CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival-Reference-Cited by-同舟云学术

CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival

Published:2017-12 Issue:12 Volume:9 Page:1711-1731
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Michel Vincent¹²³,Booth Kevin T⁴⁵,Patni Pranav¹²³,Cortese Matteo¹²³,Azaiez Hela⁴,Bahloul Amel¹²³,Kahrizi Kimia⁶,Labbé Ménélik¹²³,Emptoz Alice¹²³,Lelli Andrea¹²³,Dégardin Julie³⁷,Dupont Typhaine¹²³,Aghaie Asadollah¹²³⁸,Oficjalska‐Pham Danuta¹²³,Picaud Serge³⁷,Najmabadi Hossein⁶,Smith Richard J⁴,Bowl Michael R⁹,Brown Steven DM⁹,Avan Paul¹⁰,Petit Christine¹²³¹¹,El‐Amraoui Aziz¹²³^ORCID

Affiliation:

1. Génétique et Physiologie de l'Audition Institut Pasteur Paris France

2. Unité Mixte de Recherche‐ UMRS 1120 Institut National de la Santé et de la Recherche Médicale Paris France

3. Sorbonne Universités UPMC Univ Paris06 Paris France

4. Molecular Otolaryngology and Renal Research Laboratories Department of Otolaryngology‐ Head and Neck Surgery University of Iowa Iowa City Iowa

5. Department of Molecular Medicine Carver College of Medicine University of Iowa Iowa City Iowa

6. Genetics Research Center University of Social Welfare and Rehabilitation Sciences Tehran Iran

7. Retinal information processing – Pharmacology and Pathology Institut de la Vision Paris France

8. Syndrome de Usher et Autres Atteintes Rétino‐Cochléaires Institut de la Vision Paris France

9. Mammalian Genetics Unit MRC Harwell Institute Oxford UK

10. Laboratoire de Biophysique Sensorielle Faculté de Médecine Biophysique Médicale, Centre Jean Perrin Université d'Auvergne Clermont‐Ferrand France

11. Collège de France Paris France

Funder

European Commission

Seventh Framework Programme

Horizon 2020 Framework Programme

Agence Nationale de la Recherche

Fondation BNP Paribas

Medical Research Council

Iran National Science Foundation

National Institute on Deafness and Other Communication Disorders

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201708087

Reference94 articles.

1. USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses

2. Interactions in the network of Usher syndrome type 1 proteins

3. Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

4. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

5. TBC1D24Mutation Causes Autosomal-Dominant Nonsyndromic Hearing Loss

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2. CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase pattern;2024-07-31

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