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Anne-Laure Todeschini

Showing results (31-40 of 38) with videos related to

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Human Molecular Genetics|June 3, 2011
Mutational probing of the forkhead domain of the transcription factor FOXL2 provides insights into the pathogenicity of naturally occurring mutationsAnne-Laure Todeschini, Aurélie Dipietromaria, David L'hôte, et al.
Nucleic Acids Research|March 2, 2012
Tye7 regulates yeast Ty1 retrotransposon sense and antisense transcription in response to adenylic nucleotides stressGéraldine Servant, Benoit Pinson, Aurélie Tchalikian-Cosson, et al.
Plos One|January 26, 2010
Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G)Bérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, et al.
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.
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.
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.
Elife|August 27, 2020
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1Natalia Felipe-Medina, Sandrine Caburet, Fernando Sánchez-Sáez, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Human Molecular Genetics|June 3, 2011
Mutational probing of the forkhead domain of the transcription factor FOXL2 provides insights into the pathogenicity of naturally occurring mutationsAnne-Laure Todeschini, Aurélie Dipietromaria, David L'hôte, et al.
Nucleic Acids Research|March 2, 2012
Tye7 regulates yeast Ty1 retrotransposon sense and antisense transcription in response to adenylic nucleotides stressGéraldine Servant, Benoit Pinson, Aurélie Tchalikian-Cosson, et al.
Plos One|January 26, 2010
Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G)Bérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, et al.
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.
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.
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.
Elife|August 27, 2020
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1Natalia Felipe-Medina, Sandrine Caburet, Fernando Sánchez-Sáez, et al.
Pageof 4