International audienceUsher syndrome type IIa (USH2A) combines moderate to severe congenital hearing impairment and retinitis pigmentosa. It is the most common genetic form of USH. USH2A encodes usherin, which was previously defined as a basement membrane protein. A much larger USH2A transcript predicted to encode a transmembrane (TM) isoform was recently reported. Here, we address the role of TM usherin in the inner ear. Analysis of the usherin alternative transcripts in the murine inner ear revealed the existence of several predicted TM usherin isoforms with modular ectodomains of different lengths. In addition, we identified in the usherin cytoplasmic region a predicted 24 amino acid peptide, derived from a newly defined exon that is pre...
scaffolding protein), underlie five forms of Usher syndrome type I (USH1). Mouse mutants for all the...
scaffolding protein), underlie five forms of Usher syndrome type I (USH1). Mouse mutants for all the...
International audienceSeveral lines of evidence indicate that very large G-protein-coupled receptor ...
International audienceDefects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 2...
The stereocilia bundle present at the apical surface of inner ear hair cells is the only device that...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
International audienceDefects in myosin VIIa, harmonin (a PDZ domain protein), cadherin 23, protocad...
Usher syndrome is the most common form of deaf-blindness. The syndrome is both clinically and geneti...
International audiencePurpose of review Usher syndrome (USH) is the most prevalent cause of heredita...
Usher syndrome is the most common form of deaf-blindness. The syndrome is both clinically and geneti...
AbstractUsher syndrome (USH), clinically and genetically heterogeneous, is the leading genetic cause...
scaffolding protein), underlie five forms of Usher syndrome type I (USH1). Mouse mutants for all the...
scaffolding protein), underlie five forms of Usher syndrome type I (USH1). Mouse mutants for all the...
International audienceSeveral lines of evidence indicate that very large G-protein-coupled receptor ...
International audienceDefects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 2...
The stereocilia bundle present at the apical surface of inner ear hair cells is the only device that...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
Defects in myosin VIIa, the PDZ-domain-containing protein harmonin, cadherin 23, protocadherin 15, a...
International audienceDefects in myosin VIIa, harmonin (a PDZ domain protein), cadherin 23, protocad...
Usher syndrome is the most common form of deaf-blindness. The syndrome is both clinically and geneti...
International audiencePurpose of review Usher syndrome (USH) is the most prevalent cause of heredita...
Usher syndrome is the most common form of deaf-blindness. The syndrome is both clinically and geneti...
AbstractUsher syndrome (USH), clinically and genetically heterogeneous, is the leading genetic cause...
scaffolding protein), underlie five forms of Usher syndrome type I (USH1). Mouse mutants for all the...
scaffolding protein), underlie five forms of Usher syndrome type I (USH1). Mouse mutants for all the...
International audienceSeveral lines of evidence indicate that very large G-protein-coupled receptor ...