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Farah Ghieh

Showing results (1-10 of 11) with videos related to

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Basic and Clinical Andrology|April 27, 2019
Genetic defects in human azoospermiaFarah Ghieh, Valérie Mitchell, Béatrice Mandon-Pepin, et al.
Basic and Clinical Andrology|April 22, 2021
Human testis-expressed (TEX) genes: a review focused on spermatogenesis and male fertilityHela Bellil, Farah Ghieh, Emeline Hermel, et al.
Genes|September 28, 2023
Mammal Reproductive Homeobox (Rhox) Genes: An Update of Their Involvement in Reproduction and DevelopmentMorgane Le Beulze, Cécile Daubech, Aissatu Balde-Camara, et al.
Basic and Clinical Andrology|August 19, 2021
Will whole-genome sequencing become the first-line genetic analysis for male infertility in the near future?Farah Ghieh, Anne-Laure Barbotin, Clara Leroy, et al.
Andrologia|September 14, 2022
Cryptic splice site poisoning and meiotic arrest caused by a homozygous frameshift mutation in RBMXL2: A case reportFarah Ghieh, Vincent Izard, Marine Poulain, et al.
Asian Journal of Andrology|February 8, 2023
ZMYM3 : a new candidate gene in nonobstructive azoospermia?Morgane Le Beulze, Nelly Swierkowski-Blanchard, Farah Ghieh, et al.
Genes|November 27, 2021
DYRK1A Overexpression in Mice Downregulates the Gonadotropic Axis and Disturbs Early Stages of SpermatogenesisRodolphe Dard, Manon Moreau, Estelle Parizot, et al.
Basic and Clinical Andrology|November 11, 2021
Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?Farah Ghieh, Anne-Laure Barbotin, Julie Prasivoravong, et al.
Plos One|September 4, 2024
A partial deletion within the meiosis-specific sporulation domain SPO22 of Tex11 is not associated with infertility in miceFarah Ghieh, Bruno Passet, Elodie Poumerol, et al.
Molecular Human Reproduction|July 8, 2020
STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermiaSylvie Jaillard, Kenneth McElreavy, Gorjana Robevska, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Basic and Clinical Andrology|April 27, 2019
Genetic defects in human azoospermiaFarah Ghieh, Valérie Mitchell, Béatrice Mandon-Pepin, et al.
Basic and Clinical Andrology|April 22, 2021
Human testis-expressed (TEX) genes: a review focused on spermatogenesis and male fertilityHela Bellil, Farah Ghieh, Emeline Hermel, et al.
Genes|September 28, 2023
Mammal Reproductive Homeobox (Rhox) Genes: An Update of Their Involvement in Reproduction and DevelopmentMorgane Le Beulze, Cécile Daubech, Aissatu Balde-Camara, et al.
Basic and Clinical Andrology|August 19, 2021
Will whole-genome sequencing become the first-line genetic analysis for male infertility in the near future?Farah Ghieh, Anne-Laure Barbotin, Clara Leroy, et al.
Andrologia|September 14, 2022
Cryptic splice site poisoning and meiotic arrest caused by a homozygous frameshift mutation in RBMXL2: A case reportFarah Ghieh, Vincent Izard, Marine Poulain, et al.
Asian Journal of Andrology|February 8, 2023
ZMYM3 : a new candidate gene in nonobstructive azoospermia?Morgane Le Beulze, Nelly Swierkowski-Blanchard, Farah Ghieh, et al.
Genes|November 27, 2021
DYRK1A Overexpression in Mice Downregulates the Gonadotropic Axis and Disturbs Early Stages of SpermatogenesisRodolphe Dard, Manon Moreau, Estelle Parizot, et al.
Basic and Clinical Andrology|November 11, 2021
Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?Farah Ghieh, Anne-Laure Barbotin, Julie Prasivoravong, et al.
Plos One|September 4, 2024
A partial deletion within the meiosis-specific sporulation domain SPO22 of Tex11 is not associated with infertility in miceFarah Ghieh, Bruno Passet, Elodie Poumerol, et al.
Molecular Human Reproduction|July 8, 2020
STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermiaSylvie Jaillard, Kenneth McElreavy, Gorjana Robevska, et al.
Pageof 2