Resultados de búsqueda - Isabelle Aknin
- Mostrando 1 - 8 Resultados de 8
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Human and mouse ZFY genes produce a conserved testis-specific transcript encoding a zinc finger protein with a short acidic domain and modified transactivation potential por Fanny Decarpentrie, Nadège Vernet, Shantha K. Mahadevaiah, Guy Longepied, Eric Streichemberger, Isabelle Aknin‐Seifer, Obah A. Ojarikre, Paul S. Burgoyne, Catherine Metzler-Guillemain, Michael Mitchell
Publicado 2012Artigo -
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Lack of Association between Genetic Polymorphisms in Enzymes Associated with Folate Metabolism and Unexplained Reduced Sperm Counts por Célia Ravel, Sandra Chantot‐Bastaraud, Clémentine Chalmey, Luis B. Barreiro, Isabelle Aknin‐Seifer, Jérôme Pfeffer, Isabelle Berthaut, E. Emmanuelle Mathieu, Jacqueline Mandelbaum, Jean‐Pierre Siffroi, Ken McElreavey, Anu Bashamboo
Publicado 2009Artigo -
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Blue Light Exposure: Ocular Hazards and Prevention—A Narrative Review por Audrey Cougnard‐Grégoire, Bénédicte M. J. Merle, Tariq Aslam, Johanna M. Seddon, Isabelle Aknin, Caroline C. W. Klaver, Gerhard Garhöfer, Alfredo García‐Layana, Angelo Maria Minnella, Rufino Silva, Cécile Delcourt
Publicado 2023Revisão -
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Sedentary behavior, physical inactivity and body composition in relation to idiopathic infertility among men and women por Aude-Marie Foucaut, Céline Faure, Chantal Julia, Sébastien Czernichow, Rachel Lévy, Charlotte Dupont, Isabelle Aknin, Isabelle Cédrin‐Durnerin, Steven Cens, Pascale Chavatte‐Palmer, Serge Herçberg, Khaled Pocate, Nathalie Sermondade, Claude Uthurriague, Jean‐Philippe Wolf, Alifert Collaborative Group
Publicado 2019Artigo -
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A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family por Özlem Okutman, Jean Muller, Valerie Skory, Jean Marie Garnier, Angéline Gaucherot, Yoni Baert, Valérie Lamour, Münevver Serdarogullari, Meral Gültomruk, Albrecht Röpke, Sabine Kliesch, V. Granados Herbepin, Isabelle Aknin, Moncef Benkhalifa, Marius Teletin, Emre Bakırcıoğlu, Ellen Goossens, Nicolas Charlet‐Berguerand, Mustafa Bahçeci, Frank Tüttelmann, Stéphane Viville
Publicado 2017Artigo -
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Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background por Csilla Krausz, Claudia Giachini, Yali Xue, Moira K. O’Bryan, Jörg Gromoll, Ewa Rajpert‐De Meyts, Rafael Oliva, Isabelle Aknin‐Seifer, E. Erdei, Niels Jørgensen, Manuela Simoni, J. L. Ballescà, Roei Levy, Giancarlo Balercia, Paola Piomboni, Eberhard Nieschlag, Gianni Forti, Robert I. McLachlan, Chris Tyler‐Smith
Publicado 2008Artigo -
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<scp>SPINK</scp>2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes por Zine‐Eddine Kherraf, Marie Christou‐Kent, Thomas Karaouzène, Amir Amiri‐Yekta, Guillaume Martinez, Alexandra Vargas, Emeline Lambert, Christelle Borel, Béatrice Dorphin, Isabelle Aknin‐Seifer, Michael Mitchell, Catherine Metzler‐Guillemain, Jessica Escoffier, Serge Nef, Mariane Grepillat, Nicolas Thierry‐Mieg, Véronique Satre, M. Bailly, Florence Boitrelle, Karin Pernet‐Gallay, Sylviane Hennebicq, Julien Fauré, Serge P. Bottari, Charles Coutton, Pierre F. Ray, Christophe Arnoult
Publicado 2017Artigo
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