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Emmanuel Dulioust

Showing results (11-20 of 25) with videos related to

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The Journal of Antimicrobial Chemotherapy|September 30, 2017
Penetration and antiviral efficacy of total and unbound maraviroc, raltegravir and rilpivirine in both female and male genital fluids from HIV-positive patients receiving regimens containing these antiretroviralsMinh P Lê, Linda Belarbi, Marie-Laure Chaix, et al.
Human Reproduction (Oxford, England)|September 16, 2021
Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellumLucile Ferreux, Mathilde Bourdon, Ahmed Chargui, et al.
Clinical Genetics|January 19, 2021
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertilityEmma Cavarocchi, Marjorie Whitfield, Ahmed Chargui, et al.
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.
American Journal of Human Genetics|April 16, 2013
Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermiaThassadite Dirami, Baptiste Rode, Mathilde Jollivet, 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.
American Journal of Human Genetics|April 3, 2018
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and MouseFrederick N Dong, Amir Amiri-Yekta, Guillaume Martinez, et al.
Journal of Medical Genetics|March 13, 2020
Biallelic variants in <i>MAATS1</i> encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertilityGuillaume Martinez, Julie Beurois, Denis Dacheux, et al.
Human Genetics|March 10, 2021
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 syndromePatrick Lorès, Zine-Eddine Kherraf, Amir Amiri-Yekta, et al.
American Journal of Human Genetics|July 4, 2020
Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male InfertilityChunyu Liu, Haruhiko Miyata, Yang Gao, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

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Pageof 3
The Journal of Antimicrobial Chemotherapy|September 30, 2017
Penetration and antiviral efficacy of total and unbound maraviroc, raltegravir and rilpivirine in both female and male genital fluids from HIV-positive patients receiving regimens containing these antiretroviralsMinh P Lê, Linda Belarbi, Marie-Laure Chaix, et al.
Human Reproduction (Oxford, England)|September 16, 2021
Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellumLucile Ferreux, Mathilde Bourdon, Ahmed Chargui, et al.
Clinical Genetics|January 19, 2021
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertilityEmma Cavarocchi, Marjorie Whitfield, Ahmed Chargui, et al.
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.
American Journal of Human Genetics|April 16, 2013
Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermiaThassadite Dirami, Baptiste Rode, Mathilde Jollivet, 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.
American Journal of Human Genetics|April 3, 2018
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and MouseFrederick N Dong, Amir Amiri-Yekta, Guillaume Martinez, et al.
Journal of Medical Genetics|March 13, 2020
Biallelic variants in <i>MAATS1</i> encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertilityGuillaume Martinez, Julie Beurois, Denis Dacheux, et al.
Human Genetics|March 10, 2021
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 syndromePatrick Lorès, Zine-Eddine Kherraf, Amir Amiri-Yekta, et al.
American Journal of Human Genetics|July 4, 2020
Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male InfertilityChunyu Liu, Haruhiko Miyata, Yang Gao, et al.
Pageof 3