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I Sahly

Showing results (1-10 of 13) with videos related to

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Development Genes and Evolution|June 17, 1999
The zebrafish eya1 gene and its expression pattern during embryogenesisI Sahly, P Andermann, C Petit
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 16, 1998
Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndromeV Kalatzis, I Sahly, A El-Amraoui, et al.
Visual Neuroscience|July 1, 1994
Accumulation of calcium in degenerating photoreceptors of several Drosophila mutantsI Sahly, W H Schröder, K Zierold, et al.
Journal of Neuroscience Methods|June 20, 2003
Effective expression of the green fluorescent fusion proteins in cultured Aplysia neuronsI Sahly, H Erez, A Khoutorsky, et al.
Anatomy and Embryology|August 1, 1997
Expression of myosin VIIA during mouse embryogenesisI Sahly, A El-Amraoui, M Abitbol, et al.
Human Molecular Genetics|August 1, 1996
Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cellsA el-Amraoui, I Sahly, S Picaud, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Phorbol ester induces photoreceptor-specific degeneration in a Drosophila mutantB Minke, C T Rubinstein, I Sahly, et al.
Human Molecular Genetics|July 1, 1997
SOX22 is a new member of the SOX gene family, mainly expressed in human nervous tissueP Jay, I Sahly, C Gozé, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Calcium channel blockers inhibit retinal degeneration in the retinal-degeneration-B mutant of DrosophilaI Sahly, S Bar Nachum, E Suss-Toby, et al.
Human Mutation|March 1, 2000
Identification of novel PAX6 mutations in two families with bilateral aniridia. Mutations in brief no. 167. OnlineM Neuner-Jehle, F Munier, A Kobetz, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Development Genes and Evolution|June 17, 1999
The zebrafish eya1 gene and its expression pattern during embryogenesisI Sahly, P Andermann, C Petit
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 16, 1998
Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndromeV Kalatzis, I Sahly, A El-Amraoui, et al.
Visual Neuroscience|July 1, 1994
Accumulation of calcium in degenerating photoreceptors of several Drosophila mutantsI Sahly, W H Schröder, K Zierold, et al.
Journal of Neuroscience Methods|June 20, 2003
Effective expression of the green fluorescent fusion proteins in cultured Aplysia neuronsI Sahly, H Erez, A Khoutorsky, et al.
Anatomy and Embryology|August 1, 1997
Expression of myosin VIIA during mouse embryogenesisI Sahly, A El-Amraoui, M Abitbol, et al.
Human Molecular Genetics|August 1, 1996
Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cellsA el-Amraoui, I Sahly, S Picaud, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Phorbol ester induces photoreceptor-specific degeneration in a Drosophila mutantB Minke, C T Rubinstein, I Sahly, et al.
Human Molecular Genetics|July 1, 1997
SOX22 is a new member of the SOX gene family, mainly expressed in human nervous tissueP Jay, I Sahly, C Gozé, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Calcium channel blockers inhibit retinal degeneration in the retinal-degeneration-B mutant of DrosophilaI Sahly, S Bar Nachum, E Suss-Toby, et al.
Human Mutation|March 1, 2000
Identification of novel PAX6 mutations in two families with bilateral aniridia. Mutations in brief no. 167. OnlineM Neuner-Jehle, F Munier, A Kobetz, et al.
Pageof 2