Petit C - Search Results

1

Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse.

Roux I, Safieddine S, Nouvian R, Grati M, Simmler MC, Bahloul A, Perfettini I, Le Gall M, Rostaing P, Hamard G, Triller A, Avan P, Moser T, Petit C. Roux I, et al. Among authors: petit c. Cell. 2006 Oct 20;127(2):277-89. doi: 10.1016/j.cell.2006.08.040. Cell. 2006. PMID: 17055430 Free article.

2

Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals.

Petit C, Levilliers J, Rouyer F, Simmler MC, Herouin E, Weissenbach J. Petit C, et al. Genomics. 1990 Apr;6(4):651-8. doi: 10.1016/0888-7543(90)90500-t. Genomics. 1990. PMID: 2341154

3

Normal and abnormal interchanges between the human X and Y chromosomes.

Weissenbach J, Levilliers J, Petit C, Rouyer F, Simmler MC. Weissenbach J, et al. Among authors: petit c. Development. 1987;101 Suppl:67-74. Development. 1987. PMID: 3503725

4

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.

Denoyelle F, Weil D, Maw MA, Wilcox SA, Lench NJ, Allen-Powell DR, Osborn AH, Dahl HH, Middleton A, Houseman MJ, Dodé C, Marlin S, Boulila-ElGaïed A, Grati M, Ayadi H, BenArab S, Bitoun P, Lina-Granade G, Godet J, Mustapha M, Loiselet J, El-Zir E, Aubois A, Joannard A, Levilliers J, Garabédian EN, Mueller RF, Gardner RJ, Petit C, et al. Denoyelle F, et al. Among authors: petit c. Hum Mol Genet. 1997 Nov;6(12):2173-7. doi: 10.1093/hmg/6.12.2173. Hum Mol Genet. 1997. PMID: 9336442

5

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.

Yasunaga S, Grati M, Cohen-Salmon M, El-Amraoui A, Mustapha M, Salem N, El-Zir E, Loiselet J, Petit C. Yasunaga S, et al. Among authors: petit c. Nat Genet. 1999 Apr;21(4):363-9. doi: 10.1038/7693. Nat Genet. 1999. PMID: 10192385

6

Targeted disruption of otog results in deafness and severe imbalance.

Simmler MC, Cohen-Salmon M, El-Amraoui A, Guillaud L, Benichou JC, Petit C, Panthier JJ. Simmler MC, et al. Among authors: petit c. Nat Genet. 2000 Feb;24(2):139-43. doi: 10.1038/72793. Nat Genet. 2000. PMID: 10655058

7

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

Kharkovets T, Hardelin JP, Safieddine S, Schweizer M, El-Amraoui A, Petit C, Jentsch TJ. Kharkovets T, et al. Among authors: petit c. Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4333-8. doi: 10.1073/pnas.97.8.4333. Proc Natl Acad Sci U S A. 2000. PMID: 10760300 Free PMC article.

8

DFNB9 and DFNB12.

Yasunaga S, Grati M, Petit C. Yasunaga S, et al. Among authors: petit c. Adv Otorhinolaryngol. 2000;56:164-7. doi: 10.1159/000059097. Adv Otorhinolaryngol. 2000. PMID: 10868229 Review. No abstract available.

9

Unconventional myosin VIIA is a novel A-kinase-anchoring protein.

Küssel-Andermann P, El-Amraoui A, Safieddine S, Hardelin JP, Nouaille S, Camonis J, Petit C. Küssel-Andermann P, et al. Among authors: petit c. J Biol Chem. 2000 Sep 22;275(38):29654-9. doi: 10.1074/jbc.M004393200. J Biol Chem. 2000. PMID: 10889203 Free article.

10

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

Yasunaga S, Grati M, Chardenoux S, Smith TN, Friedman TB, Lalwani AK, Wilcox ER, Petit C. Yasunaga S, et al. Among authors: petit c. Am J Hum Genet. 2000 Sep;67(3):591-600. doi: 10.1086/303049. Epub 2000 Jul 19. Am J Hum Genet. 2000. PMID: 10903124 Free PMC article.

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