Chardenoux S - Search Results

1

A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23.

Chaïb H, Place C, Salem N, Chardenoux S, Vincent C, Weissenbach J, El-Zir E, Loiselet J, Petit C. Chaïb H, et al. Among authors: chardenoux s. Hum Mol Genet. 1996 Jan;5(1):155-8. doi: 10.1093/hmg/5.1.155. Hum Mol Genet. 1996. PMID: 8789454

2

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

Chaib H, Place C, Salem N, Dodé C, Chardenoux S, Weissenbach J, el Zir E, Loiselet J, Petit C. Chaib H, et al. Among authors: chardenoux s. Hum Mol Genet. 1996 Jul;5(7):1061-4. doi: 10.1093/hmg/5.7.1061. Hum Mol Genet. 1996. PMID: 8817348

3

A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.

Mustapha M, Chardenoux S, Nieder A, Salem N, Weissenbach J, el-Zir E, Loiselet J, Petit C. Mustapha M, et al. Among authors: chardenoux s. Eur J Hum Genet. 1998 May-Jun;6(3):245-50. doi: 10.1038/sj.ejhg.5200177. Eur J Hum Genet. 1998. PMID: 9781028

4

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

Mustapha M, Weil D, Chardenoux S, Elias S, El-Zir E, Beckmann JS, Loiselet J, Petit C. Mustapha M, et al. Among authors: chardenoux s. Hum Mol Genet. 1999 Mar;8(3):409-12. doi: 10.1093/hmg/8.3.409. Hum Mol Genet. 1999. PMID: 9949200

5

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: chardenoux s. 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.

6

A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.

Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Armenta D, Lathrop M, Petit C, Moreno F. Modamio-Høybjør S, et al. Among authors: chardenoux s. Hum Genet. 2003 Jan;112(1):24-8. doi: 10.1007/s00439-002-0836-x. Epub 2002 Oct 16. Hum Genet. 2003. PMID: 12483295

7

Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates.

Ben Arab S, Hmani M, Denoyelle F, Boulila-Elgaied A, Chardenoux S, Hachicha S, Petit C, Ayadi H. Ben Arab S, et al. Among authors: chardenoux s. Clin Genet. 2000 Jun;57(6):439-43. doi: 10.1034/j.1399-0004.2000.570607.x. Clin Genet. 2000. PMID: 10905664

8

DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23.

Moreno-Pelayo MA, Modamio-Høybjør S, Mencía A, del Castillo I, Chardenoux S, Fernández-Burriel M, Lathrop M, Petit C, Moreno F. Moreno-Pelayo MA, et al. Among authors: chardenoux s. J Med Genet. 2003 Nov;40(11):832-6. doi: 10.1136/jmg.40.11.832. J Med Genet. 2003. PMID: 14627674 Free PMC article. No abstract available.

9

A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci.

Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Morais D, Lathrop M, Petit C, Moreno F. Modamio-Høybjør S, et al. Among authors: chardenoux s. J Med Genet. 2004 Feb;41(2):e14. doi: 10.1136/jmg.2003.012500. J Med Genet. 2004. PMID: 14757864 Free PMC article. No abstract available.

10

Mice humanized for MHC and hACE2 with high permissiveness to SARS-CoV-2 omicron replication.

Le Chevalier F, Authié P, Chardenoux S, Bourgine M, Vesin B, Cussigh D, Sassier Y, Fert I, Noirat A, Nemirov K, Anna F, Bérard M, Guinet F, Hardy D, Charneau P, Lemonnier F, Langa-Vives F, Majlessi L. Le Chevalier F, et al. Among authors: chardenoux s. Microbes Infect. 2023 Sep-Oct;25(7):105142. doi: 10.1016/j.micinf.2023.105142. Epub 2023 Apr 19. Microbes Infect. 2023. PMID: 37080384 Free PMC article.

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