Cohen-Salmon M - Search Results

1

Dynamic local mRNA localization and translation occurs during the postnatal molecular maturation of perivascular astrocytic processes.

Avila-Gutierrez K, Slaoui L, Alvear-Perez R, Kozlowski E, Oudart M, Augustin E, Claveau C, Mailly P, Monnet H, Mignon V, Saubaméa B, Boulay AC, Cohen-Salmon M. Avila-Gutierrez K, et al. Among authors: cohen salmon m. Glia. 2024 Apr;72(4):777-793. doi: 10.1002/glia.24503. Epub 2024 Jan 8. Glia. 2024. PMID: 38189217

2

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.

3

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

4

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.

5

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.

6

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

7

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.

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

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

10

Deletion of astroglial connexins weakens the blood-brain barrier.

Ezan P, André P, Cisternino S, Saubaméa B, Boulay AC, Doutremer S, Thomas MA, Quenech'du N, Giaume C, Cohen-Salmon M. Ezan P, et al. J Cereb Blood Flow Metab. 2012 Aug;32(8):1457-67. doi: 10.1038/jcbfm.2012.45. Epub 2012 Apr 4. J Cereb Blood Flow Metab. 2012. PMID: 22472609 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

66 results

Search Page

Filters