共 54 条
Genes involved in deafness
被引:25
作者:

Holme, RH
论文数: 0 引用数: 0
h-index: 0
机构:
MRC, Inst Hearing Res, Nottingham NG7 2RD, England MRC, Inst Hearing Res, Nottingham NG7 2RD, England

Steel, KP
论文数: 0 引用数: 0
h-index: 0
机构:
MRC, Inst Hearing Res, Nottingham NG7 2RD, England MRC, Inst Hearing Res, Nottingham NG7 2RD, England
机构:
[1] MRC, Inst Hearing Res, Nottingham NG7 2RD, England
关键词:
D O I:
10.1016/S0959-437X(99)80046-X
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Remarkable progress has been made over the past few years in the field of hereditary deafness. To date, mutations in at least 35 genes are known to cause hearing loss. We are now beginning to understand the function of many of these genes, which affect diverse aspects of ear development and function.
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页码:309 / 314
页数:6
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共 54 条
[1]
A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
[J].
Abdelhak, S
;
Kalatzis, V
;
Heilig, R
;
Compain, S
;
Samson, D
;
Vincent, C
;
Weil, D
;
Cruaud, C
;
Sahly, I
;
Leibovici, M
;
BitnerGlindzicz, M
;
Francis, M
;
Lacombe, D
;
Vigneron, J
;
Charachon, R
;
Boven, K
;
Bedbeder, P
;
VanRegemorter, N
;
Weissenbach, J
;
Petit, C
.
NATURE GENETICS,
1997, 15 (02)
:157-164

Abdelhak, S
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Kalatzis, V
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Heilig, R
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Compain, S
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Samson, D
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Vincent, C
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Weil, D
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Cruaud, C
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Sahly, I
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Leibovici, M
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

BitnerGlindzicz, M
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Francis, M
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Lacombe, D
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Vigneron, J
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Charachon, R
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Boven, K
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Bedbeder, P
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

VanRegemorter, N
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Weissenbach, J
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE

Petit, C
论文数: 0 引用数: 0
h-index: 0
机构: INST PASTEUR, URA CNRS 1968, UNITE GENET MOL HUMAINE, F-75724 PARIS 15, FRANCE
[2]
THE MOUSE SNELLS WALTZER DEAFNESS GENE ENCODES AN UNCONVENTIONAL MYOSIN REQUIRED FOR STRUCTURAL INTEGRITY OF INNER-EAR HAIR-CELLS
[J].
AVRAHAM, KB
;
HASSON, T
;
STEEL, KP
;
KINGSLEY, DM
;
RUSSELL, LB
;
MOOSEKER, MS
;
COPELAND, NG
;
JENKINS, NA
.
NATURE GENETICS,
1995, 11 (04)
:369-375

AVRAHAM, KB
论文数: 0 引用数: 0
h-index: 0
机构: YALE UNIV,DEPT CELL BIOL,NEW HAVEN,CT 06511

论文数: 引用数:
h-index:
机构:

STEEL, KP
论文数: 0 引用数: 0
h-index: 0
机构: YALE UNIV,DEPT CELL BIOL,NEW HAVEN,CT 06511

KINGSLEY, DM
论文数: 0 引用数: 0
h-index: 0
机构: YALE UNIV,DEPT CELL BIOL,NEW HAVEN,CT 06511

RUSSELL, LB
论文数: 0 引用数: 0
h-index: 0
机构: YALE UNIV,DEPT CELL BIOL,NEW HAVEN,CT 06511

MOOSEKER, MS
论文数: 0 引用数: 0
h-index: 0
机构: YALE UNIV,DEPT CELL BIOL,NEW HAVEN,CT 06511

COPELAND, NG
论文数: 0 引用数: 0
h-index: 0
机构: YALE UNIV,DEPT CELL BIOL,NEW HAVEN,CT 06511

JENKINS, NA
论文数: 0 引用数: 0
h-index: 0
机构: YALE UNIV,DEPT CELL BIOL,NEW HAVEN,CT 06511
[3]
AN EXONIC MUTATION IN THE HUP2 PAIRED DOMAIN GENE CAUSES WAARDENBURG SYNDROME
[J].
BALDWIN, CT
;
HOTH, CF
;
AMOS, JA
;
DASILVA, EO
;
MILUNSKY, A
.
NATURE,
1992, 355 (6361)
:637-638

BALDWIN, CT
论文数: 0 引用数: 0
h-index: 0
机构: BOSTON UNIV, SCH MED, CTR HUMAN GENET, 80 E CONCORD ST, BOSTON, MA 02118 USA

HOTH, CF
论文数: 0 引用数: 0
h-index: 0
机构: BOSTON UNIV, SCH MED, CTR HUMAN GENET, 80 E CONCORD ST, BOSTON, MA 02118 USA

AMOS, JA
论文数: 0 引用数: 0
h-index: 0
机构: BOSTON UNIV, SCH MED, CTR HUMAN GENET, 80 E CONCORD ST, BOSTON, MA 02118 USA

DASILVA, EO
论文数: 0 引用数: 0
h-index: 0
机构: BOSTON UNIV, SCH MED, CTR HUMAN GENET, 80 E CONCORD ST, BOSTON, MA 02118 USA

MILUNSKY, A
论文数: 0 引用数: 0
h-index: 0
机构: BOSTON UNIV, SCH MED, CTR HUMAN GENET, 80 E CONCORD ST, BOSTON, MA 02118 USA
[4]
INTERACTION OF ENDOTHELIN-3 WITH ENDOTHELIN-B RECEPTOR IS ESSENTIAL FOR DEVELOPMENT OF EPIDERMAL MELANOCYTES AND ENTERIC NEURONS
[J].
BAYNASH, AG
;
HOSODA, K
;
GIAID, A
;
RICHARDSON, JA
;
EMOTO, N
;
HAMMER, RE
;
YANAGISAWA, M
.
CELL,
1994, 79 (07)
:1277-1285

BAYNASH, AG
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SW MED CTR,DEPT MOLEC GENET,DALLAS,TX 75235

HOSODA, K
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SW MED CTR,DEPT MOLEC GENET,DALLAS,TX 75235

GIAID, A
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SW MED CTR,DEPT MOLEC GENET,DALLAS,TX 75235

RICHARDSON, JA
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SW MED CTR,DEPT MOLEC GENET,DALLAS,TX 75235

EMOTO, N
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SW MED CTR,DEPT MOLEC GENET,DALLAS,TX 75235

HAMMER, RE
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SW MED CTR,DEPT MOLEC GENET,DALLAS,TX 75235

YANAGISAWA, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV TEXAS,SW MED CTR,DEPT MOLEC GENET,DALLAS,TX 75235
[5]
Connexin 26 gene linked to a dominant deafness
[J].
Denoyelle, F
;
Lina-Granade, G
;
Plauchu, H
;
Bruzzone, R
;
Chaïb, H
;
Lévi-Acobas, F
;
Weil, D
;
Petit, C
.
NATURE,
1998, 393 (6683)
:319-320

Denoyelle, F
论文数: 0 引用数: 0
h-index: 0
机构: Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France

Lina-Granade, G
论文数: 0 引用数: 0
h-index: 0
机构: Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France

Plauchu, H
论文数: 0 引用数: 0
h-index: 0
机构: Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France

Bruzzone, R
论文数: 0 引用数: 0
h-index: 0
机构: Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France

Chaïb, H
论文数: 0 引用数: 0
h-index: 0
机构: Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France

Lévi-Acobas, F
论文数: 0 引用数: 0
h-index: 0
机构: Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France

Weil, D
论文数: 0 引用数: 0
h-index: 0
机构: Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France

Petit, C
论文数: 0 引用数: 0
h-index: 0
机构: Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France
[6]
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
[J].
Edery, P
;
Attie, T
;
Amiel, J
;
Pelet, A
;
Eng, C
;
Hofstra, RMW
;
Martelli, H
;
Bidaud, C
;
Munnich, A
;
Lyonnet, S
.
NATURE GENETICS,
1996, 12 (04)
:442-444

Edery, P
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Attie, T
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Amiel, J
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Pelet, A
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Eng, C
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Hofstra, RMW
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Martelli, H
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Bidaud, C
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Munnich, A
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE

Lyonnet, S
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INST NECKER,INSERM,U393,SERV GENET MED,F-75743 PARIS,FRANCE
[7]
Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development
[J].
Erkman, L
;
McEvilly, RJ
;
Luo, L
;
Ryan, AK
;
Hooshmand, F
;
OConnell, SM
;
Keithley, EM
;
Rapaport, DH
;
Ryan, AF
;
Rosenfeld, MG
.
NATURE,
1996, 381 (6583)
:603-606

Erkman, L
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

McEvilly, RJ
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

Luo, L
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

Ryan, AK
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

Hooshmand, F
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

OConnell, SM
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

Keithley, EM
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

Rapaport, DH
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

Ryan, AF
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA

Rosenfeld, MG
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, DEPT MED, LA JOLLA, CA 92093 USA
[8]
Development of the vertebrate ear: insights from knockouts and mutants
[J].
Fekete, DM
.
TRENDS IN NEUROSCIENCES,
1999, 22 (06)
:263-269

Fekete, DM
论文数: 0 引用数: 0
h-index: 0
机构:
Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[9]
A TYPE-VII MYOSIN ENCODED BY THE MOUSE DEAFNESS GENE SHAKER-1
[J].
GIBSON, F
;
WALSH, J
;
MBURU, P
;
VARELA, A
;
BROWN, KA
;
ANTONIO, M
;
BEISEL, KW
;
STEEL, KP
;
BROWN, SDM
.
NATURE,
1995, 374 (6517)
:62-64

GIBSON, F
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND

WALSH, J
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND

MBURU, P
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND

VARELA, A
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND

BROWN, KA
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND

ANTONIO, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND

BEISEL, KW
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND

STEEL, KP
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND

BROWN, SDM
论文数: 0 引用数: 0
h-index: 0
机构: UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED, ST MARYS HOSP, SCH MED, DEPT BIOCHEM & MOLEC GENET, LONDON W2 1PG, ENGLAND
[10]
Myosin and adaptation by hair cells
[J].
Gillespie, PG
;
Corey, DP
.
NEURON,
1997, 19 (05)
:955-958

Gillespie, PG
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV,DEPT NEUROSCI,BALTIMORE,MD 21205

Corey, DP
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV,DEPT NEUROSCI,BALTIMORE,MD 21205