S. Chardenoux

发表

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34

M. Lathrop, C. Petit, M. Mustapha, 2002, European Journal of Human Genetics.

A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36

Jean Weissenbach, Christine Petit, J. Weissenbach, 1998, European Journal of Human Genetics.

Brain cross‐protection against SARS‐CoV‐2 variants by a lentiviral vaccine in new transgenic mice

S. Chardenoux, K. Nemirov, P. Charneau, 2021, EMBO molecular medicine.

Full Brain and Lung Prophylaxis against SARS-CoV-2 by Intranasal Lentiviral Vaccination in a New hACE2 Transgenic Mouse Model or Golden Hamsters

S. Chardenoux, K. Nemirov, P. Charneau, 2021, bioRxiv.

Brain and Lung Cross-Protection against Ancestral or Emerging SARS-CoV-2 by Intranasal Lentiviral Vaccination in a New hACE2 Transgenic Murine Model

S. Chardenoux, K. Nemirov, P. Charneau, 2021 .

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.

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.

Aziz El-Amraoui, Christine Petit, C. Petit, 2005, Human molecular genetics.

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

J. Beckmann, C. Petit, M. Mustapha, 1999, Human molecular genetics.

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

J. Weissenbach, H. Chaib, C. Petit, 1996, Human molecular genetics.

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

C. Petit, S. Chardenoux, T. Friedman, 2000, American journal of human genetics.

A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23.

J. Weissenbach, C. Petit, S. Chardenoux, 1996, Human molecular genetics.

Mapping of DFNB 12 , a gene for a non-syndromal autosomal recessive deafness , to chromosome 10 q 21 – 22

J. Weissenbach, C. Petit, S. Chardenoux, 1996 .

Molecular Characterization of the Ankle-Link Complex in Cochlear Hair Cells and Its Role in the Hair Bundle Functioning

Makoto Sato, C. Petit, D. Weil, 2007, The Journal of Neuroscience.

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.

Mice Humanized for MHC and hACE2 with High Permissiveness to SARS-CoV-2 Omicron Replication

S. Chardenoux, F. Lemonnier, K. Nemirov, 2023, Microbes and Infection.

Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates

C. Petit, S. Chardenoux, F. Denoyelle, 2000, Clinical genetics.

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1

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

DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23

M. Lathrop, C. Petit, S. Chardenoux, 2003, Journal of medical genetics.