Walsh, J.2    Tamagawa, Y.3    Kitamura, K.4    Nishizawa, M.5
  • 15
    • 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
  • 16
    • 0026410464 scopus 로고
    • Genetic epidemiology of hearing impairment
    • MORTON, N. E. 1991 Genetic epidemiology of hearing impairment. Ann. NY Acad. Sci. 630: 16-31.
    • (1991) Ann. NY Acad. Sci. , vol.630 , pp. 16-31
    • Morton, N.E.1
  • 17
    • 0025821494 scopus 로고
    • A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis
    • MUCENSKI, M. L., K. MCLAIN, A. B. KIER, S. H. SWERDLOW, C. M. SCHREINER et al., 1991 A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis. Cell 65: 677-689.
    • (1991) Cell , vol.65 , pp. 677-689
    • Mucenski, M.L.1    McLain, K.2    Kier, A.B.3    Swerdlow, S.H.4    Schreiner, C.M.5
  • 18
    • 0026410409 scopus 로고
    • Comparative gene mapping, genome duplication, and the genetics of hearing
    • NADEAU, J. H., M. KOSOWSKY and K. P. STEEL, 1991 Comparative gene mapping, genome duplication, and the genetics of hearing. Ann. NY Acad. Sci. 630: 49-67.
    • (1991) Ann. NY Acad. Sci. , vol.630 , pp. 49-67
    • Nadeau, J.H.1    Kosowsky, M.2    Steel, K.P.3
  • 19
    • 0025989497 scopus 로고
    • Regional assignment of the human cell cycle control gene CDC2 to chromosome 10q21 by in situ hybridization
    • NAZARENKO, S. A., N. V. OSTROVERHOVA and N. K. SPURR, 1991 Regional assignment of the human cell cycle control gene CDC2 to chromosome 10q21 by in situ hybridization. Hum. Genet. 87: 621-622.
    • (1991) Hum. Genet. , vol.87 , pp. 621-622
    • Nazarenko, S.A.1    Ostroverhova, N.V.2    Spurr, N.K.3
  • 20
    • 0029807805 scopus 로고    scopus 로고
    • Genes responsible for human hereditary deafness: Symphony of a thousand
    • PETIT, C. 1996 Genes responsible for human hereditary deafness: symphony of a thousand. Nat. Genet. 14: 385-391.
    • (1996) Nat. Genet. , vol.14 , pp. 385-391
    • Petit, C.1
  • 21
    • 17644442703 scopus 로고    scopus 로고
    • Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene
    • PROBST, F. J., R. A. FRIDELL, Y. RAPHAEL, T. L. SAUNDERS, A. WANG et al., 1998 Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Science 280: 1444-1447.
    • (1998) Science , vol.280 , pp. 1444-1447
    • Probst, F.J.1    Fridell, R.A.2    Raphael, Y.3    Saunders, T.L.4    Wang, A.5
  • 23
    • 0028466229 scopus 로고
    • Insertional mutagenesis in transgenic mice
    • RIJKERS, T., A. PEETZ and U. RUTHER, 1994 Insertional mutagenesis in transgenic mice. Transgenic Res. 3: 203-215.
    • (1994) Transgenic Res. , vol.3 , pp. 203-215
    • Rijkers, T.1    Peetz, A.2    Ruther, U.3
  • 25
    • 0002475584 scopus 로고
    • Developmental defects
    • edited by R. K. BUSSEY, T. LAZAR and F. M. KLASS. Lea & Febiger, Philadelphia
    • SCHUKNECHT, H. F. 1993 Developmental defects, pp. 115-189 in Pathology of the Ear, edited by R. K. BUSSEY, T. LAZAR and F. M. KLASS. Lea & Febiger, Philadelphia.
    • (1993) Pathology of the Ear , pp. 115-189
    • Schuknecht, H.F.1
  • 26
    • 0021802841 scopus 로고
    • Fused transcript of abl and bcr genes in chronic myelogenous leukaemia
    • SHTIVELMAN, E., B. LIFSHITZ, R. P. GALE and E. CANAANI, 1985 Fused transcript of abl and bcr genes in chronic myelogenous leukaemia. Nature 315: 550-554.
    • (1985) Nature , vol.315 , pp. 550-554
    • Shtivelman, E.1    Lifshitz, B.2    Gale, R.P.3    Canaani, E.4
  • 27
    • 0025790346 scopus 로고
    • Legless insertional mutation: Morphological, molecular, and genetic characterization
    • SINGH, G., D. M. SUPP, C. SCHRKINER, J. MCNEISH, H.-J. MERKER et al., 1991 legless insertional mutation: morphological, molecular, and genetic characterization, Genes Dev. 5: 2245-2255.
    • (1991) Genes Dev. , vol.5 , pp. 2245-2255
    • Singh, G.1    Supp, D.M.2    Schrkiner, C.3    McNeish, J.4    Merker, H.-J.5
  • 28
    • 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
  • 29
    • 0025072673 scopus 로고
    • The murine genes Hox-5.1 and Hox-4.1 belong to the same HOX complex on chromosome 2
    • STUBBS, L., A. POUSTKA, A. BARON, H. LEHRACH, P. LONAI et al., 1990 The murine genes Hox-5.1 and Hox-4.1 belong to the same HOX complex on chromosome 2. Genomics 7: 422-427.
    • (1990) Genomics , vol.7 , pp. 422-427
    • Stubbs, L.1    Poustka, A.2    Baron, A.3    Lehrach, H.4    Lonai, P.5
  • 30
    • 0028587896 scopus 로고
    • Clustering of six human 11p1S gene homologs within a 500-kb interval of proximal mouse chromosome 7
    • STUBBS, L., E. M. RINCHIK, E. GOLDBERG, B. RUDY, M. A. HANDEL et al, 1994 Clustering of six human 11p1S gene homologs within a 500-kb interval of proximal mouse chromosome 7. Genomics 24: 324-332.
    • (1994) Genomics , vol.24 , pp. 324-332
    • Stubbs, L.1    Rinchik, E.M.2    Goldberg, E.3    Rudy, B.4    Handel, M.A.5
  • 31
    • 0030074586 scopus 로고    scopus 로고
    • The gene encoding the central cannabinoid receptor is located in proximal mouse chromosome 4
    • STUBBS, L., L. CHITTENDEN, A. CHAKRABARTI and E. ONAIVI, 1996 The gene encoding the central cannabinoid receptor is located in proximal mouse Chromosome 4. Mamm. Genome 7: 165-166.
    • (1996) Mamm. Genome , vol.7 , pp. 165-166
    • Stubbs, L.1    Chittenden, L.2    Chakrabarti, A.3    Onaivi, E.4
  • 33
    • 0032577293 scopus 로고    scopus 로고
    • Association of unconventional myosin MYOI5 mutations with human nonsyndromic deafness DFNB3
    • WANG, A., Y. LIANG, R. A. FRIDELL F. J. PROBST, E. R. WILCOX et al., 1998 Association of unconventional myosin MYOI5 mutations with human nonsyndromic deafness DFNB3. Science 280: 1447-1451.
    • (1998) Science , vol.280 , pp. 1447-1451
    • Wang, A.1    Liang, Y.2    Fridell, R.A.3    Probst, F.J.4    Wilcox, E.R.5
  • 34
    • 0028815440 scopus 로고
    • Defective myosin VIIA gene responsible for usher syndrome type 1B
    • WEIL, D., S. BLANCHARD, J. KAPLAN, P. GUILFORD, F. GIBSON et al., 1995 Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374: 60-61.
    • (1995) Nature , vol.374 , pp. 60-61
    • Weil, D.1    Blanchard, S.2    Kaplan, J.3    Guilford, P.4    Gibson, F.5
  • 35
    • 0030951102 scopus 로고    scopus 로고
    • The autosomal recessive isolated deafness, DFNB2, and the usher 1B syndrome are allelic defects of the myosin-VIIA gene
    • WEIL, D., P. KUSSEL, S. BLANCHARD, G. LEVY, F. LEVI-ACOBAS et al., 1997 The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. Nat. Genet. 16: 191-193.
    • (1997) Nat. Genet. , vol.16 , pp. 191-193
    • Weil, D.1    Kussel, P.2    Blanchard, S.3    Levy, G.4    Levi-Acobas, F.5
  • 36
    • 0022366933 scopus 로고
    • An inherited limb deformity created by insertional mutagenesis in a transgenic mouse
    • WOYCHIK, R. P., T. A. STEWART, L. G. DAVIS, P. D'EUSTACHIO and P. LEDER, 1985 An inherited limb deformity created by insertional mutagenesis in a transgenic mouse. Nature 318: 36-40.
    • (1985) Nature , vol.318 , pp. 36-40
    • Woychik, R.P.1    Stewart, T.A.2    Davis, L.G.3    D'Eustachio, P.4    Leder, P.5


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