메뉴 건너뛰기




Volumn 63, Issue 5, 1998, Pages 1263-1270

Development and maintenance of ear innervation and function: Lessons from mutations in mouse and man

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN DERIVED NEUROTROPHIC FACTOR; MYOSIN;

EID: 0032231891     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302126     Document Type: Article
Times cited : (9)

References (31)
  • 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 KB, Hasson T, Steel KP, Kingsley DM, Russell LB, Mooseker MS, Copeland NG, 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    Mooseker, M.S.6    Copeland, N.G.7
  • 4
    • 0031983347 scopus 로고    scopus 로고
    • Genetic causes of hearing loss
    • Cremers FPM (1998) Genetic causes of hearing loss. Curr Opin Neurol 11:11-16
    • (1998) Curr Opin Neurol , vol.11 , pp. 11-16
    • Cremers, F.P.M.1
  • 8
    • 0343471382 scopus 로고    scopus 로고
    • Lack of NT-3 causes losses of both classes of spiral ganglion neurons in the cochlea in a region specific fashion
    • Fritzsch B, Fariñas I, Reichardt LF (1997a) Lack of NT-3 causes losses of both classes of spiral ganglion neurons in the cochlea in a region specific fashion. J Neurosci 17:6213-6225
    • (1997) J Neurosci , vol.17 , pp. 6213-6225
    • Fritzsch, B.1    Fariñas, I.2    Reichardt, L.F.3
  • 9
    • 0030859146 scopus 로고    scopus 로고
    • Mice lacking the neurotrophin receptor trkB lose their specific afferent innervation but do develop taste buds
    • Fritzsch B, Sarai PA, Barbacid M, Silos-Santiago I (1997b) Mice lacking the neurotrophin receptor trkB lose their specific afferent innervation but do develop taste buds. Int J Dev Neurosci 15:563-576
    • (1997) Int J Dev Neurosci , vol.15 , pp. 563-576
    • Fritzsch, B.1    Sarai, P.A.2    Barbacid, M.3    Silos-Santiago, I.4
  • 11
    • 0031894362 scopus 로고    scopus 로고
    • Hoxal and Hoxb1 synergize in patterning the hindbrain, cranial nerves and second pharyngeal arch
    • Gavalas A, Studer M, Lumsden A, Rijli FM, Krumlauf R, Chambon P (1998) Hoxal and Hoxb1 synergize in patterning the hindbrain, cranial nerves and second pharyngeal arch. Development 125:1123-1136
    • (1998) Development , vol.125 , pp. 1123-1136
    • Gavalas, A.1    Studer, M.2    Lumsden, A.3    Rijli, F.M.4    Krumlauf, R.5    Chambon, P.6
  • 13
    • 0031889394 scopus 로고    scopus 로고
    • Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: A candidate for human autosomal dominant nonsyndromic deafness
    • Hughes DC, Legan PK, Steel KP, Richardson GP (1998) Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness. Genomics 48:46-51
    • (1998) Genomics , vol.48 , pp. 46-51
    • Hughes, D.C.1    Legan, P.K.2    Steel, K.P.3    Richardson, G.P.4
  • 14
    • 15844369925 scopus 로고    scopus 로고
    • Mutations in the trkA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis
    • Indo Y, Tsuruta M, Hayashida Y, Karim MA, Ohta K, Kawano T, Mitsubuchi H, et al (1996) Mutations in the trkA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis. Nat Genet 13:485-488
    • (1996) Nat Genet , vol.13 , pp. 485-488
    • Indo, Y.1    Tsuruta, M.2    Hayashida, Y.3    Karim, M.A.4    Ohta, K.5    Kawano, T.6    Mitsubuchi, H.7
  • 15
    • 0030889074 scopus 로고    scopus 로고
    • The mouse tectorins: Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system
    • Legan PK, Rau A, Keen JN, Richardson GP (1997) The mouse tectorins: modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system. J Biol Chem 272:8791-8801
    • (1997) J Biol Chem , vol.272 , pp. 8791-8801
    • Legan, P.K.1    Rau, A.2    Keen, J.N.3    Richardson, G.P.4
  • 17
    • 0032032016 scopus 로고    scopus 로고
    • Neurogenin-1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia
    • Ma Q, Chen Z, del Barco Barantes I, Barrantes I, de la Pompa JL, Andersen DJ (1998) Neurogenin-1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia. Neuron 20:469-482
    • (1998) Neuron , vol.20 , pp. 469-482
    • Ma, Q.1    Chen, Z.2    Del Barco Barantes, I.3    Barrantes, I.4    De la Pompa, J.L.5    Andersen, D.J.6
  • 19
    • 0032079370 scopus 로고    scopus 로고
    • Development of the mouse inner ear and origin of its sensory organs
    • Morsli H, Choo D, Ryan A, Johnson R, Wu DK (1998) Development of the mouse inner ear and origin of its sensory organs. J Neurosci 18:3327-3335
    • (1998) J Neurosci , vol.18 , pp. 3327-3335
    • Morsli, H.1    Choo, D.2    Ryan, A.3    Johnson, R.4    Wu, D.K.5
  • 20
    • 0031054075 scopus 로고    scopus 로고
    • A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
    • Neyroud N, Tesson F, Denjoy I, Leibovici M, Donger C, Barhanin J, Faure S, et al (1997) A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nat Genet 15:186-1891
    • (1997) Nat Genet , vol.15 , pp. 186-1891
    • Neyroud, N.1    Tesson, F.2    Denjoy, I.3    Leibovici, M.4    Donger, C.5    Barhanin, J.6    Faure, S.7
  • 22
    • 0031884319 scopus 로고    scopus 로고
    • 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 SD, Steel KP (1998) Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. Development 125:557-566
    • (1998) Development , vol.125 , pp. 557-566
    • Self, T.1    Mahony, M.2    Fleming, J.3    Walsh, J.4    Brown, S.D.5    Steel, K.P.6
  • 23
    • 0030696661 scopus 로고    scopus 로고
    • Severe sensory deficits but normal CNS development in newborn mice lacking TrkB and TrkC tyrosinc protein kinase receptors
    • Silos-Santiago I, Fagan AM, Garber M, Fritzsch B, Barbacid M (1997) Severe sensory deficits but normal CNS development in newborn mice lacking TrkB and TrkC tyrosinc protein kinase receptors. Eur J Neurosci 9:2045-2056
    • (1997) Eur J Neurosci , vol.9 , pp. 2045-2056
    • Silos-Santiago, I.1    Fagan, A.M.2    Garber, M.3    Fritzsch, B.4    Barbacid, M.5
  • 25
    • 0032007713 scopus 로고    scopus 로고
    • The development of the vertebrate inner ear
    • Torres M, Giraldez F (1998) The development of the vertebrate inner ear. Mech Dev 71:5-21
    • (1998) Mech Dev , vol.71 , pp. 5-21
    • Torres, M.1    Giraldez, F.2
  • 26
    • 9844261701 scopus 로고    scopus 로고
    • IsK and KvLQT1: Mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome
    • Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, et al (1997) IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome. Hum Mol Genet 6:2179-2185
    • (1997) Hum Mol Genet , vol.6 , pp. 2179-2185
    • Tyson, J.1    Tranebjaerg, L.2    Bellman, S.3    Wren, C.4    Taylor, J.F.5    Bathen, J.6    Aslaksen, B.7
  • 28
    • 0031978985 scopus 로고    scopus 로고
    • The molecular genetics of the long QT syndrome: Genes causing fainting and sudden death
    • Vincent GM (1998) The molecular genetics of the long QT syndrome: genes causing fainting and sudden death. Annu Rev Med 49:263-274
    • (1998) Annu Rev Med , vol.49 , pp. 263-274
    • Vincent, G.M.1
  • 29


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.