Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Caroline Cazin"'
Autor:
Zine-Eddine, Kherraf, Caroline, Cazin, Florence, Lestrade, Jana, Muronova, Charles, Coutton, Christophe, Arnoult, Nicolas, Thierry-Mieg, Pierre F, Ray
Publikováno v:
Asian journal of andrology. 24(3)
Thanks to tremendous advances in sequencing technologies and in particular to whole exome sequencing (WES), many genes have now been linked to severe sperm defects. A precise genetic diagnosis is obtained for a minority of patients and only for the m
Autor:
M. Dhellemmes, Magalie Boguenet, Yasmine Neirijnck, J. Muronova, Zine-Eddine Kherraf, Guillaume Martinez, G. Chevalier, Emeline Lambert, Jessica Escoffier, Serge Nef, Charles Coutton, Caroline Cazin, C. Vilpreux, Christophe Arnoult, C. Loeuillet, Jean-Pascal Hograindleur, Pierre F. Ray
Publikováno v:
eLife
eLife, 2022, 11, pp.e75373. ⟨10.7554/eLife.75373⟩
eLife, 2022, 11, pp.e75373. ⟨10.7554/eLife.75373⟩
Male infertility is an important health concern that is expected to have a major genetic etiology. Although high-throughput sequencing has linked gene defects to more than 50% of rare and severe sperm anomalies, less than 20% of common and moderate f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e4a48985b4c2af2c2e7f3f81088f437
https://doi.org/10.1101/2021.11.15.468601
https://doi.org/10.1101/2021.11.15.468601
Autor:
Caroline Cazin, Pierre F. Ray, Christophe Arnoult, Seyedeh Hanieh Hosseini, Amir Amiri-Yekta, Nicolas Thierry-Mieg, Selima Fourati Ben Mustapha, Zine-Eddine Kherraf, Raoudha Zouari, Magalie Boguenet, Aminata Touré, Mahmoud Kharouf, Guillaume Martinez, Charles Coutton, Hamid Gourabi, Abbas Daneshipour
Publikováno v:
Clinical Genetics
Clinical Genetics, Wiley, 2019, 96 (5), pp.394-401. ⟨10.1111/cge.13604⟩
Clinical Genetics, Wiley, 2019, 96 (5), pp.394-401. ⟨10.1111/cge.13604⟩
Multiple morphological anomalies of the sperm flagella (MMAF syndrome) is a severe male infertility phenotype which has so far been formally linked to the presence of biallelic mutations in nine genes mainly coding for axonemal proteins overexpressed
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:
Soheila Sarmadi, Maryam Varkiani, Amir Amiri-Yekta, Navid Almadani, Alireza Biglari, Niloofar Sodeifi, Tina Shahani, Caroline Cazin, Fariba Ramezanali, Pierre F. Ray, Mehdi Totonchi, Hamid Gourabi, Nayeralsadat Fatemi, Zine-Eddine Kherraf
Publikováno v:
European journal of obstetrics, gynecology, and reproductive biology. 259
Objective Recurrent pregnancy loss (RPL) is a common infertility-related complication that affects approximately 1–3 % of women worldwide. Known causes of etiology are found in approximately half the cases but the other half remain unexplained. It
Autor:
Pierre F. Ray, Guillaume Martinez, Charles Coutton, Zine-Eddine Kherraf, Julie Beurois, Caroline Cazin, Christophe Arnoult, Aminata Touré
Publikováno v:
Human Genetics
Human Genetics, Springer Verlag, 2020, ⟨10.1007/s00439-020-02113-x⟩
Human Genetics, Springer Verlag, 2020, ⟨10.1007/s00439-020-02113-x⟩
Spermatozoa contain highly specialized structural features reflecting unique functions required for fertilization. Among them, the flagellum is a sperm-specific organelle required to generate the motility, which is essential to reach the egg. The fla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bfc2a24c613f1436ad105eaa8dede8c
https://hal-cnrs.archives-ouvertes.fr/hal-03004953
https://hal-cnrs.archives-ouvertes.fr/hal-03004953
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:
Marhaba Chaudhry, Sergey N. Savinov, Caroline Cazin, Gérard Gacon, Laurence Stouvenel, Abbas Daneshipour, Christophe Arnoult, Jean-Philippe Wolf, François Guillonneau, Raoudha Zouari, Pierre F. Ray, Maëlle Givelet, Jean-Fabrice Nsota Mbango, Alain Schmitt, Emmanuel Dulioust, Amir Amiri-Yekta, Lazhar Halouani, Denis Dacheux, Zeinab Sakheli, Patrick Lorès, Selima Fourati Ben Mustapha, Côme Ialy-Radio, Charles Coutton, Seyedeh Hanieh Hosseini, Aminata Touré, Lucile Ferreux, Maryline Favier, Mélanie Bonhivers, Zine-Eddine Kherraf, Catherine Patrat, Derrick R. Robinson, Ahmed Ziyyat, Ouafi Marrakchi, Elma El Khouri, Marjorie Whitfield, Marcio Do Cruzeiro
Publikováno v:
The American Journal of Human Genetics
The American Journal of Human Genetics, 2019, ⟨10.1016/j.ajhg.2019.10.007⟩
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2019, ⟨10.1016/j.ajhg.2019.10.007⟩
American Journal of Human Genetics, 2019, ⟨10.1016/j.ajhg.2019.10.007⟩
Am J Hum Genet
The American Journal of Human Genetics, 2019, ⟨10.1016/j.ajhg.2019.10.007⟩
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2019, ⟨10.1016/j.ajhg.2019.10.007⟩
American Journal of Human Genetics, 2019, ⟨10.1016/j.ajhg.2019.10.007⟩
Am J Hum Genet
International audience; In humans, structural or functional defects of the sperm flagellum induce asthenozoospermia, which accounts for the main sperm defect encountered in infertile men. Herein we focused on morphological abnormalities of the sperm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4224e59804c9a276dfc1f4bcadeecdab
https://hal.archives-ouvertes.fr/hal-02370384
https://hal.archives-ouvertes.fr/hal-02370384
Autor:
Weiyu, Li, Huan, Wu, Fuping, Li, Shixiong, Tian, Zine-Eddine, Kherraf, Jintao, Zhang, Xiaoqing, Ni, Mingrong, Lv, Chunyu, Liu, Qing, Tan, Ying, Shen, Amir, Amiri-Yekta, Caroline, Cazin, Jingjing, Zhang, Wangjie, Liu, Yan, Zheng, Huiru, Cheng, Yingbi, Wu, Jiajia, Wang, Yang, Gao, Yujie, Chen, Xiaomin, Zha, Li, Jin, Mingxi, Liu, Xiaojin, He, Pierre F, Ray, Yunxia, Cao, Feng, Zhang
Publikováno v:
Journal of medical genetics. 57(2)
Male infertility is a prevalent issue worldwide, mostly due to the impaired sperm motility. Multiple morphological abnormalities of the sperm flagella (MMAF) present aberrant spermatozoa with absent, short, coiled, bent and irregular-calibre flagella
Autor:
Julie Beurois, Marie Bidart, Véronique Satre, Aminata Touré, Nicolas Thierry-Mieg, Graciane Petre, Amir Amiri-Yekta, Pierre F. Ray, Sophie Brouillet, Zine-Eddine Kherraf, Charles Coutton, Guillaume Martinez, Caroline Cazin, Christophe Arnoult
Publikováno v:
Human reproduction (Oxford, England). 34(10)
The use of high-throughput sequencing techniques has allowed the identification of numerous mutations in genes responsible for severe astheno-teratozoospermia due to multiple morphological abnormalities of the sperm flagella (MMAF). However, more tha