Cohen-Salmon M - Search Results

1

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

2

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome.

del Castillo I, Cohen-Salmon M, Blanchard S, Lutfalla G, Petit C. del Castillo I, et al. Nat Genet. 1992 Dec;2(4):305-10. doi: 10.1038/ng1292-305. Nat Genet. 1992. PMID: 1303284

3

Characterization of the promoter of the human KAL gene, responsible for the X-chromosome-linked Kallmann syndrome.

Cohen-Salmon M, Tronche F, del Castillo I, Petit C. Cohen-Salmon M, et al. Gene. 1995 Oct 27;164(2):235-42. doi: 10.1016/0378-1119(95)00481-k. Gene. 1995. PMID: 7590336

4

Isolation and characterization of the gene responsible for the X chromosome-linked Kallmann syndrome.

Legouis R, Cohen-Salmon M, Del Castillo I, Petit C. Legouis R, et al. Biomed Pharmacother. 1994;48(5-6):241-6. doi: 10.1016/0753-3322(94)90139-2. Biomed Pharmacother. 1994. PMID: 7999985 Review.

5

Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndrome.

Legouis R, Cohen-Salmon M, del Castillo I, Levilliers J, Capy L, Mornow JP, Petit C. Legouis R, et al. Genomics. 1993 Aug;17(2):516-8. doi: 10.1006/geno.1993.1360. Genomics. 1993. PMID: 8406507

6

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.

7

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.

8

Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndrome.

Hardelin JP, Soussi-Yanicostas N, Levilliers J, Kalatzis V, Abdelhak S, Cohen-Salmon M, Petit C. Hardelin JP, et al. Adv Nephrol Necker Hosp. 1998;28:419-28. Adv Nephrol Necker Hosp. 1998. PMID: 9890002 Review. No abstract available.

9

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.

10

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

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