Cohen-Salmon M - Search Results

1

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. 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.

2

Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.

El-Amraoui A, Cohen-Salmon M, Petit C, Simmler MC. El-Amraoui A, et al. Hear Res. 2001 Aug;158(1-2):151-9. doi: 10.1016/s0378-5955(01)00312-4. Hear Res. 2001. PMID: 11506947

3

Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear.

Cohen-Salmon M, Maxeiner S, Krüger O, Theis M, Willecke K, Petit C. Cohen-Salmon M, et al. Cell Tissue Res. 2004 Apr;316(1):15-22. doi: 10.1007/s00441-004-0861-2. Epub 2004 Feb 20. Cell Tissue Res. 2004. PMID: 14986102

4

Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis.

Cohen-Salmon M, Regnault B, Cayet N, Caille D, Demuth K, Hardelin JP, Janel N, Meda P, Petit C. Cohen-Salmon M, et al. Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6229-34. doi: 10.1073/pnas.0605108104. Epub 2007 Mar 30. Proc Natl Acad Sci U S A. 2007. PMID: 17400755 Free PMC article.

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. Nat Genet. 1999 Apr;21(4):363-9. doi: 10.1038/7693. Nat Genet. 1999. PMID: 10192385

6

Mapping of the otogelin gene (OTGN) to mouse chromosome 7 and human chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18.

Cohen-Salmon M, Mattei MG, Petit C. Cohen-Salmon M, et al. Mamm Genome. 1999 May;10(5):520-2. doi: 10.1007/s003359901033. Mamm Genome. 1999. PMID: 10337628 No abstract available.

7

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. Nat Genet. 2000 Feb;24(2):139-43. doi: 10.1038/72793. Nat Genet. 2000. PMID: 10655058

8

Fdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchyme.

Cohen-Salmon M, Frenz D, Liu W, Verpy E, Voegeling S, Petit C. Cohen-Salmon M, et al. J Biol Chem. 2000 Dec 22;275(51):40036-41. doi: 10.1074/jbc.M002876200. J Biol Chem. 2000. PMID: 10998416 Free article.

9

Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death.

Cohen-Salmon M, Ott T, Michel V, Hardelin JP, Perfettini I, Eybalin M, Wu T, Marcus DC, Wangemann P, Willecke K, Petit C. Cohen-Salmon M, et al. Curr Biol. 2002 Jul 9;12(13):1106-11. doi: 10.1016/s0960-9822(02)00904-1. Curr Biol. 2002. PMID: 12121617 Free PMC article.

10

Cloning and characterization of the mouse collapsin response mediator protein-1, Crmp1.

Cohen-Salmon M, Crozet F, Rebillard G, Petit C. Cohen-Salmon M, et al. Mamm Genome. 1997 May;8(5):349-51. doi: 10.1007/s003359900438. Mamm Genome. 1997. PMID: 9107681 No abstract available.

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