Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain

Protocadherin 15 (PCDH15) is expressed in hair cells of the inner ear and in photoreceptors of the retina. Mutations in PCDH15 cause Usher Syndrome (deaf-blindness) and recessive deafness. In developing hair cells, PCDH15 localizes to extracellular linkages that connect the stereocilia and kinociliu...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Webb, Stuart W., Grillet, Nicolas, Andrade, Leonardo R., Xiong, Wei, Swarthout, Lani, Della Santina, Charley C., Kachar, Bechara, Müller, Ulrich
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Company of Biologists 2011
Θέματα:
Research Articles
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3062428/
https://ncbi.nlm.nih.gov/pubmed/21427143
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.060061
Ετικέτες: Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!

Παρόμοια τεκμήρια