Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Farid Abada"'
Autor:
Charles Coutton, Farid Abada, Thomas Karaouzene, Damien Sanlaville, Véronique Satre, Joël Lunardi, Pierre-Simon Jouk, Christophe Arnoult, Nicolas Thierry-Mieg, Pierre F Ray
Publikováno v:
PLoS Genetics, Vol 9, Iss 3, p e1003363 (2013)
We demonstrated previously that 75% of infertile men with round, acrosomeless spermatozoa (globozoospermia) had a homozygous 200-Kb deletion removing the totality of DPY19L2. We showed that this deletion occurred by Non-Allelic Homologous Recombinati
Externí odkaz:
https://doaj.org/article/dd74df991d9e4e61a2dd057e6ead14e7
Autor:
Catherine Poirot, François Vialard, Agnès Guichet, Jean Pierre Soulie, Florence Lestrade, Pierre-Simon Jouk, Christophe Arnoult, Joël Lunardi, Nathalie Rives, Pascale May-Panloup, Sylviane Hennebicq, Véronique Satre, Charles Coutton, Chema Triki, J. Rollet, Raoudha Zouari, Béatrice Dorphin, Ghaya Merdassi, Pierre F. Ray, Brigitte Benzacken, Farid Abada, Michael G. B. Blum, Isabelle Koscinski, Valérie Mitchell, Laeticia Hesters, Mariem Ben Khelifa, Radu Harbuz, Leila Keskes, Stéphane Viville
Publikováno v:
Human Reproduction
Human Reproduction, Oxford University Press (OUP), 2012, 27 (11), pp.3337-46. ⟨10.1093/humrep/des296⟩
Human Reproduction, 2012, 27 (11), pp.3337-46. ⟨10.1093/humrep/des296⟩
Human Reproduction, Oxford University Press (OUP), 2012, 27 (11), pp.3337-46. ⟨10.1093/humrep/des296⟩
Human Reproduction, 2012, 27 (11), pp.3337-46. ⟨10.1093/humrep/des296⟩
International audience; STUDY QUESTION: Can we identify new sequence variants in the aurora kinase C gene (AURKC) of patients with macrozoospermia and establish a genotype-phenotype correlation? SUMMARY ANSWER: We identified a new non-sense mutation,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a98931d93b88d52c124effbaff7e6a58
https://doi.org/10.1093/humrep/des296
https://doi.org/10.1093/humrep/des296
Autor:
Laetitia Hesters, Ghaya Merdassi, Denise Escalier, François Vialard, Mariem Ben Khelifa, Chema Triki, Farid Abada, Joël Lunardi, Charles Coutton, Florence Boitrelle, Véronique Satre, Rachel Levy, Pierre-Simon Jouk, Valérie Mitchell, Christophe Arnoult, Nathalie Sermondade, Sylviane Hennebicq, Pierre F. Ray, Raoudha Zouari
Publikováno v:
Human Reproduction. 27:2549-2558
STUDY QUESTION: Do DPY19L2 heterozygous deletions and point mutations account for some cases of globozoospermia? SUMMARY ANSWER: Two DPY19L2 heterozygous deletions and three point mutations were identified, thus further confirming that genetic altera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cce9385d75d818047337199e318fbdd
https://doi.org/10.1093/humrep/des160
https://doi.org/10.1093/humrep/des160
Autor:
Marrakchi Ouafi, Isabelle Koscinski, Ghaya Merdassi, B. Sèle, Fethi Zhioua, François Vialard, Stéphane Viville, Raoudha Zouari, Thérèse Schweitzer, Mariem Ben Khelifa, Radu Harbuz, Mounir Makni, Lazhar Halouani, Charles Coutton, Christophe Arnoult, Nathalie Sermondade, Pierre-Simon Jouk, Amel Zhioua, Virginie Pierre, Véronique Satre, Mahmoud Kharouf, Jessica Escoffier, Chema Triki, Yorgos Nikas, Pierre F. Ray, Habib Latrous, Sylviane Hennebicq, Joël Lunardi, Farid Abada
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2011, 88 (3), pp.351-61. ⟨10.1016/j.ajhg.2011.02.007⟩
American Journal of Human Genetics, 2011, 88 (3), pp.351-61. ⟨10.1016/j.ajhg.2011.02.007⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2011, 88 (3), pp.351-61. ⟨10.1016/j.ajhg.2011.02.007⟩
American Journal of Human Genetics, 2011, 88 (3), pp.351-61. ⟨10.1016/j.ajhg.2011.02.007⟩
International audience; An increasing number of couples require medical assistance to achieve a pregnancy, and more than 2% of the births in Western countries now result from assisted reproductive technologies. To identify genetic variants responsibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08cfa8e3ba7e594f43ef3353441c57a
https://doi.org/10.1016/j.ajhg.2011.02.007
https://doi.org/10.1016/j.ajhg.2011.02.007