Designing A Transgenic Chicken: Applying New Approaches Toward A Promising Bioreactor

Autor: Salahadin Bahrami, Amir Amiri-Yekta, Abbas Daneshipour, Seyedeh Hoda Jazayeri, Paul Edward Mozdziak, Mohammad Hossein Sanati, Hamid Gourabi

Publikováno v: Cell Journal, Vol 22, Iss 2, Pp 133-139 (2019)

Specific developmental characteristics of the chicken make it an attractive model for the generation of transgenic organisms. Chicken possess a strong potential for recombinant protein production and can be used as a powerful bioreactor to produce ph

Externí odkaz: https://doaj.org/article/643ef534c1d846aeaed5c43749018e24

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice

Autor: Feng Zhang, Yunxia Cao, Zine-Eddine Kherraf, Caroline Cazin, Chunyu Liu, Yuyan Zeng, Jiaxiong Wang, Amir Amiri-Yekta, Shenmin Yang, Seyedeh Hanieh Hosseini, Shuyan Tang, Pierre F. Ray, Yiling Zhou, Xiong Wang, Jiangshan Cong, Jinsong Li, Abbas Daneshipour, Lingbo Wang, Xiaojin He, Shixiong Tian, Li Jin

Publikováno v: Journal of Medical Genetics. 59:710-718

BackgroundOligoasthenoteratozoospermia is a typical feature of sperm malformations leading to male infertility. Only a few genes have been clearly identified as pathogenic genes of oligoasthenoteratozoospermia.Methods and resultsHere, we identified a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3f8cc50389b2bbc0338186af269e4a00
https://doi.org/10.1136/jmedgenet-2021-107919

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

Autor: Catherine Patrat, Patrick Lorès, Laurence Stouvenel, Marjorie Whitfield, Zine-Eddine Kherraf, Pierre F. Ray, Amir Amiri-Yekta, Raoudha Zouari, Caroline Cazin, Selima Fourati Ben Mustapha, Emma Cavarocchi, Christophe Arnoult, Seyedeh-Hanieh Hosseini, Aminata Touré, Marie-Astrid Llabador, Abbas Daneshipour, Lucile Ferreux, Charles Coutton, Nicolas Thierry-Mieg, Emmanuel Dulioust

Publikováno v: Human Genetics
Human Genetics, 2021, 140 (7), pp.1031-1043. ⟨10.1007/s00439-021-02270-7⟩
Human Genetics, Springer Verlag, 2021, 140 (7), pp.1031-1043. ⟨10.1007/s00439-021-02270-7⟩

International audience; Cilia and flagella are formed around an evolutionary conserved microtubule-based axoneme and are required for fluid and mucus clearance, tissue homeostasis, cell differentiation and movement. The formation and maintenance of c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5985f27ab7061d824c5749432dde7e2
https://hal.science/hal-03369854

Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility

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

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

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

Autor: Patrick Lorès, Zine-Eddine Kherraf, Amir Amiri-Yekta, Marjorie Whitfield, Abbas Daneshipour, Laurence Stouvenel, Caroline Cazin, Emma Cavarocchi, Charles Coutton, Marie-Astrid Llabador, Christophe Arnoult, Nicolas Thierry-Mieg, Lucile Ferreux, Catherine Patrat, Seyedeh-Hanieh Hosseini, Selima Fourati Ben Mustapha, Raoudha Zouari, Emmanuel Dulioust, Pierre F. Ray, Aminata Touré

Publikováno v: Human Genetics. 140:1045-1045

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e8518aa7c8729162a045803ca25b18ec
https://doi.org/10.1007/s00439-021-02278-z