Sahly I - Search Results

1

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: sahly i. 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.

2

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: sahly i. Hum Mol Genet. 1996 Aug;5(8):1171-8. doi: 10.1093/hmg/5.8.1171. Hum Mol Genet. 1996. PMID: 8842737

3

Expression of myosin VIIA during mouse embryogenesis.

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

4

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: sahly i. 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.

5

The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route.

Papal S, Cortese M, Legendre K, Sorusch N, Dragavon J, Sahly I, Shorte S, Wolfrum U, Petit C, El-Amraoui A. Papal S, et al. Among authors: sahly i. Hum Mol Genet. 2013 Sep 15;22(18):3773-88. doi: 10.1093/hmg/ddt228. Epub 2013 May 23. Hum Mol Genet. 2013. PMID: 23704327

6

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.

Sahly I, Dufour E, Schietroma C, Michel V, Bahloul A, Perfettini I, Pepermans E, Estivalet A, Carette D, Aghaie A, Ebermann I, Lelli A, Iribarne M, Hardelin JP, Weil D, Sahel JA, El-Amraoui A, Petit C. Sahly I, et al. J Cell Biol. 2012 Oct 15;199(2):381-99. doi: 10.1083/jcb.201202012. Epub 2012 Oct 8. J Cell Biol. 2012. PMID: 23045546 Free PMC article.

7

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family.

Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C, Weil D, Cruaud C, Sahly I, Leibovici M, Bitner-Glindzicz M, Francis M, Lacombe D, Vigneron J, Charachon R, Boven K, Bedbeder P, Van Regemorter N, Weissenbach J, Petit C. Abdelhak S, et al. Among authors: sahly i. Nat Genet. 1997 Feb;15(2):157-64. doi: 10.1038/ng0297-157. Nat Genet. 1997. PMID: 9020840

8

SOX22 is a new member of the SOX gene family, mainly expressed in human nervous tissue.

Jay P, Sahly I, Gozé C, Taviaux S, Poulat F, Couly G, Abitbol M, Berta P. Jay P, et al. Among authors: sahly i. Hum Mol Genet. 1997 Jul;6(7):1069-77. doi: 10.1093/hmg/6.7.1069. Hum Mol Genet. 1997. PMID: 9215677

9

The zebrafish eya1 gene and its expression pattern during embryogenesis.

Sahly I, Andermann P, Petit C. Sahly I, et al. Dev Genes Evol. 1999 Jul;209(7):399-410. doi: 10.1007/s004270050270. Dev Genes Evol. 1999. PMID: 10370123

10

Prominent neuronal-specific tub gene expression in cellular targets of tubby mice mutation.

Sahly I, Gogat K, Kobetz A, Marchant D, Menasche M, Castel M, Revah F, Dufier J, Guerre-Millo M, Abitbol MM. Sahly I, et al. Hum Mol Genet. 1998 Sep;7(9):1437-47. doi: 10.1093/hmg/7.9.1437. Hum Mol Genet. 1998. PMID: 9700199

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