Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Véronique Satre"'
Autor:
Yunxia Cao, Véronique Satre, Chunyu Liu, Charles Coutton, Qunshan Shen, Marjorie Whitfield, Kuokuo Li, Julie Beurois, Hongbin Liu, Xiaojin He, Dan Liang, Pierre F. Ray, Guillaume Martinez, Marie Bidart, Tristan Celse, Nicolas Thierry-Mieg, Huan Wu, Feng Zhang, Zine-Eddine Kherraf, Fangbiao Tao, Caroline Cazin, Christophe Arnoult, Mingrong Lv, Bing Song, Amir Amiri-Yekta, Aminata Touré
Publikováno v:
Human Genetics
Human Genetics, Springer Verlag, 2021, 140 (9), pp.1367-1377. ⟨10.1007/s00439-021-02313-z⟩
Human Genetics, 2021, 140 (9), pp.1367-1377. ⟨10.1007/s00439-021-02313-z⟩
Human Genetics, Springer Verlag, 2021, 140 (9), pp.1367-1377. ⟨10.1007/s00439-021-02313-z⟩
Human Genetics, 2021, 140 (9), pp.1367-1377. ⟨10.1007/s00439-021-02313-z⟩
International audience; Spermatozoa are polarized cells with a head and a flagellum joined together by the connecting piece. Flagellum integrity is critical for normal sperm function, and flagellum defects consistently lead to male infertility. Multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0056c77d0a1bd6fcea6d737f3474c0fd
https://hal.archives-ouvertes.fr/hal-03365264
https://hal.archives-ouvertes.fr/hal-03365264
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:
Guillaume, Martinez, Julie, Beurois, Denis, Dacheux, Caroline, Cazin, Marie, Bidart, Zine-Eddine, Kherraf, Derrick R, Robinson, Véronique, Satre, Gerald, Le Gac, Chandran, Ka, Isabelle, Gourlaouen, Yann, Fichou, Graciane, Petre, Emmanuel, Dulioust, Raoudha, Zouari, Nicolas, Thierry-Mieg, Aminata, Touré, Christophe, Arnoult, Mélanie, Bonhivers, Pierre, Ray, Charles, Coutton
Publikováno v:
Journal of medical genetics. 57(10)
Multiple morphological abnormalities of the flagella (MMAF) consistently lead to male infertility due to a reduced or absent sperm motility defined as asthenozoospermia. Despite numerous genes recently described to be recurrently associated with MMAF
Autor:
Marie Cristou-Kent, Nicolas Thierry-Mieg, Charles Coutton, Jessica Escoffier, Amir Amiri-Yekta, Xiaojin He, Sylviane Hennebicq, Mounir Makni, Mélanie Bonhivers, Nathalie Rives, Pierre F. Ray, Marie Bidart, Christophe Arnoult, H Gourabi, Raoudha Zouari, Seyedeh Hanieh Hosseini, Habib Latrous, Véronique Satre, Lazhar Halouani, Béatrice Conne, Mahmoud Kharouf, Aminata Touré, Magalie Boguenet, Guillaume Martinez, Feng Zhang, Zine-Eddine Kherraf, Ouafi Marrakchi, Serge Nef, Emmanuel Dulioust, Selima Fourati Ben Mustapha, Yunxia Cao, Antoine Saut, Karin Pernet-Gallay
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2019, 104 (2), pp.331-340. ⟨10.1016/j.ajhg.2018.12.013⟩
American Journal of Human Genetics, Vol. 104, No 2 (2019) pp. 331-340
American Journal of Human Genetics, 2019, 104 (2), pp.331-340. ⟨10.1016/j.ajhg.2018.12.013⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2019, 104 (2), pp.331-340. ⟨10.1016/j.ajhg.2018.12.013⟩
American Journal of Human Genetics, Vol. 104, No 2 (2019) pp. 331-340
American Journal of Human Genetics, 2019, 104 (2), pp.331-340. ⟨10.1016/j.ajhg.2018.12.013⟩
International audience; Male infertility is a major health concern. Among its different causes, multiple morphological abnormalities of the flagella (MMAF) induces asthenozoospermia and is one of the most severe forms of qualitative sperm defects. Sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e5d669797fe26252be6e26550d42b2b
https://hal.archives-ouvertes.fr/hal-02003335/document
https://hal.archives-ouvertes.fr/hal-02003335/document
Autor:
Mahmoud Kharouf, Pierre F. Ray, Guillaume Martinez, Ouafi Marrakchi, Véronique Satre, Raoudha Zouari, Habib Latrous, Clémentine Wambergue, Lazhar Halouani, Françoise Devillard, Sophie Brouillet, Mounir Makni, Charles Coutton, Christophe Arnoult, Sylviane Hennebicq, Selima Fourati Ben Mustapha, Florence Amblard
Publikováno v:
Human Reproduction. 31:1164-1172
STUDY QUESTION Does DNAH1 status influence intracytoplasmic sperm injection (ICSI) outcomes for patients with multiple morphological abnormalities of the sperm flagella (MMAF)? SUMMARY ANSWER Despite a highly abnormal morphology, sperm from MMAF pati
Autor:
Thomas Karaouzène, Seyedeh Hanieh Hosseini, Nicolas Thierry-Mieg, Emmanuel Dulioust, Laurence Stouvenel, Pierre F. Ray, Abbas Daneshipour, Aminata Touré, Frederick N. Dong, Véronique Satre, Mélanie Bonhivers, Patrick Lorès, Amir Amiri-Yekta, Haiqing Zhao, Christophe Arnoult, Julie Tek, Antoine Saut, Hamid Gourabi, Guillaume Martinez, Sophie Brouillet, Charles Coutton
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2018, 102 (4), pp.636-648. ⟨10.1016/j.ajhg.2018.03.007⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2018, 102 (4), pp.636-648. ⟨10.1016/j.ajhg.2018.03.007⟩
The multiple morphological abnormalities of the flagella (MMAF) phenotype is among the most severe forms of sperm defects responsible for male infertility. The phenotype is characterized by the presence in the ejaculate of immotile spermatozoa with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::febb9c33ed17186e55f0459638c7d614
https://hal.archives-ouvertes.fr/hal-01877985
https://hal.archives-ouvertes.fr/hal-01877985
Autor:
Mahmoud Kharouf, Guillaume Martinez, Jessica Escoffier, Denis Dacheux, Alain Schmitt, Raoudha Zouari, Zine-Eddine Kherraf, Pierre-Simon Jouk, Mélanie Bonhivers, Lazhar Halouani, Julien Fauré, Anne Boland, Elma El Khouri, Valérie Mitchell, Nicolas Thierry-Mieg, Emmanuel Dulioust, Serge P. Bottari, Serge Nef, Karin Pernet-Gallay, Jean-François Deleuze, Amir Amiri-Yekta, Habib Latrous, Patrick Lorès, Hamid Gourabi, Pauline Le Tanno, Nicolas Landrein, Thomas Karaouzène, Selima Fourati Ben Mustapha, Aminata Touré, Alexandra Vargas, Derrick R. Robinson, Véronique Satre, Ouafi Marrakchi, Béatrice Conne, Serge Crouzy, Seyedeh Hanieh Hosseini, Mounir Makni, Laurence Stouvenel, Clémentine Wambergue-Legrand, Abbas Daneshipour, Charles Coutton, Pierre F. Ray, Sylviane Hennebicq, Christophe Arnoult, Jean-Philippe Wolf
Publikováno v:
Nature Communications
Nature Communications, 2018, 9, pp.686. ⟨10.1038/s41467-017-02792-7⟩
Nature Communications, Vol 9, Iss 1, Pp 1-18 (2018)
Nature Communications, Nature Publishing Group, 2018, 9, pp.686. ⟨10.1038/s41467-017-02792-7⟩
Nature Communications, Vol. 9, No 1 (2018) P. 686
Nature Communications, 2018, 9, pp.686. ⟨10.1038/s41467-017-02792-7⟩
Nature Communications, Vol 9, Iss 1, Pp 1-18 (2018)
Nature Communications, Nature Publishing Group, 2018, 9, pp.686. ⟨10.1038/s41467-017-02792-7⟩
Nature Communications, Vol. 9, No 1 (2018) P. 686
Spermatogenesis defects concern millions of men worldwide, yet the vast majority remains undiagnosed. Here we report men with primary infertility due to multiple morphological abnormalities of the sperm flagella with severe disorganization of the spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::131014d2865f04abad4e856b758bd5d6
https://hal.science/hal-01724640
https://hal.science/hal-01724640
Autor:
Mélanie Bonhivers, Nicolas Thierry-Mieg, Amir Amiri-Yekta, Thomas Karaouzène, Raoudha Zouari, Marie Bidart, Charles Coutton, Véronique Satre, Mahmoud Kharouf, Aminata Touré, Pierre F. Ray, Karin Pernet-Gallay, Guillaume Martinez, Jean-Pascal Hograindleur, Antoine Saut, Denis Dacheux-Deschamps, Anne Bertrand, Zine-Eddine Kherraf, Christophe Arnoult, Selima Fourati Ben Mustapha
Publikováno v:
Human Reproduction
Human Reproduction, Oxford University Press (OUP), 2018, 33 (10), pp.1973-1984. ⟨10.1093/humrep/dey264⟩
Human Reproduction, Oxford University Press (OUP), 2018, 33 (10), pp.1973-1984. ⟨10.1093/humrep/dey264⟩
Study question Can whole-exome sequencing (WES) of infertile patients identify new genes responsible for multiple morphological abnormalities of the sperm flagella (MMAF)? Summary answer WES analysis of 78 infertile men with a MMAF phenotype permitte
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,
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