Petit C - Search Results

1

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

Michel V, Booth KT, Patni P, Cortese M, Azaiez H, Bahloul A, Kahrizi K, Labbé M, Emptoz A, Lelli A, Dégardin J, Dupont T, Aghaie A, Oficjalska-Pham D, Picaud S, Najmabadi H, Smith RJ, Bowl MR, Brown SD, Avan P, Petit C, El-Amraoui A. Michel V, et al. Among authors: petit c. EMBO Mol Med. 2017 Dec;9(12):1711-1731. doi: 10.15252/emmm.201708087. EMBO Mol Med. 2017. PMID: 29084757 Free PMC article.

2

Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.

Weil D, Levy G, Sahly I, Levi-Acobas F, Blanchard S, El-Amraoui A, Crozet F, Philippe H, Abitbol M, Petit C. Weil D, et al. Among authors: petit c. Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3232-7. doi: 10.1073/pnas.93.8.3232. Proc Natl Acad Sci U S A. 1996. PMID: 8622919 Free PMC article.

3

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells.

el-Amraoui A, Sahly I, Picaud S, Sahel J, Abitbol M, Petit C. el-Amraoui A, et al. Among authors: petit c. Hum Mol Genet. 1996 Aug;5(8):1171-8. doi: 10.1093/hmg/5.8.1171. Hum Mol Genet. 1996. PMID: 8842737

4

Expression of myosin VIIA during mouse embryogenesis.

Sahly I, El-Amraoui A, Abitbol M, Petit C, Dufier JL. Sahly I, et al. Among authors: petit c. Anat Embryol (Berl). 1997 Aug;196(2):159-70. doi: 10.1007/s004290050088. Anat Embryol (Berl). 1997. PMID: 9278160

5

Otogelin: a glycoprotein specific to the acellular membranes of the inner ear.

Cohen-Salmon M, El-Amraoui A, Leibovici M, Petit C. Cohen-Salmon M, et al. Among authors: petit c. Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14450-5. doi: 10.1073/pnas.94.26.14450. Proc Natl Acad Sci U S A. 1997. PMID: 9405633 Free PMC article.

6

Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome.

Kalatzis V, Sahly I, El-Amraoui A, Petit C. Kalatzis V, et al. Among authors: petit c. Dev Dyn. 1998 Dec;213(4):486-99. doi: 10.1002/(SICI)1097-0177(199812)213:4<486::AID-AJA13>3.0.CO;2-L. Dev Dyn. 1998. PMID: 9853969 Free article.

7

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness.

Kubisch C, Schroeder BC, Friedrich T, Lütjohann B, El-Amraoui A, Marlin S, Petit C, Jentsch TJ. Kubisch C, et al. Among authors: petit c. Cell. 1999 Feb 5;96(3):437-46. doi: 10.1016/s0092-8674(00)80556-5. Cell. 1999. PMID: 10025409 Free article.

8

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

9

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

10

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.

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