نتائج البحث - Moncef Benkhalifa
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- اذهب إلى الاصفحة التالية
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Zinc concentrations in serum and follicular fluid during ovarian stimulation and expression of Zn2+ transporters in human oocytes and cumulus cells حسب Y. Ménézo, Laurène Pluntz, J. Chouteau, Timur Gürgan, Aygül Demi̇rol, A. Dalleac, Moncef Benkhalifa
منشور في 2011Artigo -
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Methylation changes in mature sperm deoxyribonucleic acid from oligozoospermic men: assessment of genetic variants and assisted reproductive technology outcome حسب Debbie Montjean, Célia Ravel, Moncef Benkhalifa, P. Cohen-Bacrie, Isabelle Berthaut, Anu Bashamboo, Kenneth McElreavey
منشور في 2013Artigo -
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Impact of alcohol and cigarette smoking consumption in male fertility potential: Looks at lipid peroxidation, enzymatic antioxidant activities and sperm DNA damage حسب Smahane Aboulmaouahib, Aicha Madkour, Ismail Kaarouch, Omar Sefrioui, Brahim Saadani, Henri Copin, Moncef Benkhalifa, Noureddine Louanjli, Rachida Cadi
منشور في 2017Artigo -
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Follicular Fluid Growth Factors and Interleukin Profiling as Potential Predictors of IVF Outcomes حسب Molka, Bouricha, Gwladys, Bourdenet, Dorian, Bosquet, Lucie, Moussot, Mustapha, Benkhalifa, Rosalie, Cabry, Brigitte, Gubler, Hafida, Khorsi-Cauet, Moncef, Benkhalifa
منشور في 2022نص -
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Exome sequencing reveals a nonsense mutation in<i>TEX15</i>causing spermatogenic failure in a Turkish family حسب Özlem Okutman, Jean Muller, Yoni Baert, Münevver Serdarogullari, Meral Gültomruk, Amélie Piton, Charlotte Rombaut, Moncef Benkhalifa, Marius Teletin, Valerie Skory, Emre Bakırcıoğlu, Ellen Goossens, Mustafa Bahçeci, Stéphane Viville
منشور في 2015Artigo -
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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 حسب 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
منشور في 2017Artigo -
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Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots حسب Elias Elinati, Paul Kuentz, Claire Redin, Sara Jaber, Frauke Vanden Meerschaut, Joelle Makarian, Isabelle Koscinski, Mohammad Hossein Nasr‐Esfahani, Aygül Demi̇rol, Timur Gürgan, Noureddine Louanjli, Naeem Iqbal, Mazen Bisharah, F Pigeon, Hamid Gourabi, Dominique De Briel, Florence Brugnon, Susan Gitlin, Jean-Marc Grillo, Kamran Ghaedi, Mohammad Reza Deemeh, Somayeh Tanhaei, Parastoo Modarres, Björn Heindryckx, Moncef Benkhalifa, Dimitra Nikiforaki, Sergio Oehninger, Petra De Sutter, Jean Muller, Stéphane Viville
منشور في 2012Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Medicine
Infertility
Pregnancy
Andrology
Sperm
Gene
Male infertility
Internal medicine
Apoptosis
DNA
DNA fragmentation
Environmental health
Programmed cell death
Semen
Biochemistry
Chemistry
Fertility
Gynecology
Population
Semen analysis
Sperm motility
Antioxidant
Cell biology
Gene expression
Mutation
Physiology
Allele
Asthenozoospermia