메뉴 건너뛰기




Volumn 59, Issue 1, 2010, Pages 57-71

Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse

Author keywords

Deafness; Inner ear hair cell; Mouse mutant; Myosin VI; Stereocilia

Indexed keywords

MYOSIN VI;

EID: 77950650456     PISSN: 13411357     EISSN: None     Source Type: Journal    
DOI: 10.1538/expanim.59.57     Document Type: Article
Times cited : (11)

References (33)
  • 2
    • 0035159856 scopus 로고    scopus 로고
    • The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
    • Alagramam, K.N., Murcia, C.L., Kwon, H.Y., Pawlowski, K.S., Wright, C.G., and Woychik, R.P. 2001. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene. Nat. Genet. 27: 99-102.
    • (2001) Nat. Genet , vol.27 , pp. 99-102
    • Alagramam, K.N.1    Murcia, C.L.2    Kwon, H.Y.3    Pawlowski, K.S.4    Wright, C.G.5    Woychik, R.P.6
  • 3
    • 0036806216 scopus 로고    scopus 로고
    • A compendium of mouse knockouts with inner ear defects
    • Anagnostopoulos, A.V. 2002. A compendium of mouse knockouts with inner ear defects. Trends Genet. 18: S21-38.
    • (2002) Trends Genet , vol.18
    • Anagnostopoulos, A.V.1
  • 4
    • 0000286154 scopus 로고    scopus 로고
    • Disorders of free sialic acid storage
    • 8th ed. (Scriver, C.R., Beauded, A.L., Sly, W.E., and Valle, D. eds.), McGraw-Hill, New York
    • Aula, P. and Gahl, W.A. 2001. Disorders of free sialic acid storage. pp. 5109-5120. In: The Metabolic and Molecular Bases of Inherited Disease, 8th ed. (Scriver, C.R., Beauded, A.L., Sly, W.E., and Valle, D. eds.), McGraw-Hill, New York.
    • (2001) The Metabolic and Molecular Bases of Inherited Disease , pp. 5109-5120
    • Aula, P.1    Gahl, W.A.2
  • 5
    • 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. 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    Mooseker, M.S.6    Copeland, N.G.7    Jenkins, N.A.8
  • 6
    • 40849106619 scopus 로고    scopus 로고
    • Quiet as a mouse: Dissecting the molecular and genetic basis of hearing
    • Brown, S.D., Hardisty-Hughes, R.E., and Mburu, P. 2008. Quiet as a mouse: dissecting the molecular and genetic basis of hearing. Nat. Rev. Genet. 9: 277-290.
    • (2008) Nat. Rev. Genet , vol.9 , pp. 277-290
    • Brown, S.D.1    Hardisty-Hughes, R.E.2    Mburu, P.3
  • 7
    • 33846359680 scopus 로고    scopus 로고
    • Myosin VI and VIIa distribution among inner ear epithelia in diverse ishes
    • Cofin, A.B., Dabdoub, A., Kelley, M.W., and Popper, A.N. 2007. Myosin VI and VIIa distribution among inner ear epithelia in diverse ishes. Hear. Res. 224: 15-26.
    • (2007) Hear. Res , vol.224 , pp. 15-26
    • Cofin, A.B.1    Dabdoub, A.2    Kelley, M.W.3    Popper, A.N.4
  • 8
    • 0035168151 scopus 로고    scopus 로고
    • Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
    • Di Palma, F., Holme, R.H., Bryda, E.C., Belyantseva, I.A., Pellegrino, R., Kachar, B., Steel, K.P., and Noben-Trauth, K. 2001. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nat. Genet. 27: 103-107.
    • (2001) Nat. Genet , vol.27 , pp. 103-107
    • di Palma, F.1    Holme, R.H.2    Bryda, E.C.3    Belyantseva, I.A.4    Pellegrino, R.5    Kachar, B.6    Steel, K.P.7    Noben-Trauth, K.8
  • 9
    • 0035828440 scopus 로고    scopus 로고
    • Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: Questionnaire based ascertainment study
    • Fortnum, H.M., Summerield, A.Q., Marshall, D.H., Davis, A.C., and Bamford, J.M. 2001. Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment study. BMJ 323: 536-540.
    • (2001) BMJ , vol.323 , pp. 536-540
    • Fortnum, H.M.1    Summerield, A.Q.2    Marshall, D.H.3    Davis, A.C.4    Bamford, J.M.5
  • 10
    • 36048955489 scopus 로고    scopus 로고
    • Mouse models to study inner ear development and hereditary hearing loss
    • Friedman, L.M., Dror, A.A., and Avraham, K.B. 2007. Mouse models to study inner ear development and hereditary hearing loss. Int. J. Dev. Biol. 51: 609-631.
    • (2007) Int. J. Dev. Biol , vol.51 , pp. 609-631
    • Friedman, L.M.1    Dror, A.A.2    Avraham, K.B.3
  • 13
    • 34250858976 scopus 로고    scopus 로고
    • Auditory transduction in the mouse
    • Grant, L. and Fuchs, P.A. 2007. Auditory transduction in the mouse. Plugers Arch. 454: 793-804.
    • (2007) Plugers Arch , vol.454 , pp. 793-804
    • Grant, L.1    Fuchs, P.A.2
  • 14
    • 77950663340 scopus 로고
    • New mutant-Snell's waltzer-sv
    • Green, M.C. 1960. New mutant-Snell's waltzer-sv. Mouse News Lett. 23: 40.
    • (1960) Mouse News Lett , vol.23 , pp. 40
    • Green, M.C.1
  • 15
    • 0027993176 scopus 로고
    • Porcine myosin-VI: Characterization of a new mammalian unconventional myosin
    • Hasson, T. and Mooseker, M.S. 1994. Porcine myosin-VI: characterization of a new mammalian unconventional myosin. J. Cell Biol. 127: 425-440.
    • (1994) J. Cell Biol , vol.127 , pp. 425-440
    • Hasson, T.1    Mooseker, M.S.2
  • 18
    • 42649108717 scopus 로고    scopus 로고
    • A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss
    • Hilgert, N., Topsakal, V., van Dinther, J., Offeciers, E., Van de Heyning, P., and Van Camp, G. 2008. A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss. Eur. J. Hum. Genet. 16: 593-602.
    • (2008) Eur. J. Hum. Genet , vol.16 , pp. 593-602
    • Hilgert, N.1    Topsakal, V.2    van Dinther, J.3    Offeciers, E.4    van de Heyning, P.5    van Camp, G.6
  • 19
    • 33644752095 scopus 로고    scopus 로고
    • Myosin VI is a mediator of the p53-dependent cell survival pathway
    • Jung, E.J., Liu, G., Zhou, W., and Chen, X. 2006. Myosin VI is a mediator of the p53-dependent cell survival pathway. Mol. Cell. Biol. 26: 2175-2186.
    • (2006) Mol. Cell. Biol , vol.26 , pp. 2175-2186
    • Jung, E.J.1    Liu, G.2    Zhou, W.3    Chen, X.4
  • 22
    • 13544276523 scopus 로고    scopus 로고
    • Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium
    • Kikkawa, Y., Mburu, P., Morse, S., Kominami, R., Townsend, S., and Brown, S.D. 2005. Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium. Hum. Mol. Genet. 14: 391-400.
    • (2005) Hum. Mol. Genet , vol.14 , pp. 391-400
    • Kikkawa, Y.1    Mburu, P.2    Morse, S.3    Kominami, R.4    Townsend, S.5    Brown, S.D.6
  • 23
    • 27644507327 scopus 로고    scopus 로고
    • Hair-cell mechanotransduction and cochlear ampliication
    • LeMasurier, M. and Gillespie, P.G. 2005. Hair-cell mechanotransduction and cochlear ampliication. Neuron 48: 403-415.
    • (2005) Neuron , vol.48 , pp. 403-415
    • Lemasurier, M.1    Gillespie, P.G.2
  • 24
    • 0035164656 scopus 로고    scopus 로고
    • Map Manager QTX, cross-platform software for genetic mapping
    • Manly, K.F., Cudmore, R.H. Jr., and Meer, J.M. 2001. Map Manager QTX, cross-platform software for genetic mapping. Mamm. Genome 12: 930-932
    • (2001) Mamm. Genome , vol.12 , pp. 930-932
    • Manly, K.F.1    Cudmore Jr., R.H.2    Meer, J.M.3
  • 27
    • 32044471289 scopus 로고    scopus 로고
    • From deafness genes to hearing mechanisms: Harmony and counterpoint
    • Petit, C. 2006. From deafness genes to hearing mechanisms: harmony and counterpoint. Trends Mol. Med. 12: 57-64.
    • (2006) Trends Mol. Med , vol.12 , pp. 57-64
    • Petit, C.1
  • 29
    • 1642322799 scopus 로고    scopus 로고
    • An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal
    • Rzadzinska, A.K., Schneider, M.E., Davies, C., Riordan, G.P., and Kachar, B. 2004. An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal. J. Cell Biol. 164: 887-897.
    • (2004) J. Cell Biol , vol.164 , pp. 887-897
    • Rzadzinska, A.K.1    Schneider, M.E.2    Davies, C.3    Riordan, G.P.4    Kachar, B.5
  • 32
    • 34547700102 scopus 로고    scopus 로고
    • The micromachinery of mechanotransduction in hair cells
    • Vollrath, M.A., Kwan, K.Y., and Corey, D.P. 2007. The micromachinery of mechanotransduction in hair cells. Annu. Rev. Neurosci. 30: 339-365.
    • (2007) Annu. Rev. Neurosci , vol.30 , pp. 339-365
    • Vollrath, M.A.1    Kwan, K.Y.2    Corey, D.P.3
  • 33
    • 0034604349 scopus 로고    scopus 로고
    • The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins
    • Zheng, L., Sekerková, G., Vranich, K., Tilney, L.G., Mugnaini, E., and Bartles, J.R. 2000. The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins. Cell 102: 377-385.
    • (2000) Cell , vol.102 , pp. 377-385
    • Zheng, L.1    Sekerková, G.2    Vranich, K.3    Tilney, L.G.4    Mugnaini, E.5    Bartles, J.R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.