A. Aghaie

发表

Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes

E. Vizi, P. Avan, C. Petit, 2015, Cell.

The Mitochondrial Protease AFG3L2 Is Essential for Axonal Development

J. Guénet, B. Taylor, G. Casari, 2008, The Journal of Neuroscience.

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

N. Ben-Tal, M. Lathrop, P. Avan, 2006, Nature Genetics.

Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.

C. Petit, S. Chardenoux, J. Hardelin, 2016, American journal of human genetics.

JCB_201612030 1..16

J. Sahel, S. Picaud, K. Parain, 2017 .

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

J. Sahel, C. Petit, D. Weil, 2012, The Journal of cell biology.

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

Steve D. M. Brown, P. Avan, S. Picaud, 2017, EMBO molecular medicine.

Usher syndrome type 1–associated cadherins shape the photoreceptor outer segment

J. Sahel, S. Picaud, K. Parain, 2017, The Journal of cell biology.

New Insights into the Alternative d-Glucarate Degradation Pathway*

Marcel Salanoubat, Gabor Gyapay, Delphine Muselet, 2008, Journal of Biological Chemistry.

crv 4 , a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 ( Grm 1 )

R. Ravazzolo, A. Fairén, M. Cilli, 2022 .

Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth

P. Avan, C. Petit, A. El-Amraoui, 2016, The Journal of cell biology.

Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.

C. Petit, D. Weil, N. Michalski, 2012, Human molecular genetics.

crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1).

Valerio Conti, Roberto Ravazzolo, Maura Castagna, 2006, International journal of molecular medicine.

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21–12.1

M. Lathrop, C. Petit, D. Weil, 2003, European Journal of Human Genetics.

The paralysé (par) mouse neurological mutation maps to a 9 Mbp (4 cM) interval of mouse chromosome 18

J. Guénet, A. Godard, A. Aghaie, 2005 .