-
1
-
-
0035775666
-
Usher syndrome: From genetics to pathogenesis
-
Petit, C. (2001) Usher syndrome: from genetics to pathogenesis. Annu. Rev. Genom. Hum. Genet., 2, 271-297.
-
(2001)
Annu. Rev. Genom. Hum. Genet.
, vol.2
, pp. 271-297
-
-
Petit, C.1
-
2
-
-
0028815440
-
Defective myosin VIIA gene responsible for Usher syndrome type 1B
-
Weil, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M.D, et al. (1995) Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature, 374, 60-61.
-
(1995)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
Blanchard, S.2
Kaplan, J.3
Guilford, P.4
Gibson, F.5
Walsh, J.6
Mburu, P.7
Varela, A.8
Levilliers, J.9
Weston, M.D.10
-
3
-
-
0033822063
-
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
-
Bitner-Glindzicz, M., Lindley, K.J., Rutland, P., Blaydon, D., Smith, V.V., Milla, P.J., Hussain, K., Furth-Lavi, J., Cosgrove, K.E., Shepherd, R.M. et al. (2000) A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene. Nat. Genet., 26, 56-60.
-
(2000)
Nat. Genet.
, vol.26
, pp. 56-60
-
-
Bitner-Glindzicz, M.1
Lindley, K.J.2
Rutland, P.3
Blaydon, D.4
Smith, V.V.5
Milla, P.J.6
Hussain, K.7
Furth-Lavi, J.8
Cosgrove, K.E.9
Shepherd, R.M.10
-
4
-
-
0033816925
-
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
-
Verpy, E., Leibovici, M., Zwaenepoel, I., Liu, X.-Z., Gal, A., Salem, N., Mansour, A., Blanchard, S., Kobayashi, I., Keats, B.J.B. et al. (2000) A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nat. Genet., 26, 51-55.
-
(2000)
Nat. Genet.
, vol.26
, pp. 51-55
-
-
Verpy, E.1
Leibovici, M.2
Zwaenepoel, I.3
Liu, X.-Z.4
Gal, A.5
Salem, N.6
Mansour, A.7
Blanchard, S.8
Kobayashi, I.9
Keats, B.J.B.10
-
5
-
-
0035158639
-
Mutations of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
-
Bolz, H., von Brederlow, B., Ramirez, A., Bryda, E.C., Kutsche, K., Nothwang, H.G., Seeliger, M., Salcedo Cabrera, M.d.C., Vila, M.C., Molina, O.P. et al. (2001) Mutations of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nat. Genet., 27, 108-112.
-
(2001)
Nat. Genet.
, vol.27
, pp. 108-112
-
-
Bolz, H.1
von Brederlow, B.2
Ramirez, A.3
Bryda, E.C.4
Kutsche, K.5
Nothwang, H.G.6
Seeliger, M.7
Salcedo Cabrera, M.D.C.8
Vila, M.C.9
Molina, O.P.10
-
6
-
-
0035168168
-
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
-
Bork, J.M., Peters, L.M., Riazuddin, S., Bernstein, S.L., Ahmed, Z.M., Ness, S.L., Polomeno, R., Ramesh, A., Schloss, M., Srisailpathy, C.R.S. et al. (2001) Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am. J. Hum. Genet. 68, 26-37.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 26-37
-
-
Bork, J.M.1
Peters, L.M.2
Riazuddin, S.3
Bernstein, S.L.4
Ahmed, Z.M.5
Ness, S.L.6
Polomeno, R.7
Ramesh, A.8
Schloss, M.9
Srisailpathy, C.R.S.10
-
7
-
-
0034968358
-
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
-
Ahmed, Z.M., Riazuddin, S., Bernstein, S.L., Ahmed, Z., Khan, S., Griffith, A.J., Morell, R.J., Friedman, T.B., Riazuddin, S. and Wilcox, E.R. (2001) Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am. J. Hum. Genet., 69, 25-34.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 25-34
-
-
Ahmed, Z.M.1
Riazuddin, S.2
Bernstein, S.L.3
Ahmed, Z.4
Khan, S.5
Griffith, A.J.6
Morell, R.J.7
Friedman, T.B.8
Riazuddin, S.9
Wilcox, E.R.10
-
8
-
-
0035421436
-
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
-
Alagramam, K.N., Yuan, H., Kuehn, M.H., Murcia, C.L., Wayne, S., Srisailpathy, C.R.S., Lowry, R.B., Knaus, R., Van Laer, L., Bernier, F.P. et al. (2001) Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. Hum. Mol. Genet., 10, 1709-1718.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1709-1718
-
-
Alagramam, K.N.1
Yuan, H.2
Kuehn, M.H.3
Murcia, C.L.4
Wayne, S.5
Srisailpathy, C.R.S.6
Lowry, R.B.7
Knaus, R.8
Van Laer, L.9
Bernier, F.P.10
-
9
-
-
0037341463
-
Usher syndrome type IG (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin
-
Weil, D., El-Amraoui, A., Masmoudi, S., Mustapha, M., Kikkawa, Y., Lainé, S., Delmaghani, S., Adato, A., Nadifi, S., Ben Zina, Z. et al. (2003) Usher syndrome type IG (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin. Hum. Mol. Genet., 12, 463-471.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 463-471
-
-
Weil, D.1
El-Amraoui, A.2
Masmoudi, S.3
Mustapha, M.4
Kikkawa, Y.5
Lainé, S.6
Delmaghani, S.7
Adato, A.8
Nadifi, S.9
Ben Zina, Z.10
-
10
-
-
0028860302
-
A type VII myosin encoded by the mouse deafness gene Shaker-1
-
Gibson, F., Walsh, J., Mburu, P., Varela, A., Brown, K.A., Antonio, M., Beisel, K.W., Steel, K.P. and Brown, S.D.M. (1995) A type VII myosin encoded by the mouse deafness gene Shaker-1. Nature, 374, 62-64.
-
(1995)
Nature
, vol.374
, pp. 62-64
-
-
Gibson, F.1
Walsh, J.2
Mburu, P.3
Varela, A.4
Brown, K.A.5
Antonio, M.6
Beisel, K.W.7
Steel, K.P.8
Brown, S.D.M.9
-
11
-
-
0345530996
-
Mouse models of USH1C and DFNB18: Phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene
-
Johnson, K.R., Gagnon, L.H., Webb, L.S., Peters, L.L., Hawes, N.L., Chang, B. and Zheng, Q.Y. (2003) Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene. Hum. Mol. Genet., 12, 3075-3086.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 3075-3086
-
-
Johnson, K.R.1
Gagnon, L.H.2
Webb, L.S.3
Peters, L.L.4
Hawes, N.L.5
Chang, B.6
Zheng, Q.Y.7
-
12
-
-
0035168151
-
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
-
Di Palma, F., Holme, R.H., Bryda, E.C., Belyantseva, I.A., Pellegrino, R., Kachar, B., Steel, K.P. and Noben-Trauth, K. (2001) Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nat. Genet., 27, 103-107.
-
(2001)
Nat. Genet.
, vol.27
, pp. 103-107
-
-
Di Palma, F.1
Holme, R.H.2
Bryda, E.C.3
Belyantseva, I.A.4
Pellegrino, R.5
Kachar, B.6
Steel, K.P.7
Noben-Trauth, K.8
-
13
-
-
0035366320
-
Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice
-
Wilson, S.M., Householder, D.B., Coppola, V., Tessarollo, L., Fritzsch, B., Lee, E.C., Goss, D., Carlson, G.A., Copeland, N.G. and Jenkins, N.A. (2001) Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice. Genomics, 74, 228-233.
-
(2001)
Genomics
, vol.74
, pp. 228-233
-
-
Wilson, S.M.1
Householder, D.B.2
Coppola, V.3
Tessarollo, L.4
Fritzsch, B.5
Lee, E.C.6
Goss, D.7
Carlson, G.A.8
Copeland, N.G.9
Jenkins, N.A.10
-
14
-
-
0035159856
-
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
-
Alagramam, K.N., Murcia, C.L., Kwon, H.Y., Pawlowski, K.S., Wright, C.G. and Woychik, R.P. (2001) The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene. Nat. Genet., 27, 99-102.
-
(2001)
Nat. Genet.
, vol.27
, pp. 99-102
-
-
Alagramam, K.N.1
Murcia, C.L.2
Kwon, H.Y.3
Pawlowski, K.S.4
Wright, C.G.5
Woychik, R.P.6
-
15
-
-
0037337023
-
Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice
-
Kikkawa, Y., Shitara, H., Wakana, S., Kohara, Y., Takada, T., Okamoto, M., Taya, C., Kamiya, K., Yoshikawa, Y., Tokano, H. et al. (2003) Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice. Hum. Mol. Genet., 12, 453-4561.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 453-4561
-
-
Kikkawa, Y.1
Shitara, H.2
Wakana, S.3
Kohara, Y.4
Takada, T.5
Okamoto, M.6
Taya, C.7
Kamiya, K.8
Yoshikawa, Y.9
Tokano, H.10
-
16
-
-
0031431389
-
Mechanical amplification of stimuli by hair cells
-
Hudspeth, A.J. (1997) Mechanical amplification of stimuli by hair cells. Curr. Opin. Neurobiol., 7, 480-486.
-
(1997)
Curr. Opin. Neurobiol.
, vol.7
, pp. 480-486
-
-
Hudspeth, A.J.1
-
17
-
-
12244277402
-
Myosin VIIa, harmonin, and cadherin 23, three Usher I gene products, cooperate to shape the sensory hair cell bundle
-
Boëda, B., El-Amraoui, A., Bahloul, A., Goodyear, R., Daviet, L., Blanchard, S., Perfettini, I., Fath, K.R., Shorte, S., Reiners, J. et al. (2002) Myosin VIIa, harmonin, and cadherin 23, three Usher I gene products, cooperate to shape the sensory hair cell bundle. EMBO J., 21, 6689-6699.
-
(2002)
EMBO J.
, vol.21
, pp. 6689-6699
-
-
Boëda, B.1
El-Amraoui, A.2
Bahloul, A.3
Goodyear, R.4
Daviet, L.5
Blanchard, S.6
Perfettini, I.7
Fath, K.R.8
Shorte, S.9
Reiners, J.10
-
18
-
-
0037069346
-
The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions
-
Siemens, J., Kazmierczak, P., Reynolds, A., Sticker, M., Littlewood-Evans, A. and Muller, U. (2002) The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions. Proc. Natl Acad. Sci. USA, 99, 14946-14951.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 14946-14951
-
-
Siemens, J.1
Kazmierczak, P.2
Reynolds, A.3
Sticker, M.4
Littlewood-Evans, A.5
Muller, U.6
-
19
-
-
0348013128
-
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
-
Ahmed, Z.M., Riazuddin, S., Ahmad, J., Bernstein, S.L., Guo, Y., Sabar, M.F., Sieving, P., Riazuddin, S., Griffith, A.J., Friedman, T.B. et al. (2003) PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Hum. Mol. Genet., 12, 3215-3223.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 3215-3223
-
-
Ahmed, Z.M.1
Riazuddin, S.2
Ahmad, J.3
Bernstein, S.L.4
Guo, Y.5
Sabar, M.F.6
Sieving, P.7
Riazuddin, S.8
Griffith, A.J.9
Friedman, T.B.10
-
20
-
-
0043168114
-
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with mutations in DFNB31
-
Mburu, P., Mustapha, M., Varela, A., Weil, D., El-Amraoui, A., Holme, R.H., Rump, A., Hardisty, R.E., Blanchard, S., Coimbra, R.S. et al. (2003) Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with mutations in DFNB31. Nat. Genet., 34, 421-428.
-
(2003)
Nat. Genet.
, vol.34
, pp. 421-428
-
-
Mburu, P.1
Mustapha, M.2
Varela, A.3
Weil, D.4
El-Amraoui, A.5
Holme, R.H.6
Rump, A.7
Hardisty, R.E.8
Blanchard, S.9
Coimbra, R.S.10
-
21
-
-
13544251711
-
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly
-
Delprat, B., Michel, V., Goodyear, R., Yamasaki, Y., Michalski, N., El-Amraoui, A., Perfettini, I., Legrain, P., Richardson, G., Hardelin, J.-P. and Petit, C. (2005) Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly. Hum. Mol. Genet., 14 401-410.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 401-410
-
-
Delprat, B.1
Michel, V.2
Goodyear, R.3
Yamasaki, Y.4
Michalski, N.5
El-Amraoui, A.6
Perfettini, I.7
Legrain, P.8
Richardson, G.9
Hardelin, J.-P.10
Petit, C.11
-
22
-
-
0031022602
-
SAM as a protein interaction domain involved in developmental regulation
-
Schultz, J., Ponting, C.P., Hofmann, K. and Bork, P. (1997) SAM as a protein interaction domain involved in developmental regulation. Protein Sci., 6, 249-253.
-
(1997)
Protein Sci.
, vol.6
, pp. 249-253
-
-
Schultz, J.1
Ponting, C.P.2
Hofmann, K.3
Bork, P.4
-
23
-
-
0032948019
-
The crystal structure of an Eph receptor SAM domain reveals a mechanism for modular dimerization
-
Stapleton, D., Balan, I., Pawson, T. and Sicheri, F. (1999) The crystal structure of an Eph receptor SAM domain reveals a mechanism for modular dimerization. Nat. Struct. Biol., 6, 44-49.
-
(1999)
Nat. Struct. Biol.
, vol.6
, pp. 44-49
-
-
Stapleton, D.1
Balan, I.2
Pawson, T.3
Sicheri, F.4
-
24
-
-
0032565762
-
Timed markers for the differentiation of the cuticular plate and stereocilia in hair cells from the mouse inner ear
-
Nishida, Y., Rivolta, M.N. and Holley, M.C. (1998) Timed markers for the differentiation of the cuticular plate and stereocilia in hair cells from the mouse inner ear. J. Comp. Neurol., 395, 18-28.
-
(1998)
J. Comp. Neurol.
, vol.395
, pp. 18-28
-
-
Nishida, Y.1
Rivolta, M.N.2
Holley, M.C.3
-
25
-
-
0033306252
-
Establishment of hair bundle polarity and orientation in the developing vestibular system of the mouse
-
Denman-Johnson, K. and Forge, A. (1999) Establishment of hair bundle polarity and orientation in the developing vestibular system of the mouse. J. Neurocytol., 28, 821-835.
-
(1999)
J. Neurocytol.
, vol.28
, pp. 821-835
-
-
Denman-Johnson, K.1
Forge, A.2
-
26
-
-
0031000463
-
Compartmentalized vesicular traffic around the hair cell cuticular plate
-
Kachar, B., Battaglia, A. and Fex, J. (1997) Compartmentalized vesicular traffic around the hair cell cuticular plate. Hear Res., 107, 102-112.
-
(1997)
Hear Res.
, vol.107
, pp. 102-112
-
-
Kachar, B.1
Battaglia, A.2
Fex, J.3
-
27
-
-
0026658957
-
Ultrastructural findings in the inner ear of Jackson shaker mice
-
Kitamura, K., Kakoi, H., Yoshikawa, Y. and Ochikubo, F. (1992) Ultrastructural findings in the inner ear of Jackson shaker mice. Acta Otolaryngol. (Stockh.), 112, 622-627.
-
(1992)
Acta Otolaryngol. (Stockh.)
, vol.112
, pp. 622-627
-
-
Kitamura, K.1
Kakoi, H.2
Yoshikawa, Y.3
Ochikubo, F.4
-
28
-
-
0030973305
-
Unconventional myosins in inner-ear sensory epithelia
-
Hasson, T., Gillespie, P.G., Garcia, J.A., MacDonald, R.B., Zhao, Y., Yee, A.G., Mooseker, M.S. and Corey, D.P. (1997) Unconventional myosins in inner-ear sensory epithelia. J. Cell Biol., 137, 1287-1307.
-
(1997)
J. Cell Biol.
, vol.137
, pp. 1287-1307
-
-
Hasson, T.1
Gillespie, P.G.2
Garcia, J.A.3
MacDonald, R.B.4
Zhao, Y.5
Yee, A.G.6
Mooseker, M.S.7
Corey, D.P.8
-
29
-
-
0032792551
-
The ankyrin repeat: A diversity of interactions on a common structural framework
-
Sedgwick, S.G. and Smerdon, S.J. (1999) The ankyrin repeat: a diversity of interactions on a common structural framework. Trends Biochem. Sci., 24, 311-316.
-
(1999)
Trends Biochem. Sci.
, vol.24
, pp. 311-316
-
-
Sedgwick, S.G.1
Smerdon, S.J.2
-
30
-
-
0036315303
-
Ankyrins, multifunctional proteins involved in many cellular pathways
-
Hryniewicz-Jankowska, A., Czogalla, A., Bok, E. and Sikorsk, A.F. (2002) Ankyrins, multifunctional proteins involved in many cellular pathways. Folia Histochem. Cytobiol., 40, 239-249.
-
(2002)
Folia Histochem. Cytobiol.
, vol.40
, pp. 239-249
-
-
Hryniewicz-Jankowska, A.1
Czogalla, A.2
Bok, E.3
Sikorsk, A.F.4
-
31
-
-
0029091904
-
SAM: A novel motif in yeast sterile and Drosophila polyhomeotic proteins
-
Ponting, C.P. (1995) SAM: a novel motif in yeast sterile and Drosophila polyhomeotic proteins. Protein Sci., 4, 1928-1930.
-
(1995)
Protein Sci.
, vol.4
, pp. 1928-1930
-
-
Ponting, C.P.1
-
32
-
-
0031938082
-
The SAM domain of polyhomeotic, RAE28, and scm mediates specific interactions through conserved residues
-
Kyba, M. and Brock, H.W. (1998) The SAM domain of polyhomeotic, RAE28, and scm mediates specific interactions through conserved residues. Dev. Genet., 22, 74-84.
-
(1998)
Dev. Genet.
, vol.22
, pp. 74-84
-
-
Kyba, M.1
Brock, H.W.2
-
33
-
-
0036289460
-
PIP(2)-PDZ domain binding controls the association of syntenin with the plasma membrane
-
Zimmermann, P., Meerschaert, K., Reekmans, G., Leenaerts, I., Small, J.V., Vandekerckhove, J., David, G. and Gettemans, J. (2002) PIP(2)-PDZ domain binding controls the association of syntenin with the plasma membrane. Mol. Cell, 9, 1215-1225.
-
(2002)
Mol. Cell
, vol.9
, pp. 1215-1225
-
-
Zimmermann, P.1
Meerschaert, K.2
Reekmans, G.3
Leenaerts, I.4
Small, J.V.5
Vandekerckhove, J.6
David, G.7
Gettemans, J.8
-
34
-
-
0012927828
-
PDZ domain proteins: Plug and play!
-
Nourry, C., Grant, S.G. and Borg, J.P. (2003) PDZ domain proteins: plug and play! Sci STKE, 2003, RE7.
-
(2003)
Sci. STKE
, vol.2003
-
-
Nourry, C.1
Grant, S.G.2
Borg, J.P.3
-
35
-
-
0029664550
-
2+ channel by INAD in Drosophila photoreceptors
-
2+ channel by INAD in Drosophila photoreceptors. Neuron, 16 991-998.
-
(1996)
Neuron
, vol.16
, pp. 991-998
-
-
Shieh, B.H.1
Zhu, M.Y.2
-
36
-
-
0142200818
-
Differential distribution of harmonin isoforms and their possible role in Usher-1 protein complexes in mammalian photoreceptor cells
-
Reiners, J., Reidel, B., El-Amraoui, A., Boëda, B., Huber, I., Petit, C. and Wolfrum, U. (2003) Differential distribution of harmonin isoforms and their possible role in Usher-1 protein complexes in mammalian photoreceptor cells. Invest. Ophthalmol. Visual Sci., 44, 5006-5015.
-
(2003)
Invest. Ophthalmol. Visual Sci.
, vol.44
, pp. 5006-5015
-
-
Reiners, J.1
Reidel, B.2
El-Amraoui, A.3
Boëda, B.4
Huber, I.5
Petit, C.6
Wolfrum, U.7
-
37
-
-
2342421512
-
Cadherin 23 is a component of the tip link in hair-cell stereocilia
-
Siemens, J., Lillo, C., Dumont, R.A., Reynolds, A., Williams, D.S., Gillespie, P.G., Muller, U. (2004) Cadherin 23 is a component of the tip link in hair-cell stereocilia. Nature, 428, 950-955.
-
(2004)
Nature
, vol.428
, pp. 950-955
-
-
Siemens, J.1
Lillo, C.2
Dumont, R.A.3
Reynolds, A.4
Williams, D.S.5
Gillespie, P.G.6
Muller, U.7
-
38
-
-
84905556082
-
Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells
-
Söllner, C., Rauch, G.-J., Siemens, J., Geisler, R., Schuster, S.C., Müller, U. and Nicolson, T. (2004) Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells. Nature, 428, 955-959.
-
(2004)
Nature
, vol.428
, pp. 955-959
-
-
Söllner, C.1
Rauch, G.-J.2
Siemens, J.3
Geisler, R.4
Schuster, S.C.5
Müller, U.6
Nicolson, T.7
-
39
-
-
0031884319
-
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells
-
Self, T., Mahony, M., Fleming, J., Walsh, J., Brown, S.D. and Steel, K.P. (1998) Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. Development, 125, 557-566.
-
(1998)
Development
, vol.125
, pp. 557-566
-
-
Self, T.1
Mahony, M.2
Fleming, J.3
Walsh, J.4
Brown, S.D.5
Steel, K.P.6
-
40
-
-
0035984893
-
MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes
-
El-Amraoui, A., Schonn, J.-S., Küssel-Andermann, P., Blanchard, S., Desnos, C., Henry, J.-P., Wolfrum, U., Darchen, F. and Petit, C. (2002) MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes. EMBO Rep., 3, 463-470.
-
(2002)
EMBO Rep.
, vol.3
, pp. 463-470
-
-
El-Amraoui, A.1
Schonn, J.-S.2
Küssel-Andermann, P.3
Blanchard, S.4
Desnos, C.5
Henry, J.-P.6
Wolfrum, U.7
Darchen, F.8
Petit, C.9
-
41
-
-
0036134043
-
Screening for protein-protein interactions in the yeast two-hybrid system
-
Gietz, R.D. and Woods, R.A. (2002) Screening for protein-protein interactions in the yeast two-hybrid system. Methods Mol. Biol., 185, 471-486.
-
(2002)
Methods Mol. Biol.
, vol.185
, pp. 471-486
-
-
Gietz, R.D.1
Woods, R.A.2
-
42
-
-
0034669042
-
Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex
-
Küssel-Andermann, P., El-Amraoui, A., Safieddine, S., Nouaille, S., Perfettini, I., Lecuit, M., Cossart, P., Wolfrum, U. and Petit, C. (2000) Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex. EMBO J., 19, 6020-6029.
-
(2000)
EMBO J.
, vol.19
, pp. 6020-6029
-
-
Küssel-Andermann, P.1
El-Amraoui, A.2
Safieddine, S.3
Nouaille, S.4
Perfettini, I.5
Lecuit, M.6
Cossart, P.7
Wolfrum, U.8
Petit, C.9
-
43
-
-
0029794058
-
Human Usher IB/mouse shaker-1; the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells
-
El-Amraoui, A., Sahly, I., Picaud, S., Sahel, J., Abitbol, M. and Petit, C. (1996) Human Usher IB/mouse shaker-1; the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells. Hum. Mol. Genet., 5, 1171-1178.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1171-1178
-
-
El-Amraoui, A.1
Sahly, I.2
Picaud, S.3
Sahel, J.4
Abitbol, M.5
Petit, C.6
-
44
-
-
0030801999
-
Expression of myosin VIIA during mouse embryogenesis
-
Sahly, I., El-Amraoui, A., Abitbol, M., Petit, C. and Dufier, J.-L. (1997) Expression of myosin VIIA during mouse embryogenesis. Anat. Embryol., 196, 159-170.
-
(1997)
Anat. Embryol.
, vol.196
, pp. 159-170
-
-
Sahly, I.1
El-Amraoui, A.2
Abitbol, M.3
Petit, C.4
Dufier, J.-L.5
|