메뉴 건너뛰기




Volumn 96, Issue 3, 1999, Pages 437-446

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; MEMBRANE PROTEIN KCNQ4; POTASSIUM CHANNEL; UNCLASSIFIED DRUG;

EID: 0033524936     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(00)80556-5     Document Type: Article
Times cited : (717)

References (43)
  • 1
    • 0029952101 scopus 로고    scopus 로고
    • K.LQT1 and IsK (minK) proteins associate to form the IKs cardiac potassium current
    • Barhanin, J., Lesage, F., Guillemare, E., Fink, M., Lazdunski, M., and Romey, G. (1996). K.LQT1 and IsK (minK) proteins associate to form the IKs cardiac potassium current. Nature 384, 78-80.
    • (1996) Nature , vol.384 , pp. 78-80
    • Barhanin, J.1    Lesage, F.2    Guillemare, E.3    Fink, M.4    Lazdunski, M.5    Romey, G.6
  • 3
    • 0031974209 scopus 로고    scopus 로고
    • A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
    • Charlier, C., Singh, N.A., Ryan, S.G., Lewis, T.B., Reus, B.E., Leach, R.J., and Leppert, M. (1998). A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nat. Genet. 18, 53-55.
    • (1998) Nat. Genet. , vol.18 , pp. 53-55
    • Charlier, C.1    Singh, N.A.2    Ryan, S.G.3    Lewis, T.B.4    Reus, B.E.5    Leach, R.J.6    Leppert, M.7
  • 8
    • 0013907716 scopus 로고
    • Pathology of the ear in the cardioauditory syndrome of Jervell and Lange-Nielsen (recessive deafness with electrocardiographic abnormalities)
    • Friedmann, l., Fraser, G.R., and Froggatt, P. (1966). Pathology of the ear in the cardioauditory syndrome of Jervell and Lange-Nielsen (recessive deafness with electrocardiographic abnormalities). J. Laryngol. Otol. 80, 451-470.
    • (1966) J. Laryngol. Otol. , vol.80 , pp. 451-470
    • Friedmann, L.1    Fraser, G.R.2    Froggatt, P.3
  • 10
    • 0026607661 scopus 로고
    • Ionic currents of outer hair cells isolated from the guinea-pig cochlea
    • Housley, G.D., and Ashmore, J.F. (1992). Ionic currents of outer hair cells isolated from the guinea-pig cochlea. J. Physiol. 448, 73-98.
    • (1992) J. Physiol. , vol.448 , pp. 73-98
    • Housley, G.D.1    Ashmore, J.F.2
  • 11
    • 0029781858 scopus 로고    scopus 로고
    • Effects of salicylate and lanthanides on outer hair cell motility and associated gating charge
    • Kakehata, S., and Santos-Sacchi, J. (1996). Effects of salicylate and lanthanides on outer hair cell motility and associated gating charge. J. Neurosci. 16, 4881-4889.
    • (1996) J. Neurosci. , vol.16 , pp. 4881-4889
    • Kakehata, S.1    Santos-Sacchi, J.2
  • 12
    • 0031683423 scopus 로고    scopus 로고
    • The fundamental and medical impacts of recent progress in research on hereditary hearing loss
    • Kalatzis, V., and Petit, C. (1998). The fundamental and medical impacts of recent progress in research on hereditary hearing loss. Hum. Mol. Genet. 7, 1589-1597.
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 1589-1597
    • Kalatzis, V.1    Petit, C.2
  • 14
    • 0028843286 scopus 로고
    • Gap junctions in the rat cochlea: Immunohistochemical and ultrastructural analysis
    • Kikuchi, T., Kimura, R.S., Paul, D.L., and Adams, J.C. (1995). Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis. Anat. Embryol. 797, 101-118.
    • (1995) Anat. Embryol. , vol.797 , pp. 101-118
    • Kikuchi, T.1    Kimura, R.S.2    Paul, D.L.3    Adams, J.C.4
  • 15
  • 16
    • 0029843417 scopus 로고    scopus 로고
    • Heteromultimeric CLC chloride channels with novel properties
    • Lorenz, C., Pusch, M., and Jentsch, T.J. (1996). Heteromultimeric CLC chloride channels with novel properties. Proc. Natl. Acad. Sci. USA 93, 13362-13366.
    • (1996) Proc. Natl. Acad. Sci. USA , vol.93 , pp. 13362-13366
    • Lorenz, C.1    Pusch, M.2    Jentsch, T.J.3
  • 17
    • 0029909037 scopus 로고    scopus 로고
    • Differential expression of outer hair cell potassium currents in the isolated cochlea of the guinea-pig
    • Mammano, F., and Ashmore, J.F. (1996). Differential expression of outer hair cell potassium currents in the isolated cochlea of the guinea-pig. J. Physiol. 496, 639-646.
    • (1996) J. Physiol. , vol.496 , pp. 639-646
    • Mammano, F.1    Ashmore, J.F.2
  • 18
    • 0031001337 scopus 로고    scopus 로고
    • Control of M-current
    • Marrion, N.V. (1997). Control of M-current. Annu. Rev. Physiol. 59, 483-504.
    • (1997) Annu. Rev. Physiol. , vol.59 , pp. 483-504
    • Marrion, N.V.1
  • 19
    • 0032977996 scopus 로고    scopus 로고
    • An α-tectorin gene defect causes a newly identified autosomal recessive form of sensineuronal prelingual deafness, DFNB21
    • in press
    • Mustapha, M., Weil, D., Chardenoux, S., Elias, S., El-Zir, E., Beckmann, J., Loiselet, J., and Petit, C. (1999). An α-tectorin gene defect causes a newly identified autosomal recessive form of sensineuronal prelingual deafness, DFNB21. Hum. Mol. Genet., in press.
    • (1999) Hum. Mol. Genet.
    • Mustapha, M.1    Weil, D.2    Chardenoux, S.3    Elias, S.4    El-Zir, E.5    Beckmann, J.6    Loiselet, J.7    Petit, C.8
  • 21
    • 0032055329 scopus 로고    scopus 로고
    • How well do we understand the cochlea?
    • Nobili, R., Mammano, F., and Ashmore, J. (1998). How well do we understand the cochlea? Trends Neurosci. 21, 159-167.
    • (1998) Trends Neurosci. , vol.21 , pp. 159-167
    • Nobili, R.1    Mammano, F.2    Ashmore, J.3
  • 22
    • 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
  • 23
    • 0029840732 scopus 로고    scopus 로고
    • KVLQT1 mutations in three families with familial or sporadic long QT syndrome
    • Russell, M.W., Dick, M., Collins, F.S., and Brody, L.C. (1996). KVLQT1 mutations in three families with familial or sporadic long QT syndrome. Hum. Mol. Genet. 5, 1319-1324.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1319-1324
    • Russell, M.W.1    Dick, M.2    Collins, F.S.3    Brody, L.C.4
  • 24
  • 26
    • 0027773169 scopus 로고
    • A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: In situ hybridization using digoxigenin-labelled cRNA probes
    • Schaeren-Wiemers, N., and Gerfin-Moser, A. (1993). A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes. Histochemistry 700, 431-440.
    • (1993) Histochemistry , vol.700 , pp. 431-440
    • Schaeren-Wiemers, N.1    Gerfin-Moser, A.2
  • 30
    • 0030271580 scopus 로고    scopus 로고
    • The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency
    • Spicer, S.S., and Schulte, B.A. (1996). The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency. Hear. Res. 700, 80-100.
    • (1996) Hear. Res. , vol.700 , pp. 80-100
    • Spicer, S.S.1    Schulte, B.A.2
  • 31
    • 0031900032 scopus 로고    scopus 로고
    • + recycling pathway from inner hair cells
    • + recycling pathway from inner hair cells. Hear. Res. 118, 1-12.
    • (1998) Hear. Res. , vol.118 , pp. 1-12
    • Spicer, S.S.1    Schulte, B.A.2
  • 33
    • 0023734276 scopus 로고
    • Cloning of a membrane protein that induces a slow voltage-gated potassium current
    • Takumi, T., Ohkubo, H., and Nakanishi, S. (1988). Cloning of a membrane protein that induces a slow voltage-gated potassium current. Science 242, 1042-1045.
    • (1988) Science , vol.242 , pp. 1042-1045
    • Takumi, T.1    Ohkubo, H.2    Nakanishi, S.3
  • 39
    • 0032483972 scopus 로고    scopus 로고
    • The KCNQ2 and KCNQ3 potassium channel subunits: Molecular correlates of the M-channel
    • Wang, H.S., Pan, Z., Shi, W., Brown, B.S., Wymore, R.S., Cohen, I.S., Dixon, J.R., and McKinnon, D. (1998b). The KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel. Science 282, 1890-1893.
    • (1998) Science , vol.282 , pp. 1890-1893
    • Wang, H.S.1    Pan, Z.2    Shi, W.3    Brown, B.S.4    Wymore, R.S.5    Cohen, I.S.6    Dixon, J.R.7    McKinnon, D.8
  • 40
    • 0030951102 scopus 로고    scopus 로고
    • The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
    • Well, D., Kussel, P., Blanchard, S., Levy, G., Levi-Acobas, F., Drira, M., Ayadi, H., and Petit, C. (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
    • Well, D.1    Kussel, P.2    Blanchard, S.3    Levy, G.4    Levi-Acobas, F.5    Drira, M.6    Ayadi, H.7    Petit, C.8
  • 41
    • 0021816489 scopus 로고
    • Deafness in developing countries. Approaches to a global program of prevention
    • Wilson, J. (1985). Deafness in developing countries. Approaches to a global program of prevention. Arch. Otolaryngol. 111, 2-9.
    • (1985) Arch. Otolaryngol. , vol.111 , pp. 2-9
    • Wilson, J.1
  • 42
    • 0030782276 scopus 로고    scopus 로고
    • Pathophysiological mechanisms of dominant and recessive KVLQT1 K channel mutations found in inherited cardiac arrhythmias
    • Wollnik, B., Schroeder, B.C., Kubisch, C., Esperer, H.D., Wieacker, P., and Jentsch, T.J. (1997). Pathophysiological mechanisms of dominant and recessive KVLQT1 K channel mutations found in inherited cardiac arrhythmias. Hum. Mol. Genet. 6, 1943-1949.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 1943-1949
    • Wollnik, B.1    Schroeder, B.C.2    Kubisch, C.3    Esperer, H.D.4    Wieacker, P.5    Jentsch, T.J.6
  • 43
    • 0032584595 scopus 로고    scopus 로고
    • Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy
    • Yang, W.P., Levesque, P.C., Little, W.A., Conder, M.L., Ramakrishnan, P., Neubauer, M.G., and Blanar, M.A. (1998). Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy. J. Biol. Chem. 273, 19419-19423.
    • (1998) J. Biol. Chem. , vol.273 , pp. 19419-19423
    • Yang, W.P.1    Levesque, P.C.2    Little, W.A.3    Conder, M.L.4    Ramakrishnan, P.5    Neubauer, M.G.6    Blanar, M.A.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.