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Volumn 15, Issue 4, 2010, Pages 247-253

Ultrastructural localization of cochlin in the rat cochlear duct

Author keywords

COCH gene; DFNA9; Hereditary hearing impairment; Immunogold method; Inner ear

Indexed keywords

COCHLIN PROTEIN, RAT; COLLAGEN TYPE 2; SCLEROPROTEIN;

EID: 77952953880     PISSN: 14203030     EISSN: 14219700     Source Type: Journal    
DOI: 10.1159/000256664     Document Type: Article
Times cited : (3)

References (34)
  • 3
    • 33644948652 scopus 로고    scopus 로고
    • Collagen changes in the cochlea of aged Fischer 344 rats
    • Buckiova D, Popelar J, Syka J: Collagen changes in the cochlea of aged Fischer 344 rats. Exp Gerontol 2006; 41: 296-302.
    • (2006) Exp Gerontol , vol.41 , pp. 296-302
    • Buckiova, D.1    Popelar, J.2    Syka, J.3
  • 5
    • 0035985784 scopus 로고    scopus 로고
    • The presence and arrangement of type II collagen in the basilar membrane
    • Dreiling FJ, Henson MM, Henson OW Jr: The presence and arrangement of type II collagen in the basilar membrane. Hear Res 2002; 166: 166-180.
    • (2002) Hear Res , vol.166 , pp. 166-180
    • Dreiling, F.J.1    Henson, M.M.2    Henson Jr., O.W.3
  • 7
    • 0141920801 scopus 로고    scopus 로고
    • Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin
    • Grabski R, Szul T, Sasaki T, Timpl R, Mayne R, Hicks B, Sztul E: Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin. Hum Genet 2003; 113:406-416.
    • (2003) Hum Genet , vol.113 , pp. 406-416
    • Grabski, R.1    Szul, T.2    Sasaki, T.3    Timpl, R.4    Mayne, R.5    Hicks, B.6    Sztul, E.7
  • 8
    • 0035953042 scopus 로고    scopus 로고
    • Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein
    • Ikezono T, Omori A, Ichinose S, Pawanker R, Watanabe A, Yagi T: Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein. Biochim Biophys Acta 2001; 1535:258-265.
    • (2001) Biochim Biophys Acta , vol.1535 , pp. 258-265
    • Ikezono, T.1    Omori, A.2    Ichinose, S.3    Pawanker, R.4    Watanabe, A.5    Yagi, T.6
  • 11
    • 0027942179 scopus 로고
    • Morphological changes in the tectorial and basilar membranes of aged rats
    • Ishii K, Murofushi T, Takeuchi N: Morphological changes in the tectorial and basilar membranes of aged rats. Eur Arch Otorhinolaryngol 1994; 251: 357-360.
    • (1994) Eur Arch Otorhinolaryngol , vol.251 , pp. 357-360
    • Ishii, K.1    Murofushi, T.2    Takeuchi, N.3
  • 12
    • 0028674954 scopus 로고
    • Ultrastructural and immunocyto-chemical study of the subepithelial fiber component of the guinea pig inner ear
    • Kaname H, Yoshihara T, Ishii T, Tatsuoka H, Chiba T: Ultrastructural and immunocyto-chemical study of the subepithelial fiber component of the guinea pig inner ear. J Electron Microsc 1994; 43:394-397.
    • (1994) J Electron Microsc , vol.43 , pp. 394-397
    • Kaname, H.1    Yoshihara, T.2    Ishii, T.3    Tatsuoka, H.4    Chiba, T.5
  • 13
    • 0026229783 scopus 로고
    • Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds
    • Khetarpal U, Schuknecht HF, Gacek RR, Holmes LB: Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds. Arch Otolaryngol Head Neck Surg 1991; 117: 1032-1042.
    • (1991) Arch Otolaryngol Head Neck Surg , vol.117 , pp. 1032-1042
    • Khetarpal, U.1    Schuknecht, H.F.2    Gacek, R.R.3    Holmes, L.B.4
  • 14
    • 0027475671 scopus 로고
    • Autosomal dominant sensorineural hearing loss. Further temporal bone findings
    • Khetarpal U: Autosomal dominant sensorineural hearing loss. Further temporal bone findings. Arch Otolaryngol Head Neck Surg 1993; 119:106-108.
    • (1993) Arch Otolaryngol Head Neck Surg , vol.119 , pp. 106-108
    • Khetarpal, U.1
  • 15
    • 0033883414 scopus 로고    scopus 로고
    • DFNA9 is a progressive audiovestibular dysfunction with a microfibrillar deposit in the inner ear
    • Khetarpal U: DFNA9 is a progressive audiovestibular dysfunction with a microfibrillar deposit in the inner ear. Laryngoscope 2000; 110:1379-1384.
    • (2000) Laryngoscope , vol.110 , pp. 1379-1384
    • Khetarpal, U.1
  • 19
    • 56649115858 scopus 로고    scopus 로고
    • The second von Willebrand type A domain of cochlin has high affinity for type I, type II and type IV collagens
    • Nagy I, Trexler M, Patthy L: The second von Willebrand type A domain of cochlin has high affinity for type I, type II and type IV collagens. FEBS Lett 2008; 582: 4003-4007.
    • (2008) FEBS Lett , vol.582 , pp. 4003-4007
    • Nagy, I.1    Trexler, M.2    Patthy, L.3
  • 22
    • 0037488241 scopus 로고    scopus 로고
    • Subcellular localization, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9
    • Robertson NG, Hamaker SA, Patriub V, Aster JC, Morton CC: Subcellular localization, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9. J Med Genet 2003; 40: 479-486.
    • (2003) J Med Genet , vol.40 , pp. 479-486
    • Robertson, N.G.1    Hamaker, S.A.2    Patriub, V.3    Aster, J.C.4    Morton, C.C.5
  • 28
    • 0026631641 scopus 로고
    • Localization of type II, IX and V collagen in the inner ear
    • Slepecky NB, Savage JE, Yoo TJ: Localization of type II, IX and V collagen in the inner ear. Acta Otolaryngol 1992; 112: 611-617.
    • (1992) Acta Otolaryngol , vol.112 , pp. 611-617
    • Slepecky, N.B.1    Savage, J.E.2    Yoo, T.J.3
  • 29
    • 10744220263 scopus 로고    scopus 로고
    • Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochlea-vestibular dysfunction, but not of Ménière's disease
    • Usami S, Takahashi K, Yuge I, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G: Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochlea-vestibular dysfunction, but not of Ménière's disease. Eur J Hum Genet 2003; 11: 744-748.
    • (2003) Eur J Hum Genet , vol.11 , pp. 744-748
    • Usami, S.1    Takahashi, K.2    Yuge, I.3    Ohtsuka, A.4    Namba, A.5    Abe, S.6    Fransen, E.7    Patthy, L.8    Otting, G.9    Van Camp, G.10
  • 31
    • 0026439315 scopus 로고
    • A new autosomal dominant syndrome of idiopathic progressive vestibulo-cochlear dysfunction with middle-age onset
    • Verhagen WI, Huygen PL, Bles W: A new autosomal dominant syndrome of idiopathic progressive vestibulo-cochlear dysfunction with middle-age onset. Acta Otolaryngol 1992; 112:899-906.
    • (1992) Acta Otolaryngol , vol.112 , pp. 899-906
    • Verhagen, W.I.1    Huygen, P.L.2    Bles, W.3
  • 33
    • 0023736070 scopus 로고
    • Type II collagen distribution in rodents
    • Yoo TJ, Tomoda K: Type II collagen distribution in rodents. Laryngoscope 1988; 98: 1255-1260.
    • (1988) Laryngoscope , vol.98 , pp. 1255-1260
    • Yoo, T.J.1    Tomoda, K.2
  • 34
    • 0021491565 scopus 로고
    • Antibody activity in perilymph from rats with type II collagen-induced autoimmune inner ear disease
    • Yoo TJ, Yazawa Y, Floyd R, Tomoda K: Antibody activity in perilymph from rats with type II collagen-induced autoimmune inner ear disease. Ann Otol Rhinol Laryngol Suppl 1984; 113:1-2.
    • (1984) Ann Otol Rhinol Laryngol Suppl , vol.113 , pp. 1-2
    • Yoo, T.J.1    Yazawa, Y.2    Floyd, R.3    Tomoda, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.