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Varitint-waddler: A double whammy for hearing
被引:10
作者
:
Steel, KP
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nottingham, MRC, Inst Hearing Res, Nottingham NG7 2RD, England
Univ Nottingham, MRC, Inst Hearing Res, Nottingham NG7 2RD, England
Steel, KP
[
1
]
机构
:
[1]
Univ Nottingham, MRC, Inst Hearing Res, Nottingham NG7 2RD, England
来源
:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
|
2002年
/ 99卷
/ 23期
关键词
:
D O I
:
10.1073/pnas.232585699
中图分类号
:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号
:
07 ;
0710 ;
09 ;
摘要
:
引用
收藏
页码:14613 / 14615
页数:3
相关论文
共 33 条
[1]
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
[J].
Alagramam, KN
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Alagramam, KN
;
Murcia, CL
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Murcia, CL
;
Kwon, HY
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Kwon, HY
;
Pawlowski, KS
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Pawlowski, KS
;
Wright, CG
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Wright, CG
;
Woychik, RP
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Woychik, RP
.
NATURE GENETICS,
2001,
27
(01)
:99
-102
[2]
Identification of the gene causing mucolipidosis type IV
[J].
Bargal, R
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Bargal, R
;
Avidan, N
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Avidan, N
;
Ben-Asher, E
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Ben-Asher, E
;
Olender, Z
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Olender, Z
;
Zeigler, M
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Zeigler, M
;
Frumkin, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Frumkin, A
;
Raas-Rothschild, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Raas-Rothschild, A
;
论文数:
引用数:
h-index:
机构:
Glusman, G
;
论文数:
引用数:
h-index:
机构:
Lancet, D
;
Bach, G
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Bach, G
.
NATURE GENETICS,
2000,
26
(01)
:118
-121
[3]
CHARACTERISTICS OF STRIA VASCULARIS MELANOCYTES OF VIABLE-DOMINANT SPOTTING (WV/WV) MOUSE MUTANTS
[J].
CABLE, J
论文数:
0
引用数:
0
h-index:
0
机构:
MRC Institute of Hearing Research, Nottingham, University Park
CABLE, J
;
BARKWAY, C
论文数:
0
引用数:
0
h-index:
0
机构:
MRC Institute of Hearing Research, Nottingham, University Park
BARKWAY, C
;
STEEL, KP
论文数:
0
引用数:
0
h-index:
0
机构:
MRC Institute of Hearing Research, Nottingham, University Park
STEEL, KP
.
HEARING RESEARCH,
1992,
64
(01)
:6
-20
[4]
MUTATIONS AT THE W-LOCUS AFFECT SURVIVAL OF NEURAL CREST-DERIVED MELANOCYTES IN THE MOUSE
[J].
CABLE, J
论文数:
0
引用数:
0
h-index:
0
机构:
MRC, INST HEARING RES, NOTTINGHAM NG7 2RD, ENGLAND
CABLE, J
;
JACKSON, IJ
论文数:
0
引用数:
0
h-index:
0
机构:
MRC, INST HEARING RES, NOTTINGHAM NG7 2RD, ENGLAND
JACKSON, IJ
;
STEEL, KP
论文数:
0
引用数:
0
h-index:
0
机构:
MRC, INST HEARING RES, NOTTINGHAM NG7 2RD, ENGLAND
STEEL, KP
.
MECHANISMS OF DEVELOPMENT,
1995,
50
(2-3)
:139
-150
[5]
Combined cochleo-saccular and neuroepithelial abnormalities in the Varitint-waddler-J (VaJ) mouse
[J].
Cable, J
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Biol Sci, Bristol BS8 1UG, Avon, England
Cable, J
;
Steel, KP
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Biol Sci, Bristol BS8 1UG, Avon, England
Steel, KP
.
HEARING RESEARCH,
1998,
123
(1-2)
:125
-136
[6]
THE VARITINT-WADDLER MOUSE - A DOMINANT MUTATION IN MUS-MUSCULUS
[J].
CLOUDMAN, AM
论文数:
0
引用数:
0
h-index:
0
CLOUDMAN, AM
;
BUNKER, LE
论文数:
0
引用数:
0
h-index:
0
BUNKER, LE
.
JOURNAL OF HEREDITY,
1945,
36
(09)
:258
-263
[7]
THE ANOMALIES OF THE LABYRINTH OF THE MUTANTS VARITINT-WADDLER, SHAKER-2 AND JERKER IN THE MOUSE
[J].
DEOL, MS
论文数:
0
引用数:
0
h-index:
0
DEOL, MS
.
JOURNAL OF GENETICS,
1954,
52
(03)
:562
-&
[8]
Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice
[J].
Di Palma, F
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Di Palma, F
;
Belyantseva, IA
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Belyantseva, IA
;
Kim, HJ
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Kim, HJ
;
Vogt, TF
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Vogt, TF
;
Kachar, B
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Kachar, B
;
Noben-Trauth, K
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Noben-Trauth, K
.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
2002,
99
(23)
:14994
-14999
[9]
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
[J].
Di Palma, F
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Di Palma, F
;
Holme, RH
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Holme, RH
;
Bryda, EC
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Bryda, EC
;
Belyantseva, IA
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Belyantseva, IA
;
Pellegrino, R
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Pellegrino, R
;
Kachar, B
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Kachar, B
;
Steel, KP
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Steel, KP
;
Noben-Trauth, K
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Noben-Trauth, K
.
NATURE GENETICS,
2001,
27
(01)
:103
-107
[10]
ERVEN A, 2002, IN PRESS EUR J NEURO
←
1
2
3
4
→
共 33 条
[1]
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
[J].
Alagramam, KN
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Alagramam, KN
;
Murcia, CL
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Murcia, CL
;
Kwon, HY
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Kwon, HY
;
Pawlowski, KS
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Pawlowski, KS
;
Wright, CG
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Wright, CG
;
Woychik, RP
论文数:
0
引用数:
0
h-index:
0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
Woychik, RP
.
NATURE GENETICS,
2001,
27
(01)
:99
-102
[2]
Identification of the gene causing mucolipidosis type IV
[J].
Bargal, R
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Bargal, R
;
Avidan, N
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Avidan, N
;
Ben-Asher, E
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Ben-Asher, E
;
Olender, Z
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Olender, Z
;
Zeigler, M
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Zeigler, M
;
Frumkin, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Frumkin, A
;
Raas-Rothschild, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Raas-Rothschild, A
;
论文数:
引用数:
h-index:
机构:
Glusman, G
;
论文数:
引用数:
h-index:
机构:
Lancet, D
;
Bach, G
论文数:
0
引用数:
0
h-index:
0
机构:
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Hadassah Hebrew Univ Hosp, Dept Human Genet, Jerusalem, Israel
Bach, G
.
NATURE GENETICS,
2000,
26
(01)
:118
-121
[3]
CHARACTERISTICS OF STRIA VASCULARIS MELANOCYTES OF VIABLE-DOMINANT SPOTTING (WV/WV) MOUSE MUTANTS
[J].
CABLE, J
论文数:
0
引用数:
0
h-index:
0
机构:
MRC Institute of Hearing Research, Nottingham, University Park
CABLE, J
;
BARKWAY, C
论文数:
0
引用数:
0
h-index:
0
机构:
MRC Institute of Hearing Research, Nottingham, University Park
BARKWAY, C
;
STEEL, KP
论文数:
0
引用数:
0
h-index:
0
机构:
MRC Institute of Hearing Research, Nottingham, University Park
STEEL, KP
.
HEARING RESEARCH,
1992,
64
(01)
:6
-20
[4]
MUTATIONS AT THE W-LOCUS AFFECT SURVIVAL OF NEURAL CREST-DERIVED MELANOCYTES IN THE MOUSE
[J].
CABLE, J
论文数:
0
引用数:
0
h-index:
0
机构:
MRC, INST HEARING RES, NOTTINGHAM NG7 2RD, ENGLAND
CABLE, J
;
JACKSON, IJ
论文数:
0
引用数:
0
h-index:
0
机构:
MRC, INST HEARING RES, NOTTINGHAM NG7 2RD, ENGLAND
JACKSON, IJ
;
STEEL, KP
论文数:
0
引用数:
0
h-index:
0
机构:
MRC, INST HEARING RES, NOTTINGHAM NG7 2RD, ENGLAND
STEEL, KP
.
MECHANISMS OF DEVELOPMENT,
1995,
50
(2-3)
:139
-150
[5]
Combined cochleo-saccular and neuroepithelial abnormalities in the Varitint-waddler-J (VaJ) mouse
[J].
Cable, J
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Biol Sci, Bristol BS8 1UG, Avon, England
Cable, J
;
Steel, KP
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Biol Sci, Bristol BS8 1UG, Avon, England
Steel, KP
.
HEARING RESEARCH,
1998,
123
(1-2)
:125
-136
[6]
THE VARITINT-WADDLER MOUSE - A DOMINANT MUTATION IN MUS-MUSCULUS
[J].
CLOUDMAN, AM
论文数:
0
引用数:
0
h-index:
0
CLOUDMAN, AM
;
BUNKER, LE
论文数:
0
引用数:
0
h-index:
0
BUNKER, LE
.
JOURNAL OF HEREDITY,
1945,
36
(09)
:258
-263
[7]
THE ANOMALIES OF THE LABYRINTH OF THE MUTANTS VARITINT-WADDLER, SHAKER-2 AND JERKER IN THE MOUSE
[J].
DEOL, MS
论文数:
0
引用数:
0
h-index:
0
DEOL, MS
.
JOURNAL OF GENETICS,
1954,
52
(03)
:562
-&
[8]
Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice
[J].
Di Palma, F
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Di Palma, F
;
Belyantseva, IA
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Belyantseva, IA
;
Kim, HJ
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Kim, HJ
;
Vogt, TF
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Vogt, TF
;
Kachar, B
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Kachar, B
;
Noben-Trauth, K
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Neurogenet Sect, Mol Biol Lab, NIH, Rockville, MD 20850 USA
Noben-Trauth, K
.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
2002,
99
(23)
:14994
-14999
[9]
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
[J].
Di Palma, F
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Di Palma, F
;
Holme, RH
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Holme, RH
;
Bryda, EC
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Bryda, EC
;
Belyantseva, IA
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Belyantseva, IA
;
Pellegrino, R
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Pellegrino, R
;
Kachar, B
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Kachar, B
;
Steel, KP
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Steel, KP
;
Noben-Trauth, K
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Natl Inst Deafness & Other Commun Disorders, Sect Murine Genet, Genet Mol Lab, NIH, Rockville, MD USA
Noben-Trauth, K
.
NATURE GENETICS,
2001,
27
(01)
:103
-107
[10]
ERVEN A, 2002, IN PRESS EUR J NEURO
←
1
2
3
4
→