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Showing results (141-150 of 158) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|September 8, 2016
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian InsufficiencyJustine Bouilly, Isabelle Beau, Sara Barraud, et al.
Cancer Research|November 21, 2022
The Oncogenic FOXL2 C134W Mutation Is a Key Driver of Granulosa Cell TumorsElena Llano, Anne Laure Todeschini, Natalia Felipe-Medina, et al.
The Journal of Pathology|March 19, 2008
FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)R Hersmus, N Kalfa, B de Leeuw, et al.
Plos One|March 20, 2012
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian FailureSandrine Caburet, Petra Zavadakova, Ziva Ben-Neriah, et al.
The New England Journal of Medicine|March 7, 2014
Mutant cohesin in premature ovarian failureSandrine Caburet, Valerie A Arboleda, Elena Llano, et al.
Human Mutation|August 29, 2015
Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1Frauke Coppieters, Anne Laure Todeschini, Takuro Fujimaki, et al.
Elife|December 13, 2017
A homozygous <i>FANCM</i> mutation underlies a familial case of non-syndromic primary ovarian insufficiencyBaptiste Fouquet, Patrycja Pawlikowska, Sandrine Caburet, et al.
Human Molecular Genetics|September 13, 2015
Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leadsAurélie Auguste, Laurianne Bessière, Anne-Laure Todeschini, et al.
Trends in Endocrinology and Metabolism: TEM|May 1, 2018
Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian InsufficiencyIlpo Huhtaniemi, Outi Hovatta, Antonio La Marca, et al.
European Journal of Endocrinology|April 29, 2006
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failurePaul Laissue, Sophie Christin-Maitre, Philippe Touraine, et al.
Pageof 16

Showing results (141-150 of 158) with videos related to

Sort By:
Pageof 16
The Journal of Clinical Endocrinology and Metabolism|September 8, 2016
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian InsufficiencyJustine Bouilly, Isabelle Beau, Sara Barraud, et al.
Cancer Research|November 21, 2022
The Oncogenic FOXL2 C134W Mutation Is a Key Driver of Granulosa Cell TumorsElena Llano, Anne Laure Todeschini, Natalia Felipe-Medina, et al.
The Journal of Pathology|March 19, 2008
FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)R Hersmus, N Kalfa, B de Leeuw, et al.
Plos One|March 20, 2012
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian FailureSandrine Caburet, Petra Zavadakova, Ziva Ben-Neriah, et al.
The New England Journal of Medicine|March 7, 2014
Mutant cohesin in premature ovarian failureSandrine Caburet, Valerie A Arboleda, Elena Llano, et al.
Human Mutation|August 29, 2015
Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1Frauke Coppieters, Anne Laure Todeschini, Takuro Fujimaki, et al.
Elife|December 13, 2017
A homozygous <i>FANCM</i> mutation underlies a familial case of non-syndromic primary ovarian insufficiencyBaptiste Fouquet, Patrycja Pawlikowska, Sandrine Caburet, et al.
Human Molecular Genetics|September 13, 2015
Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leadsAurélie Auguste, Laurianne Bessière, Anne-Laure Todeschini, et al.
Trends in Endocrinology and Metabolism: TEM|May 1, 2018
Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian InsufficiencyIlpo Huhtaniemi, Outi Hovatta, Antonio La Marca, et al.
European Journal of Endocrinology|April 29, 2006
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failurePaul Laissue, Sophie Christin-Maitre, Philippe Touraine, et al.
Pageof 16