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Valérie Mitchell

Showing results (21-30 of 31) with videos related to

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American Journal of Human Genetics|August 2, 2016
Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas DeferensOlivier Patat, Adrien Pagin, Aurore Siegfried, et al.
Journal of Visualized Experiments : Jove|April 22, 2014
Consensus brain-derived protein, extraction protocol for the study of human and murine brain proteome using both 2D-DIGE and mini 2DE immunoblottingFrancisco-Jose Fernandez-Gomez, Fanny Jumeau, Maxime Derisbourg, et al.
Human Reproduction (Oxford, England)|May 26, 2012
MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermiaCharles Coutton, Raoudha Zouari, Farid Abada, et al.
Reproductive Biomedicine Online|September 24, 2023
Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopyAngèle Boursier, Augustin Boudry, Valérie Mitchell, et al.
American Journal of Human Genetics|November 6, 2012
Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesiaEsther Kott, Philippe Duquesnoy, Bruno Copin, et al.
American Journal of Human Genetics|June 11, 2019
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to AsthenozoospermiaMarjorie Whitfield, Lucie Thomas, Emilie Bequignon, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2022
Defining Reference Ranges for Serum Anti-Müllerian Hormone on a Large Cohort of Normozoospermic Adult Men Highlights New Potential Physiological Functions of AMH on FSH Secretion and Sperm MotilityHamza Benderradji, Anne-Laure Barbotin, Maryse Leroy-Billiard, et al.
Human Reproduction (Oxford, England)|August 14, 2012
Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermiaMariem Ben Khelifa, Charles Coutton, Michael G B Blum, et al.
American Journal of Human Genetics|January 25, 2020
TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus FlagellaLucie Thomas, Khaled Bouhouche, Marjorie Whitfield, et al.
Human Genetics|October 27, 2020
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest playerTristan Celse, Caroline Cazin, Flore Mietton, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|August 2, 2016
Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas DeferensOlivier Patat, Adrien Pagin, Aurore Siegfried, et al.
Journal of Visualized Experiments : Jove|April 22, 2014
Consensus brain-derived protein, extraction protocol for the study of human and murine brain proteome using both 2D-DIGE and mini 2DE immunoblottingFrancisco-Jose Fernandez-Gomez, Fanny Jumeau, Maxime Derisbourg, et al.
Human Reproduction (Oxford, England)|May 26, 2012
MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermiaCharles Coutton, Raoudha Zouari, Farid Abada, et al.
Reproductive Biomedicine Online|September 24, 2023
Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopyAngèle Boursier, Augustin Boudry, Valérie Mitchell, et al.
American Journal of Human Genetics|November 6, 2012
Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesiaEsther Kott, Philippe Duquesnoy, Bruno Copin, et al.
American Journal of Human Genetics|June 11, 2019
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to AsthenozoospermiaMarjorie Whitfield, Lucie Thomas, Emilie Bequignon, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2022
Defining Reference Ranges for Serum Anti-Müllerian Hormone on a Large Cohort of Normozoospermic Adult Men Highlights New Potential Physiological Functions of AMH on FSH Secretion and Sperm MotilityHamza Benderradji, Anne-Laure Barbotin, Maryse Leroy-Billiard, et al.
Human Reproduction (Oxford, England)|August 14, 2012
Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermiaMariem Ben Khelifa, Charles Coutton, Michael G B Blum, et al.
American Journal of Human Genetics|January 25, 2020
TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus FlagellaLucie Thomas, Khaled Bouhouche, Marjorie Whitfield, et al.
Human Genetics|October 27, 2020
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest playerTristan Celse, Caroline Cazin, Flore Mietton, et al.
Pageof 4