Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Veitia

Showing results (111-120 of 158) with videos related to

Pageof 16
Sort By:
Clinical Endocrinology|July 15, 2017
A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulationsFrancoise Paris, Delphine Flatters, Sandrine Caburet, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 14, 2008
Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophyBoomiraj Hemadevi, Reiner A Veitia, Muthiah Srinivasan, et al.
Molecular and Cellular Endocrinology|December 25, 2007
The mutations and potential targets of the forkhead transcription factor FOXL2L Moumné, F Batista, B A Benayoun, et al.
BMC Cancer|April 18, 2015
Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genesSandrine Caburet, Mikko Anttonen, Anne-Laure Todeschini, et al.
Clinical Genetics|January 16, 2016
A non-sense MCM9 mutation in a familial case of primary ovarian insufficiencyF Fauchereau, S Shalev, E Chervinsky, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 24, 2020
The Gene Balance Hypothesis: Epigenetics and Dosage Effects in PlantsXiaowen Shi, Chen Chen, Hua Yang, et al.
Human Molecular Genetics|May 1, 2012
Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological rolesDavid L'Hôte, Adrien Georges, Anne Laure Todeschini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 10, 2012
Dynamics of the subcellular localization of RalBP1/RLIP through the cell cycle: the role of targeting signals and of protein-protein interactionsJonathan Fillatre, Delphine Delacour, Lucie Van Hove, et al.
Human Molecular Genetics|April 21, 2011
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiencyKamal Bouhali, Aurélie Dipietromaria, Anastasia Fontaine, et al.
Human Molecular Genetics|July 19, 2008
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant allelesBérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, et al.
Pageof 16

Showing results (111-120 of 158) with videos related to

Sort By:
Pageof 16
Clinical Endocrinology|July 15, 2017
A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulationsFrancoise Paris, Delphine Flatters, Sandrine Caburet, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 14, 2008
Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophyBoomiraj Hemadevi, Reiner A Veitia, Muthiah Srinivasan, et al.
Molecular and Cellular Endocrinology|December 25, 2007
The mutations and potential targets of the forkhead transcription factor FOXL2L Moumné, F Batista, B A Benayoun, et al.
BMC Cancer|April 18, 2015
Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genesSandrine Caburet, Mikko Anttonen, Anne-Laure Todeschini, et al.
Clinical Genetics|January 16, 2016
A non-sense MCM9 mutation in a familial case of primary ovarian insufficiencyF Fauchereau, S Shalev, E Chervinsky, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 24, 2020
The Gene Balance Hypothesis: Epigenetics and Dosage Effects in PlantsXiaowen Shi, Chen Chen, Hua Yang, et al.
Human Molecular Genetics|May 1, 2012
Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological rolesDavid L'Hôte, Adrien Georges, Anne Laure Todeschini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 10, 2012
Dynamics of the subcellular localization of RalBP1/RLIP through the cell cycle: the role of targeting signals and of protein-protein interactionsJonathan Fillatre, Delphine Delacour, Lucie Van Hove, et al.
Human Molecular Genetics|April 21, 2011
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiencyKamal Bouhali, Aurélie Dipietromaria, Anastasia Fontaine, et al.
Human Molecular Genetics|July 19, 2008
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant allelesBérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, et al.
Pageof 16