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KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness
C Kubisch, BC Schroeder, T Friedrich, B Lütjohann, A El-Amraoui, ...
Cell 96 (3), 437-446, 1999
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness
S Yasunaga, M Grati, M Cohen-Salmon, A El-Amraoui, M Mustapha, ...
Nature genetics 21 (4), 363-369, 1999
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle
B Boëda, A El‐Amraoui, A Bahloul, R Goodyear, L Daviet, S Blanchard, ...
The EMBO journal 21 (24), 6689-6699, 2002
KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway
T Kharkovets, JP Hardelin, S Safieddine, M Schweizer, A El-Amraoui, ...
Proceedings of the National Academy of Sciences 97 (8), 4333-4338, 2000
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
P Mburu, M Mustapha, A Varela, D Weil, A El-Amraoui, RH Holme, ...
Nature genetics 34 (4), 421-428, 2003
Usher syndrome type IG (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin
D Weil, A El-Amraoui, S Masmoudi, M Mustapha, Y Kikkawa, S Lainé, ...
Human molecular genetics 12 (5), 463-471, 2003
Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin–catenins complex
P Küssel‐Andermann, A El‐Amraoui, S Safieddine, S Nouaille, I Perfettini, ...
The EMBO journal 19 (22), 6020-6029, 2000
Interactions in the network of Usher syndrome type 1 proteins
A Adato, V Michel, Y Kikkawa, J Reiners, KN Alagramam, D Weil, ...
Human molecular genetics 14 (3), 347-356, 2005
Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells
A El-Amraoui, C Petit
Journal of Cell Science 118 (20), 4593-4603, 2005
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia
D Weil, G Levy, I Sahly, F Levi-Acobas, S Blanchard, A El-Amraoui, ...
Proceedings of the National Academy of Sciences 93 (8), 3232-3237, 1996
MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes
A El‐Amraoui, JS Schonn, P Küssel‐Andermann, S Blanchard, C Desnos, ...
EMBO reports 3 (5), 463-470, 2002
Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells
A Adato, G Lefevre, B Delprat, V Michel, N Michalski, S Chardenoux, ...
Human molecular genetics 14 (24), 3921-3932, 2005
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly
B Delprat, V Michel, R Goodyear, Y Yamasaki, N Michalski, A El-Amraoui, ...
Human molecular genetics 14 (3), 401-410, 2005
Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites
C Desnos, JS Schonn, S Huet, VS Tran, A El-Amraoui, G Raposo, ...
The Journal of cell biology 163 (3), 559-570, 2003
Otogelin: a glycoprotein specific to the acellular membranes of the inner ear
M Cohen-Salmon, A El-Amraoui, M Leibovici, C Petit
Proceedings of the National Academy of Sciences 94 (26), 14450-14455, 1997
Human Usher 1B/Mouse shaker-1 : The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor …
A El-Amraoui, I Sahly, S Picaud, J Sahel, M Abitbol, C Petit
Human molecular genetics 5 (8), 1171-1178, 1996
The auditory hair cell ribbon synapse: from assembly to function
S Safieddine, A El-Amraoui, C Petit
Annual review of neuroscience 35, 509-528, 2012
Involvement of the Rab27 binding protein Slac2c/MyRIP in insulin exocytosis
L Waselle, T Coppola, M Fukuda, M Iezzi, A El-Amraoui, C Petit, ...
Molecular biology of the cell 14 (10), 4103-4113, 2003
Targeted disruption of otog results in deafness and severe imbalance
MC Simmler, M Cohen-Salmon, A El-Amraoui, L Guillaud, JC Benichou, ...
Nature genetics 24 (2), 139-143, 2000
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice
I Sahly, E Dufour, C Schietroma, V Michel, A Bahloul, I Perfettini, ...
Journal of Cell Biology 199 (2), 381-399, 2012
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