Showing results (11-20 of 19) with videos related to
Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
The Journal of Biological Chemistry|July 13, 2000
Unconventional myosin VIIA is a novel A-kinase-anchoring proteinP Küssel-Andermann, A El-Amraoui, S Safieddine, et al.Proceedings of the National Academy of Sciences of the United States of America|April 13, 2000
KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathwayT Kharkovets, J P Hardelin, S Safieddine, et al.Nature Genetics|February 2, 2000
Targeted disruption of otog results in deafness and severe imbalanceM C Simmler, M Cohen-Salmon, A El-Amraoui, et al.Cell|February 20, 1999
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafnessC Kubisch, B C Schroeder, T Friedrich, et al.The EMBO Journal|November 18, 2000
Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complexP Küssel-Andermann, A El-Amraoui, S Safieddine, et al.Nature Genetics|April 7, 1999
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafnessS Yasunaga, M Grati, M Cohen-Salmon, et al.Proceedings of the National Academy of Sciences of the United States of America|April 16, 1996
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epitheliaD Weil, G Levy, I Sahly, et al.Clinical Genetics|November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1JK T Booth, K Kahrizi, M Babanejad, et al.Genomics|March 1, 1997
Cloning of the genes encoding two murine and human cochlear unconventional type I myosinsF Crozet, A el Amraoui, S Blanchard, et al.Pageof 2