Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella
Ben Khelifa, Mariem, Coutton, Charles, Zouari, Raoudha, Karaouzène, Thomas, Rendu, John, Bidart, Marie, Yassine, Sandra, Pierre, Virginie, Delaroche, Julie, Hennebicq, Sylviane, Grunwald, Didier, Escalier, Denise, Pernet-Gallay, Karine, Jouk, Pierre-Simon, Thierry-Mieg, Nicolas, Touré, Aminata, Arnoult, Christophe, Ray, Pierre F.
Published in American journal of human genetics (02.01.2014)
Published in American journal of human genetics (02.01.2014)
Get full text
Journal Article
Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice
Liu, Wangjie, He, Xiaojin, Yang, Shenmin, Zouari, Raoudha, Wang, Jiaxiong, Wu, Huan, Kherraf, Zine-Eddine, Liu, Chunyu, Coutton, Charles, Zhao, Rui, Tang, Dongdong, Tang, Shuyan, Lv, Mingrong, Fang, Youyan, Li, Weiyu, Li, Hong, Zhao, Jianyuan, Wang, Xue, Zhao, Shimin, Zhang, Jingjing, Arnoult, Christophe, Jin, Li, Zhang, Zhiguo, Ray, Pierre F., Cao, Yunxia, Zhang, Feng
Published in American journal of human genetics (04.04.2019)
Published in American journal of human genetics (04.04.2019)
Get full text
Journal Article
A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility
Kherraf, Zine-Eddine, Amiri-Yekta, Amir, Dacheux, Denis, Karaouzène, Thomas, Coutton, Charles, Christou-Kent, Marie, Martinez, Guillaume, Landrein, Nicolas, Le Tanno, Pauline, Fourati Ben Mustapha, Selima, Halouani, Lazhar, Marrakchi, Ouafi, Makni, Mounir, Latrous, Habib, Kharouf, Mahmoud, Pernet-Gallay, Karin, Gourabi, Hamid, Robinson, Derrick R., Crouzy, Serge, Blum, Michael, Thierry-Mieg, Nicolas, Touré, Aminata, Zouari, Raoudha, Arnoult, Christophe, Bonhivers, Mélanie, Ray, Pierre F.
Published in American journal of human genetics (06.09.2018)
Published in American journal of human genetics (06.09.2018)
Get full text
Journal Article
Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility
Lorès, Patrick, Dacheux, Denis, Kherraf, Zine-Eddine, Nsota Mbango, Jean-Fabrice, Coutton, Charles, Stouvenel, Laurence, Ialy-Radio, Come, Amiri-Yekta, Amir, Whitfield, Marjorie, Schmitt, Alain, Cazin, Caroline, Givelet, Maëlle, Ferreux, Lucile, Fourati Ben Mustapha, Selima, Halouani, Lazhar, Marrakchi, Ouafi, Daneshipour, Abbas, El Khouri, Elma, Do Cruzeiro, Marcio, Favier, Maryline, Guillonneau, François, Chaudhry, Marhaba, Sakheli, Zeinab, Wolf, Jean-Philippe, Patrat, Catherine, Gacon, Gérard, Savinov, Sergey N., Hosseini, Seyedeh Hanieh, Robinson, Derrick R., Zouari, Raoudha, Ziyyat, Ahmed, Arnoult, Christophe, Dulioust, Emmanuel, Bonhivers, Mélanie, Ray, Pierre F., Touré, Aminata
Published in American journal of human genetics (05.12.2019)
Published in American journal of human genetics (05.12.2019)
Get full text
Journal Article
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome
Lorès, Patrick, Kherraf, Zine-Eddine, Amiri-Yekta, Amir, Whitfield, Marjorie, Daneshipour, Abbas, Stouvenel, Laurence, Cazin, Caroline, Cavarocchi, Emma, Coutton, Charles, Llabador, Marie-Astrid, Arnoult, Christophe, Thierry-Mieg, Nicolas, Ferreux, Lucile, Patrat, Catherine, Hosseini, Seyedeh-Hanieh, Mustapha, Selima Fourati Ben, Zouari, Raoudha, Dulioust, Emmanuel, Ray, Pierre F., Touré, Aminata
Published in Human genetics (01.07.2021)
Published in Human genetics (01.07.2021)
Get full text
Journal Article
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Christou‐Kent, Marie, Kherraf, Zine‐Eddine, Amiri‐Yekta, Amir, Le Blévec, Emilie, Karaouzène, Thomas, Conne, Béatrice, Escoffier, Jessica, Assou, Said, Guttin, Audrey, Lambert, Emeline, Martinez, Guillaume, Boguenet, Magalie, Fourati Ben Mustapha, Selima, Cedrin Durnerin, Isabelle, Halouani, Lazhar, Marrakchi, Ouafi, Makni, Mounir, Latrous, Habib, Kharouf, Mahmoud, Coutton, Charles, Thierry‐Mieg, Nicolas, Nef, Serge, Bottari, Serge P, Zouari, Raoudha, Issartel, Jean Paul, Ray, Pierre F, Arnoult, Christophe
Published in EMBO molecular medicine (01.05.2018)
Published in EMBO molecular medicine (01.05.2018)
Get full text
Journal Article
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation
Harbuz, Radu, Zouari, Raoudha, Pierre, Virginie, Ben Khelifa, Mariem, Kharouf, Mahmoud, Coutton, Charles, Merdassi, Ghaya, Abada, Farid, Escoffier, Jessica, Nikas, Yorgos, Vialard, François, Koscinski, Isabelle, Triki, Chema, Sermondade, Nathalie, Schweitzer, Thérèse, Zhioua, Amel, Zhioua, Fethi, Latrous, Habib, Halouani, Lazhar, Ouafi, Marrakchi, Makni, Mounir, Jouk, Pierre-Simon, Sèle, Bernard, Hennebicq, Sylviane, Satre, Véronique, Viville, Stéphane, Arnoult, Christophe, Lunardi, Joël, Ray, Pierre F.
Published in American journal of human genetics (11.03.2011)
Published in American journal of human genetics (11.03.2011)
Get full text
Journal Article
Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function
Dacheux, Denis, Martinez, Guillaume, Broster Reix, Christine E, Beurois, Julie, Lores, Patrick, Tounkara, Magamba, Dupuy, Jean-William, Robinson, Derrick Roy, Loeuillet, Corinne, Lambert, Emeline, Wehbe, Zeina, Escoffier, Jessica, Amiri-Yekta, Amir, Daneshipour, Abbas, Hosseini, Seyedeh-Hanieh, Zouari, Raoudha, Mustapha, Selima Fourati Ben, Halouani, Lazhar, Jiang, Xiaohui, Shen, Ying, Liu, Chunyu, Thierry-Mieg, Nicolas, Septier, Amandine, Bidart, Marie, Satre, Véronique, Cazin, Caroline, Kherraf, Zine Eddine, Arnoult, Christophe, Ray, Pierre F, Toure, Aminata, Bonhivers, Mélanie, Coutton, Charles
Published in eLife (07.11.2023)
Published in eLife (07.11.2023)
Get full text
Journal Article
Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse
Muroňová, Jana, Kherraf, Zine Eddine, Giordani, Elsa, Lambert, Emeline, Eckert, Simon, Cazin, Caroline, Amiri-Yekta, Amir, Court, Magali, Chevalier, Geneviève, Martinez, Guillaume, Neirijnck, Yasmine, Kühne, Francoise, Wehrli, Lydia, Klena, Nikolai, Hamel, Virginie, De Macedo, Lisa, Escoffier, Jessica, Guichard, Paul, Coutton, Charles, Mustapha, Selima Fourati Ben, Kharouf, Mahmoud, Bouin, Anne-Pacale, Zouari, Raoudha, Thierry-Mieg, Nicolas, Nef, Serge, Geimer, Stefan, Loeuillet, Corinne, Ray, Pierre F, Arnoult, Christophe
Published in eLife (05.03.2024)
Published in eLife (05.03.2024)
Get full text
Journal Article
Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa
Cazin, Caroline, Boumerdassi, Yasmine, Martinez, Guillaume, Fourati Ben Mustapha, Selima, Whitfield, Marjorie, Coutton, Charles, Thierry-Mieg, Nicolas, Di Pizio, Pierre, Rives, Nathalie, Arnoult, Christophe, Touré, Aminata, Ray, Pierre F, Zouari, Raoudha, Sifer, Christophe, Kherraf, Zine-Eddine
Published in International journal of molecular sciences (22.02.2021)
Published in International journal of molecular sciences (22.02.2021)
Get full text
Journal Article
Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome
Lorès, Patrick, Kherraf, Zine-Eddine, Amiri-Yekta, Amir, Whitfield, Marjorie, Daneshipour, Abbas, Stouvenel, Laurence, Cazin, Caroline, Cavarocchi, Emma, Coutton, Charles, Llabador, Marie-Astrid, Arnoult, Christophe, Thierry-Mieg, Nicolas, Ferreux, Lucile, Patrat, Catherine, Hosseini, Seyedeh-Hanieh, Mustapha, Selima Fourati Ben, Zouari, Raoudha, Dulioust, Emmanuel, Ray, Pierre F., Touré, Aminata
Published in Human genetics (01.07.2021)
Published in Human genetics (01.07.2021)
Get full text
Journal Article
Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B
Cazin, Caroline, Neirijnck, Yasmine, Loeuillet, Corinne, Wehrli, Lydia, Kühne, Françoise, Lordey, Isabelle, Mustapha, Selima Fourati Ben, Bouker, Amin, Zouari, Raoudha, Thierry-Mieg, Nicolas, Nef, Serge, Arnoult, Christophe, Ray, Pierre F, Kherraf, Zine-Eddine
Published in Cells (Basel, Switzerland) (01.01.2022)
Published in Cells (Basel, Switzerland) (01.01.2022)
Get full text
Journal Article
Lebestatin, a disintegrin from Macrovipera venom, inhibits integrin-mediated cell adhesion, migration and angiogenesis
OLFA, Kallech-Ziri, JOSE, Luis, JEAN-MARC, Sabatier, MOHAMED, El Ayeb, NAZIHA, Marrakchi, SALMA, Daoud, AMINE, Bazaa, SRAIRI ABID NAJET, NICOLAS, Andreotti, MAXIME, Lehmann, RAOUDHA, Zouari, KAMEL, Mabrouk, JACQUES, Marvaldi
Published in Laboratory investigation (01.12.2005)
Published in Laboratory investigation (01.12.2005)
Get full text
Journal Article
MVL-PLA2, a snake venom phospholipase A2, inhibits angiogenesis through an increase in microtubule dynamics and disorganization of focal adhesions
Bazaa, Amine, Pasquier, Eddy, Defilles, Céline, Limam, Ines, Kessentini-Zouari, Raoudha, Kallech-Ziri, Olfa, El Battari, Assou, Braguer, Diane, El Ayeb, Mohamed, Marrakchi, Naziha, Luis, José
Published in PloS one (12.04.2010)
Published in PloS one (12.04.2010)
Get full text
Journal Article
Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia
Kherraf, Zine-Eddine, Cazin, Caroline, Bouker, Amine, Fourati Ben Mustapha, Selima, Hennebicq, Sylviane, Septier, Amandine, Coutton, Charles, Raymond, Laure, Nouchy, Marc, Thierry-Mieg, Nicolas, Zouari, Raoudha, Arnoult, Christophe, Ray, Pierre F.
Published in American journal of human genetics (03.03.2022)
Published in American journal of human genetics (03.03.2022)
Get full text
Journal Article
CFAP61 is required for sperm flagellum formation and male fertility in human and mouse
Liu, Siyu, Zhang, Jintao, Kherraf, Zine Eddine, Sun, Shuya, Zhang, Xin, Cazin, Caroline, Coutton, Charles, Zouari, Raoudha, Zhao, Shuqin, Hu, Fan, Fourati Ben Mustapha, Selima, Arnoult, Christophe, Ray, Pierre F, Liu, Mingxi
Published in Development (Cambridge) (01.12.2021)
Published in Development (Cambridge) (01.12.2021)
Get full text
Journal Article
Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella
Martinez, Guillaume, Kherraf, Zine-Eddine, Zouari, Raoudha, Fourati Ben Mustapha, Selima, Saut, Antoine, Pernet-Gallay, Karin, Bertrand, Anne, Bidart, Marie, Hograindleur, Jean Pascal, Amiri-Yekta, Amir, Kharouf, Mahmoud, Karaouzène, Thomas, Thierry-Mieg, Nicolas, Dacheux-Deschamps, Denis, Satre, Véronique, Bonhivers, Mélanie, Touré, Aminata, Arnoult, Christophe, Ray, Pierre F, Coutton, Charles
Published in Human reproduction (Oxford) (01.10.2018)
Published in Human reproduction (Oxford) (01.10.2018)
Get full text
Journal Article
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human
Coutton, Charles, Vargas, Alexandra S., Amiri-Yekta, Amir, Kherraf, Zine-Eddine, Ben Mustapha, Selima Fourati, Le Tanno, Pauline, Wambergue-Legrand, Clémentine, Karaouzène, Thomas, Martinez, Guillaume, Crouzy, Serge, Daneshipour, Abbas, Hosseini, Seyedeh Hanieh, Mitchell, Valérie, Halouani, Lazhar, Marrakchi, Ouafi, Makni, Mounir, Latrous, Habib, Kharouf, Mahmoud, Deleuze, Jean-François, Boland, Anne, Hennebicq, Sylviane, Satre, Véronique, Jouk, Pierre-Simon, Thierry-Mieg, Nicolas, Conne, Beatrice, Dacheux, Denis, Landrein, Nicolas, Schmitt, Alain, Stouvenel, Laurence, Lorès, Patrick, El Khouri, Elma, Bottari, Serge P., Fauré, Julien, Wolf, Jean-Philippe, Pernet-Gallay, Karin, Escoffier, Jessica, Gourabi, Hamid, Robinson, Derrick R., Nef, Serge, Dulioust, Emmanuel, Zouari, Raoudha, Bonhivers, Mélanie, Touré, Aminata, Arnoult, Christophe, Ray, Pierre F.
Published in Nature communications (15.02.2018)
Published in Nature communications (15.02.2018)
Get full text
Journal Article
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP
Escoffier, Jessica, Lee, Hoi Chang, Yassine, Sandra, Zouari, Raoudha, Martinez, Guillaume, Karaouzène, Thomas, Coutton, Charles, Kherraf, Zine-Eddine, Halouani, Lazhar, Triki, Chema, Nef, Serge, Thierry-Mieg, Nicolas, Savinov, Sergey N, Fissore, Rafael, Ray, Pierre F, Arnoult, Christophe
Published in Human molecular genetics (01.03.2016)
Published in Human molecular genetics (01.03.2016)
Get full text
Journal Article
Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice
Coutton, Charles, Martinez, Guillaume, Kherraf, Zine-Eddine, Amiri-Yekta, Amir, Boguenet, Magalie, Saut, Antoine, He, Xiaojin, Zhang, Feng, Cristou-Kent, Marie, Escoffier, Jessica, Bidart, Marie, Satre, Véronique, Conne, Béatrice, Fourati Ben Mustapha, Selima, Halouani, Lazhar, Marrakchi, Ouafi, Makni, Mounir, Latrous, Habib, Kharouf, Mahmoud, Pernet-Gallay, Karin, Bonhivers, Mélanie, Hennebicq, Sylviane, Rives, Nathalie, Dulioust, Emmanuel, Touré, Aminata, Gourabi, Hamid, Cao, Yunxia, Zouari, Raoudha, Hosseini, Seyedeh Hanieh, Nef, Serge, Thierry-Mieg, Nicolas, Arnoult, Christophe, Ray, Pierre F.
Published in American journal of human genetics (07.02.2019)
Published in American journal of human genetics (07.02.2019)
Get full text
Journal Article