-
1
-
-
0030989662
-
A molecular model for mechanosensation in Caenorhabditis elegans
-
(1997)
Biol. Bull.
, vol.192
, pp. 125-130
-
-
Chalfie, M.1
-
8
-
-
0024536382
-
Genetic control o f differentiation of the Caenorhabditis elegans touch receptor neurons
-
(1989)
Science
, vol.243
, pp. 1027-1033
-
-
Chalfie, M.1
Au, M.2
-
10
-
-
0024043341
-
mec-3, a homeobox-containing gene that specifies differentiation of the touch receptor neurons in C. elegans
-
(1988)
Cell
, vol.54
, pp. 5-16
-
-
Way, J.C.1
Chalfie, M.2
-
11
-
-
0024688962
-
mec-7 is a beta-tubulin gene required for the production of 15-protofilament microtubules in Caenorhabditis elegans
-
(1989)
Genes Dev.
, vol.3
, pp. 870-881
-
-
Savage, C.1
-
12
-
-
0033037583
-
MEC-12, an α-tubulin required for touch sensitivity in C. elegans
-
(1999)
J. Cell Sci.
, vol.112
, pp. 395-403
-
-
Fukushige, T.1
-
18
-
-
0028127759
-
Gene interactions affecting mechanosensory transduction in Caenorhabditis elegans
-
(1994)
Nature
, vol.367
, pp. 467-470
-
-
Huang, M.1
Chalfie, M.2
-
21
-
-
0031891297
-
Ripped pocket and pickpocket, novel Drosophila DEG/ENaC subunits expressed in early development and in mechanosensory neurons
-
(1998)
J. Cell Biol.
, vol.140
, pp. 143-152
-
-
Adams, C.M.1
-
24
-
-
0034718899
-
The mammalian sodium channel BNCl is required for normal touch sensation
-
(2000)
Nature
, vol.407
, pp. 1007-1011
-
-
Price, M.P.1
-
25
-
-
0034062889
-
+ channels and stomatin are expressed in rat trigeminal mechanosensory neurons
-
(2000)
Cell Tissue Res.
, vol.299
, pp. 327-334
-
-
Fricke, B.1
-
28
-
-
0028306979
-
Genetic dissection of mechanosensory transduction: Mechanoreception - Defective mutations of Drosophila
-
(1994)
Neuron
, vol.12
, pp. 1195-1206
-
-
Kernan, M.1
Cowan, D.2
Zuker, C.3
-
36
-
-
0034721648
-
Vanilloid receptor-related osmotically activated channel (VR-OAC), a candidate vertebrate osmoreceptor
-
(2000)
Cell
, vol.103
, pp. 525-535
-
-
Liedtke, W.1
-
38
-
-
0032427792
-
Cell fate choices and the expression of Notch, Delta and Serrate homologues in the chick inner ear: Parallels with Drosophila sense-organ development
-
(1998)
Development
, vol.125
, pp. 4646-4654
-
-
Adam, J.1
-
39
-
-
0033546004
-
Math 1: An essential gene for the generation of inner ear hair cells
-
(1999)
Science
, vol.284
, pp. 1837-1841
-
-
Bermingham, N.A.1
-
40
-
-
0034023488
-
Functional conservation of atonatal Math1 in the CNS and PNS
-
(2000)
Development
, vol.127
, pp. 1039-1048
-
-
Ben-Arie, N.1
-
47
-
-
0031984135
-
Calcium permeation of the turtle hair cell mechanotransducer channel and its relation to the composition of endolymph
-
(1998)
J. Physiol.
, vol.506
, pp. 159-173
-
-
Ricci, A.J.1
Fettiplace, R.2
-
50
-
-
0016696634
-
Effects of different ionic environments on the mechano-sensitivity of the lateral line organs in the mudpuppy
-
(1975)
J. Comp. Physiol. A
, vol.102
, pp. 27-42
-
-
Sand, O.1
-
54
-
-
0032899649
-
Mechano-electrical transduction in mice lacking the alpha-subunlt of the epithelial sodium channel
-
(1999)
Hear Res.
, vol.131
, pp. 170-176
-
-
Rusch, A.1
Hummler, E.2
-
55
-
-
18244431841
-
2 receptor subunit of the ATP-gated ion channel in the cochlea: Implications for sound transduction and auditory, neurotransmission
-
(1999)
J. Neurosci.
, vol.19
, pp. 8377-8388
-
-
Housley, G.D.1
-
56
-
-
0032550299
-
Localization of mRNA encoding the P2X2 receptor subunit of the adenosine 5′-triphosphate-gated ion channel in the adult and developing rat inner ear by in situ hybridization
-
(1998)
J. Comp. Neurol.
, vol.393
, pp. 403-414
-
-
Housley, G.D.1
Luo, L.2
Ryan, A.F.3
-
63
-
-
0031008059
-
The effects of calcium buffering and cyclic AMP on mechano-electrical transduction in turtle auditory hair cells
-
(1997)
J. Physiol.
, vol.501
, pp. 111-124
-
-
Ricci, A.J.1
Fettiplace, R.2
-
68
-
-
0032806387
-
A missense mutation in myosin VIIA prevents aminoglycoside accumulation in early postnatal cochlear hair cells
-
(1999)
Ann. NY Acad. Sci.
, vol.884
, pp. 110-124
-
-
Richardson, G.P.1
-
70
-
-
0028860302
-
A type VII myosin encoded by the mouse deafness gene shaker-1
-
(1995)
Nature
, vol.374
, pp. 62-64
-
-
Gibson, F.1
-
71
-
-
0031884319
-
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells
-
(1998)
Development
, vol.125
, pp. 557-566
-
-
Self, T.1
-
72
-
-
0034284683
-
Mariner is defective in myosin VIIA: A zebrafish model for human hereditary deafness
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2189-2196
-
-
Ernest, S.1
-
73
-
-
0030973305
-
Unconventional myosins in inner-ear sensory epithelia
-
(1997)
J. Cell Biol.
, vol.137
, pp. 1287-1307
-
-
Hasson, T.1
-
74
-
-
0035158639
-
Mutation of CDH23, encoding a new m ember of the cadherin gene family, causes Usher syndrome type 1D
-
(2001)
Nature Genet.
, vol.27
, pp. 108-112
-
-
Bolz, H.1
-
75
-
-
0035168151
-
Mutations in Cdh23, encoding a new type ofcadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
-
(2001)
Nature Genet.
, vol.27
, pp. 103-107
-
-
Di Palma, F.1
-
78
-
-
0035159856
-
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
-
(2001)
Nature Genet.
, vol.27
, pp. 99-102
-
-
Alagramam, K.N.1
-
79
-
-
0032511101
-
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type 11a
-
(1998)
Science
, vol.280
, pp. 1753-1757
-
-
Eudy, J.D.1
-
81
-
-
0034669042
-
Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex
-
(2000)
EMBO J.
, vol.19
, pp. 6020-6029
-
-
Kussel-Andermann, P.1
-
82
-
-
0033569707
-
Role of myosin V1 in the differentiation of cochlear hair cells
-
(1999)
Dev. Biol.
, vol.214
, pp. 331-341
-
-
Self, T.1
-
88
-
-
0035878074
-
2+-ATPase isoform 2a is the PMCA of hair bundles
-
(2001)
J. Neurosci.
, vol.21
, pp. 5066-5078
-
-
Dumont, R.1
-
95
-
-
0024460136
-
Preliminary biochemical characterization of the stereocilia and cuticular plate of hair cells of the chick cochlea
-
(1989)
J. Cell Biol.
, vol.109
, pp. 1711-1723
-
-
Tilney, M.S.1
-
96
-
-
0034604349
-
The deaf jerker mouse has a mutation in the gene encod ink the espin actin-bundling proteins of hair cell stereocilia and lacks espins
-
(2000)
Cell
, vol.102
, pp. 377-385
-
-
Zheng, L.1
-
97
-
-
0030707797
-
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous
-
(1997)
Science
, vol.278
, pp. 1313-1318
-
-
Lynch, E.D.1
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