Abitbol M - 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: abitbol m. 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: abitbol m. 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. Among authors: abitbol m. Anat Embryol (Berl). 1997 Aug;196(2):159-70. doi: 10.1007/s004290050088. Anat Embryol (Berl). 1997. PMID: 9278160

4

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: abitbol m. Hum Mol Genet. 1997 Jul;6(7):1069-77. doi: 10.1093/hmg/6.7.1069. Hum Mol Genet. 1997. PMID: 9215677

5

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. Among authors: abitbol mm. Hum Mol Genet. 1998 Sep;7(9):1437-47. doi: 10.1093/hmg/7.9.1437. Hum Mol Genet. 1998. PMID: 9700199

6

Identification of novel PAX6 mutations in two families with bilateral aniridia. Mutations in brief no. 167. Online.

Neuner-Jehle M, Munier F, Kobetz A, Sahly I, Uteza Y, Mermoud A, Schorderet DF, Dufier JL, Abitbol M. Neuner-Jehle M, et al. Among authors: abitbol m. Hum Mutat. 1998;12(2):138. doi: 10.1002/(SICI)1098-1004(1998)12:2<138::AID-HUMU17>3.0.CO;2-D. Hum Mutat. 1998. PMID: 10694925

7

Identification of a novel PAX6 gene mutation in an aniridia patient.

Sahly I, Abitbol M, Laurent C, Ghazi I, Ribeaudeau F, Vekemans M, Dufier JL. Sahly I, et al. Among authors: abitbol m. Hum Mutat. 1996;7(4):377. doi: 10.1002/humu.1380070403. Hum Mutat. 1996. PMID: 8723696 No abstract available.

8

Intravitreous transplantation of encapsulated fibroblasts secreting the human fibroblast growth factor 2 delays photoreceptor cell degeneration in Royal College of Surgeons rats.

Uteza Y, Rouillot JS, Kobetz A, Marchant D, Pecqueur S, Arnaud E, Prats H, Honiger J, Dufier JL, Abitbol M, Neuner-Jehle M. Uteza Y, et al. Among authors: abitbol m. Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):3126-31. doi: 10.1073/pnas.96.6.3126. Proc Natl Acad Sci U S A. 1999. PMID: 10077648 Free PMC article.

9

Expression of the SOX10 gene during human development.

Bondurand N, Kobetz A, Pingault V, Lemort N, Encha-Razavi F, Couly G, Goerich DE, Wegner M, Abitbol M, Goossens M. Bondurand N, et al. Among authors: abitbol m. FEBS Lett. 1998 Aug 7;432(3):168-72. doi: 10.1016/s0014-5793(98)00843-6. FEBS Lett. 1998. PMID: 9720918 Free article.

10

Prosaposin gene expression in normal and dystrophic RCS rat retina.

Van Den Berghe L, Sainton K, Gogat K, Marchant D, Dufour E, Bonnel S, Gadin S, Menasche M, Abitbol M. Van Den Berghe L, et al. Among authors: abitbol m. Invest Ophthalmol Vis Sci. 2004 May;45(5):1297-305. doi: 10.1167/iovs.03-1048. Invest Ophthalmol Vis Sci. 2004. PMID: 15111580

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