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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 humans
Fadwa 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 outcomes
Célia 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 azoospermia
Zine-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 study
Jean-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 report
Julie Beurois, Guillaume Martinez, Caroline Cazin, et al.
The EMBO Journal
|
August 3, 2017
Selective termination of lncRNA transcription promotes heterochromatin silencing and cell differentiation
Leila 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 mice
Ariane 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 humans
Emma 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 Africa
Caroline Cazin, Yasmine Boumerdassi, Guillaume Martinez, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 128) with videos related to
Sort By:
Page
of 13
Clinical Genetics
|
November 17, 2023
CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans
Fadwa 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 outcomes
Célia 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 azoospermia
Zine-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 study
Jean-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 report
Julie Beurois, Guillaume Martinez, Caroline Cazin, et al.
The EMBO Journal
|
August 3, 2017
Selective termination of lncRNA transcription promotes heterochromatin silencing and cell differentiation
Leila 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 mice
Ariane 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 humans
Emma 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 Africa
Caroline Cazin, Yasmine Boumerdassi, Guillaume Martinez, et al.
Page
of 13