Literature DB >> 28739901

Profile of Christine Petit.

Tinsley H Davis.   

Abstract

Year:  2017        PMID： 28739901      PMCID： PMC5547658          DOI： 10.1073/pnas.1711360114

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  18 in total

1.  Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

Authors:  F Denoyelle; S Marlin; D Weil; L Moatti; P Chauvin; E N Garabédian; C Petit
Journal:  Lancet       Date:  1999-04-17       Impact factor: 79.321

2.  Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons.

Authors:  Nadia Soussi-Yanicostas; Fernando de Castro; A Karyn Julliard; Isabelle Perfettini; Alain Chédotal; Christine Petit
Journal:  Cell       Date:  2002-04-19       Impact factor: 41.582

3.  Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane.

Authors:  Elisabeth Verpy; Michel Leibovici; Nicolas Michalski; Richard J Goodyear; Carine Houdon; Dominique Weil; Guy P Richardson; Christine Petit
Journal:  J Comp Neurol       Date:  2011-02-01       Impact factor: 3.215

4.  A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family.

Authors:  S Abdelhak; V Kalatzis; R Heilig; S Compain; D Samson; C Vincent; D Weil; C Cruaud; I Sahly; M Leibovici; M Bitner-Glindzicz; M Francis; D Lacombe; J Vigneron; R Charachon; K Boven; P Bedbeder; N Van Regemorter; J Weissenbach; C Petit
Journal:  Nat Genet       Date:  1997-02       Impact factor: 38.330

5.  Defective myosin VIIA gene responsible for Usher syndrome type 1B.

Authors:  D Weil; S Blanchard; J Kaplan; P Guilford; F Gibson; J Walsh; P Mburu; A Varela; J Levilliers; M D Weston
Journal:  Nature       Date:  1995-03-02       Impact factor: 49.962

6.  An abnormal terminal X-Y interchange accounts for most but not all cases of human XX maleness.

Authors:  C Petit; A de la Chapelle; J Levilliers; S Castillo; B Noël; J Weissenbach
Journal:  Cell       Date:  1987-06-05       Impact factor: 41.582

7.  The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.

Authors:  R Legouis; J P Hardelin; J Levilliers; J M Claverie; S Compain; V Wunderle; P Millasseau; D Le Paslier; D Cohen; D Caterina
Journal:  Cell       Date:  1991-10-18       Impact factor: 41.582

8.  Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes.

Authors:  Sedigheh Delmaghani; Jean Defourny; Asadollah Aghaie; Maryline Beurg; Didier Dulon; Nicolas Thelen; Isabelle Perfettini; Tibor Zelles; Mate Aller; Anaïs Meyer; Alice Emptoz; Fabrice Giraudet; Michel Leibovici; Sylvie Dartevelle; Guillaume Soubigou; Marc Thiry; E Sylvester Vizi; Saaid Safieddine; Jean-Pierre Hardelin; Paul Avan; Christine Petit
Journal:  Cell       Date:  2015-11-05       Impact factor: 41.582

9.  A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

Authors:  P Guilford; S Ben Arab; S Blanchard; J Levilliers; J Weissenbach; A Belkahia; C Petit
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330

10.  Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system.

Authors:  N Soussi-Yanicostas; J P Hardelin; M M Arroyo-Jimenez; O Ardouin; R Legouis; J Levilliers; F Traincard; J M Betton; L Cabanié; C Petit
Journal:  J Cell Sci       Date:  1996-07       Impact factor: 5.285
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