Search Results - "Sahly, Iman"

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice by Sahly, Iman, Dufour, Eric, Schietroma, Cataldo, Michel, Vincent, Bahloul, Amel, Perfettini, Isabelle, Pepermans, Elise, Estivalet, Amrit, Carette, Diane, Aghaie, Asadollah, Ebermann, Inga, Lelli, Andrea, Iribarne, Maria, Hardelin, Jean-Pierre, Weil, Dominique, Sahel, José-Alain, El-Amraoui, Aziz, Petit, Christine

“…The mechanisms underlying retinal dystrophy in Usher syndrome type I (USH1) remain unknown because mutant mice lacking any of the USH1 proteins-myosin VIIa,…”
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Novel transgenic mice for inducible gene overexpression in pancreatic cells define glucocorticoid receptor-mediated regulations of beta cells by Blondeau, Bertrand, Sahly, Iman, Massouridès, Emmanuelle, Singh-Estivalet, Amrit, Valtat, Bérengère, Dorchene, Delphine, Jaisser, Frédéric, Bréant, Bernadette, Tronche, Francois

“…Conditional gene deletion in specific cell populations has helped the understanding of pancreas development. Using this approach, we have shown that deleting…”
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Combinatorial complexity of 5' alternative acetylcholinesterase transcripts and protein products by Meshorer, Eran, Toiber, Debra, Zurel, Dror, Sahly, Iman, Dori, Amir, Cagnano, Emanuela, Schreiber, Letizia, Grisaru, Dan, Tronche, François, Soreq, Hermona

“…To explore the scope and significance of alternate promoter usage and its putative inter-relationship to alternative splicing, we searched expression sequence…”
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A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family by Cruaud, Corinne, Leibovici, Michel, Compain, Sylvie, Lacombe, Didier, Bitner-Glindzicz, Maria, Vigneron, Jacqueline, Boven, Katia, Petit, Christine, Charachon, Robert, Francis, Mary, Weil, Dominique, Regemorter, Nicole Van, Samson, Delphine, Weissenbach, Jean, Bedbeder, Philippe, Heilig, Roland, Sahly, Iman, Abdelhak, Sonia, Kalatzis, Vasiliki, Vincent, Christophe

“…A candidate gene for Branchio-Oto-Renal (BOR) syndrome was identified at chromosome 8q13.3 by positional cloning and shown to underlie the disease. This gene…”
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Eya1 expression in the developing ear and kidney: Towards the understanding of the pathogenesis of branchio‐oto‐renal (BOR) syndrome by Kalatzis, Vasiliki, Sahly, Iman, El‐Amraoui, Aziz, Petit, Christine

“…Branchio‐Oto‐Renal (BOR) syndrome is an autosomal dominant, early developmental defect characterised by varying combinations of branchial (fistulas, sinuses,…”
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SOX22 is a New Member of the SOX Gene Family, Mainly Expressed in Human Nervous Tissue by Jay, Philippe, Sahly, Iman, Gozé, Catherine, Taviaux, Sylvie, Poulat, Francis, Couly, Gérard, Abitbol, Marc, Berta, Philippe

“…SOX (SRY box-containing) genes share a particular DNA-binding domain, called HMG, with the mammalian testis-determining gene SRY. Several SOX genes have…”
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Expression of myosin VIIA during mouse embryogenesis by Sahly, I, El-Amraoui, A, Abitbol, M, Petit, C, Dufier, J L

“…The gene encoding myosin VIIA is responsible for the mouse shaker-1 phenotype, which consists of deafness and balance deficiency related to cochlear and…”
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The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route by Papal, Samantha, Cortese, Matteo, Legendre, Kirian, Sorusch, Nasrin, Dragavon, Joseph, Sahly, Iman, Shorte, Spencer, Wolfrum, Uwe, Petit, Christine, El-Amraoui, Aziz

“…Mutations in the myosin VIIa gene cause Usher syndrome type IB (USH1B), characterized by deaf-blindness. A delay of opsin trafficking has been observed in the…”
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The giant spectrin [beta]V couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route by Papal, Samantha, Cortese, Matteo, Legendre, Kirian, Sorusch, Nasrin, Dragavon, Joseph, Sahly, Iman, Shorte, Spencer, Wolfrum, Uwe, Petit, Christine, El-Amraoui, Aziz

“…Mutations in the myosin VIIa gene cause Usher syndrome type IB (USH1B), characterized by deaf-blindness. A delay of opsin trafficking has been observed in the…”
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Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments by Trouillet, Alix, Dubus, Elisabeth, Dégardin, Julie, Estivalet, Amrit, Ivkovic, Ivana, Godefroy, David, García-Ayuso, Diego, Simonutti, Manuel, Sahly, Iman, Sahel, José A., El-Amraoui, Aziz, Petit, Christine, Picaud, Serge

“…Usher syndrome type 1 (USH1) is a major cause of inherited deafness and blindness in humans. The eye disorder is often referred to as retinitis pigmentosa,…”
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The GABAergic Gudden's dorsal tegmental nucleus: A new relay for serotonergic regulation of sleep-wake behavior in the mouse by Chazalon, Marine, Dumas, Sylvie, Bernard, Jean-François, Sahly, Iman, Tronche, François, de Kerchove d’Exaerde, Alban, Hamon, Michel, Adrien, Joëlle, Fabre, Véronique, Bonnavion, Patricia

“…Serotonin (5-HT) neurons are involved in wake promotion and exert a strong inhibitory influence on rapid eye movement (REM) sleep. Such effects have been…”
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A Subpopulation of Serotonergic Neurons That Do Not Express the 5‑HT1A Autoreceptor by Kiyasova, Vera, Bonnavion, Patricia, Scotto-Lomassese, Sophie, Fabre, Véronique, Sahly, Iman, Tronche, François, Deneris, Evan, Gaspar, Patricia, Fernandez, Sebastian P

“…5-HT neurons are topographically organized in the hindbrain, and have been implicated in the etiology and treatment of psychiatric diseases such as depression…”
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Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice: Usher 1 retinal pathogenesis by Sahly, Iman, Dufour, Eric, Schietroma, Cataldo, Michel, Vincent, Bahloul, Amel, Perfettini, Isabelle, Pepermans, Elise, Estivalet, Amrit, Carette, Diane, Aghaie, Asadollah, Ebermann, Inga, Lelli, Andrea, Iribarne, Maria, Hardelin, Jean-Pierre, Weil, Dominique, Sahel, José-Alain, El-Amraoui, Aziz, Petit, Christine

“…The mechanisms underlying retinal dystrophy in Usher syndrome type I (USH1) remain unknown because mutant mice lacking any of the USH1 proteins-myosin VIIa,…”
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On-line confocal imaging of the events leading to structural dedifferentiation of an axonal segment into a growth cone after axotomy by Sahly, Iman, Khoutorsky, Arkady, Erez, Hadas, Prager-Khoutorsky, Masha, Spira, Micha E.

“…The transformation of a transected axonal tip into a growth cone (GC) after axotomy is a critical step in the cascade of events leading to regeneration…”
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When reverse genetics meets physiology: the use of site-specific recombinases in mice by Tronche, François, Casanova, Emilio, Turiault, Marc, Sahly, Iman, Kellendonk, Christoph

“…The use of site-specific recombinases enables the precise introduction of defined genetic mutations into the mouse genome. In theory, any deletion, point…”
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The zebrafish eya1 gene and its expression pattern during embryogenesis by Sahly, I, Andermann, P, Petit, C

“…The eyes absent-like genes encode a group of putative transcriptional coactivators with a sole representative in Drosophila and several members in mammals…”
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Human Usher 1B/Mouse shaker-1: The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor Cells by El-Amraoui, Aziz, Sahly, Iman, Picaud, Serge, Sahel, José, Abitbol, Marc, Petit, Christine

“…Usher syndrome type I (USH1) associates severe congenital deafness, vestibular dysfunction and progressive retinitis pigmentosa leading to blindness. The gene…”
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Human Myosin VIIA Responsible for the Usher 1B Syndrome: A Predicted Membrane-Associated Motor Protein Expressed in Developing Sensory Epithelia by Weil, Dominique, Lévy, Gallia, Sahly, Iman, Lévi-Acobas, Fabienne, Blanchard, Stéphane, El-Amraoui, Aziz, Crozet, Fabien, Philippe, Hervé, Abitbol, Marc, Petit, Christine

“…The gene encoding human myosin VIIA is responsible for Usher syndrome type 1B (USH1B), a disease which associates profound congenital sensorineural deafness,…”
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5-HT1A-iCre, a new transgenic mouse line for genetic analyses of the serotonergic pathway by Sahly, Iman, Fabre, Véronique, Vyas, Sheela, Milet, Aude, Rouzeau, Jean-Denis, Hamon, Michel, Lazar, Monique, Tronche, François

“…The 5-HT1A receptor not only plays an important role in brain physiology but it may be also implicated in the etiology of behavioral disorders such as…”
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Combinatorial Complexity of 5′ Alternative Acetylcholinesterase Transcripts and Protein Products by Eran Meshorer, Debra Toiber, Dror Zurel, Iman Sahly, Amir Dori, Emanuela Cagnano, Letizia Schreiber, Dan Grisaru, François Tronche, Hermona Soreq

“…To explore the scope and significance of alternate promoter usage and its putative inter-relationship to alternative splicing, we searched expression sequence…”
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