Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Chema Triki"'
Autor:
Alicia Coudert, Caroline Cazin, Amir Amiri-Yekta, Selima Fourati Ben Mustapha, Raoudha Zouari, Julien Bessonat, Abdelali Zoghmar, Antoine Clergeau, Catherine Metzler-Guillemain, Chema Triki, Hervé Lejeune, Nathalie Sermondade, Eva Pipiras, Nadia Prisant, Isabelle Cedrin, Isabelle Koscinski, Leila Keskes, Florence Lestrade, Laetitia Hesters, Nathalie Rives, Béatrice Dorphin, Agnes Guichet, Catherine Patrat, Emmanuel Dulioust, Aurélie Feraille, François Robert, Sophie Brouillet, Frédéric Morel, Aurore Perrin, Nathalie Rougier, Eric Bieth, Arthur Sorlin, Jean-Pierre Siffroi, Mariem Ben Khelifa, Florence Boiterelle, Sylvianne Hennebicq, Veronique Satre, Christophe Arnoult, Charles Coutton, Anne-Laure Barbotin, Nicolas Thierry-Mieg, Zine-Eddine Kherraf, Pierre F. Ray
Publikováno v:
Journal of Genetics and Genomics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::696e334e821c19551adbf0d6f3bf42b6
https://doi.org/10.1016/j.jgg.2023.04.007
https://doi.org/10.1016/j.jgg.2023.04.007
Autor:
Ségolène Veau, Gilles Schuler, Aline Papaxanthos, Julien Bessonnat, Marine Poulain, H. Lejeune, Laurent Pasquier, Rosalie Cabry, Raoudha Zouari, Amandine Septier, Flore Mietton, Myriam Chaabouni, Vincent Achard, Zine-Eddine Kherraf, Charles Coutton, Antoine Clergeau, Dominique Lauton, Christophe Sifer, Béatrice Dorphin, Catherine Guillemain, Mahmoud Kharouf, Tristan Celse, Sebti Benbouhadja, Nathalie Sermondade, Selima Fourati Ben Mustapha, Pierre F. Ray, Delphine Martinez, Bernard Foliguet, Julie Beurois, Valérie Mitchell, Guillaume Martinez, Abdelali Zoghmar, Véronique Satre, Ahmed Chargui, Gérard Tachdjian, Cynthia Frapsauce, Chema Triki, Sylviane Hennebicq, Jacques Puechberty, Caroline Cazin, Christophe Arnoult, Nicolas Thierry-Mieg, Lionel Mery
Publikováno v:
Human Genetics
Human Genetics, Springer Verlag, 2021, Molecular Genetics of Male Infertility, 140 (1), pp.43-57. ⟨10.1007/s00439-020-02229-0⟩
Human Genetics, Springer Verlag, In press, ⟨10.1007/s00439-020-02229-0⟩
Human Genetics, 2021, Molecular Genetics of Male Infertility, 140 (1), pp.43-57. ⟨10.1007/s00439-020-02229-0⟩
Human Genetics, Springer Verlag, 2021, Molecular Genetics of Male Infertility, 140 (1), pp.43-57. ⟨10.1007/s00439-020-02229-0⟩
Human Genetics, Springer Verlag, In press, ⟨10.1007/s00439-020-02229-0⟩
Human Genetics, 2021, Molecular Genetics of Male Infertility, 140 (1), pp.43-57. ⟨10.1007/s00439-020-02229-0⟩
International audience; Globozoospermia is a rare phenotype of primary male infertility inducing the production of round-headed spermatozoa without acrosome. Anomalies of DPY19L2 account for 50-70% of all cases and the entire deletion of the gene is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f529143440a28307c54a227d5849354
https://hal.archives-ouvertes.fr/hal-03025179
https://hal.archives-ouvertes.fr/hal-03025179
Autor:
Raoudha Zouari, Nicolas Thierry-Mieg, Thomas Karaouzène, Zine Eddine Kherraf, Hoi Chang Lee, Lazhar Halouani, Serge Nef, Charles Coutton, Christophe Arnoult, Rafael A. Fissore, Chema Triki, Jessica Escoffier, Sergey N. Savinov, Guillaume Martinez, Sandra Yassine, Pierre F. Ray
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (5), pp.878-891. ⟨10.1093/hmg/ddv617⟩
Human Molecular Genetics, Vol. 25, No 5 (2016) pp. 878-891
Human Molecular Genetics, 2016, 25 (5), pp.878-891. ⟨10.1093/hmg/ddv617⟩
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (5), pp.878-891. ⟨10.1093/hmg/ddv617⟩
Human Molecular Genetics, Vol. 25, No 5 (2016) pp. 878-891
Human Molecular Genetics, 2016, 25 (5), pp.878-891. ⟨10.1093/hmg/ddv617⟩
International audience; In mammals, sperm-oocyte fusion initiates Ca(2+) oscillations leading to a series of events called oocyte activation, which is the first stage of embryo development. Ca(2+) signaling is elicited by the delivery of an oocyte-ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4473bb9d687d112b0304e3ad32aaf4c4
https://hal.archives-ouvertes.fr/hal-01877966
https://hal.archives-ouvertes.fr/hal-01877966
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