Isabelle Perfettini

发表

Otoferlin, Defective in a Human Deafness Form, Is Essential for Exocytosis at the Auditory Ribbon Synapse

P. Avan, C. Petit, P. Rostaing, 2006, Cell.

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.

Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage

P. Avan, C. Petit, S. Delmaghani, 2019, Proceedings of the National Academy of Sciences.

Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death

K. Willecke, M. Cohen-Salmon, C. Petit, 2002, Current Biology.

Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes

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

Anosmin-1, Defective in the X-Linked Form of Kallmann Syndrome, Promotes Axonal Branch Formation from Olfactory Bulb Output Neurons

C. Petit, A. Chédotal, F. Castro, 2002, Cell.

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.

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

Pierre Legrain, Spencer Shorte, Jan Reiners, 2002, The EMBO journal.

PTEN inhibits AMPK to control collective migration

Flora Llense, K. Forsberg-Nilsson, E. Colucci-Guyon, 2021, Nature Communications.

An unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells

P. Avan, C. Petit, A. El-Amraoui, 2014, Proceedings of the National Academy of Sciences.

Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells.

Christine Petit, U. Wolfrum, C. Petit, 2005, Developmental biology.

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Steve D. M. Brown, A. Mallon, K. Steel, 2003, Nature Genetics.

Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells

P. Avan, C. Petit, D. Weil, 2009, EMBO molecular medicine.

Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin–catenins complex

U. Wolfrum, P. Cossart, C. Petit, 2000, The EMBO journal.

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.

Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly.

P. Legrain, C. Petit, A. El-Amraoui, 2005, Human molecular genetics.

Shroom2, a myosin-VIIa- and actin-binding protein, directly interacts with ZO-1 at tight junctions

P. Legrain, C. Petit, A. El-Amraoui, 2007, Journal of Cell Science.

Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells

C. Petit, Vincent Michel, J. Hardelin, 2020, Scientific Reports.

Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia

P. Avan, C. Petit, D. Weil, 2011, Proceedings of the National Academy of Sciences.