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Thierry-Mieg

Showing results (81-90 of 128) with videos related to

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Clinical Genetics|November 17, 2023
CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humansFadwa Jreijiri, Emma Cavarocchi, Amir Amiri-Yekta, et al.
Andrology|January 9, 2025
A recurrent loss-of-function variant in DRC1 causes non-syndromic severe asthenozoospermia with favorable intracytoplasmic sperm injection and pregnancy outcomesCélia Tebbakh, Anne-Laure Barbotin, Guillaume Martinez, et al.
American Journal of Human Genetics|February 16, 2022
Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermiaZine-Eddine Kherraf, Caroline Cazin, Amine Bouker, et al.
AIDS (London, England)|May 13, 2006
Mortality and causes of death in adults receiving highly active antiretroviral therapy in Senegal: a 7-year cohort studyJean-François Etard, Ibrahima Ndiaye, Marion Thierry-Mieg, et al.
Human Reproduction (Oxford, England)|October 18, 2019
CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case reportJulie Beurois, Guillaume Martinez, Caroline Cazin, et al.
The EMBO Journal|August 3, 2017
Selective termination of lncRNA transcription promotes heterochromatin silencing and cell differentiationLeila Touat-Todeschini, Yuichi Shichino, Mathieu Dangin, et al.
Circulation Research|March 21, 2009
T cell-mediated inflammation in adipose tissue does not cause insulin resistance in hyperlipidemic miceAriane Sultan, Daniela Strodthoff, Anna-Karin Robertson, et al.
Cells|January 11, 2022
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 <i>C1orf185</i> and <i>CCT6B</i>Caroline Cazin, Yasmine Neirijnck, Corinne Loeuillet, et al.
Iscience|July 31, 2023
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humansEmma Cavarocchi, Camille Sayou, Patrick Lorès, et al.
International Journal of Molecular Sciences|March 6, 2021
Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North AfricaCaroline Cazin, Yasmine Boumerdassi, Guillaume Martinez, et al.
Pageof 13

Showing results (81-90 of 128) with videos related to

Sort By:
Pageof 13
Clinical Genetics|November 17, 2023
CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humansFadwa Jreijiri, Emma Cavarocchi, Amir Amiri-Yekta, et al.
Andrology|January 9, 2025
A recurrent loss-of-function variant in DRC1 causes non-syndromic severe asthenozoospermia with favorable intracytoplasmic sperm injection and pregnancy outcomesCélia Tebbakh, Anne-Laure Barbotin, Guillaume Martinez, et al.
American Journal of Human Genetics|February 16, 2022
Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermiaZine-Eddine Kherraf, Caroline Cazin, Amine Bouker, et al.
AIDS (London, England)|May 13, 2006
Mortality and causes of death in adults receiving highly active antiretroviral therapy in Senegal: a 7-year cohort studyJean-François Etard, Ibrahima Ndiaye, Marion Thierry-Mieg, et al.
Human Reproduction (Oxford, England)|October 18, 2019
CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case reportJulie Beurois, Guillaume Martinez, Caroline Cazin, et al.
The EMBO Journal|August 3, 2017
Selective termination of lncRNA transcription promotes heterochromatin silencing and cell differentiationLeila Touat-Todeschini, Yuichi Shichino, Mathieu Dangin, et al.
Circulation Research|March 21, 2009
T cell-mediated inflammation in adipose tissue does not cause insulin resistance in hyperlipidemic miceAriane Sultan, Daniela Strodthoff, Anna-Karin Robertson, et al.
Cells|January 11, 2022
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 <i>C1orf185</i> and <i>CCT6B</i>Caroline Cazin, Yasmine Neirijnck, Corinne Loeuillet, et al.
Iscience|July 31, 2023
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humansEmma Cavarocchi, Camille Sayou, Patrick Lorès, et al.
International Journal of Molecular Sciences|March 6, 2021
Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North AfricaCaroline Cazin, Yasmine Boumerdassi, Guillaume Martinez, et al.
Pageof 13