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Anne-Laure Todeschini

Showing results (21-30 of 38) with videos related to

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Journal of Clinical Research in Pediatric Endocrinology|April 14, 2021
Precocious Pseudo-puberty in a Two-year-old Girl, Presenting with Bilateral Ovarian Enlargement and Progressing to Unilateral Juvenile Granulosa Cell TumourHager Barakizou, Souha Gannouni, Thouraya Kamoun, et al.
Plos One|May 14, 2014
The Drosophila Su(var)3-7 gene is required for oogenesis and female fertility, genetically interacts with piwi and aubergine, but impacts only weakly transposon silencingDenis Basquin, Anne Spierer, Flora Begeot, et al.
Plos One|September 25, 2008
Telomeric trans-silencing in Drosophila melanogaster: tissue specificity, development and functional interactions between non-homologous telomeresThibaut Josse, Corinne Maurel-Zaffran, Augustin de Vanssay, et al.
Plos One|October 25, 2011
SUMOylation of the Forkhead transcription factor FOXL2 promotes its stabilization/activation through transient recruitment to PML bodiesAdrien Georges, Bérénice A Benayoun, Mara Marongiu, et al.
Ebiomedicine|July 3, 2015
A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell TumorsLaurianne Bessière, Anne-Laure Todeschini, Aurélie Auguste, et al.
Clinical Genetics|July 3, 2020
An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genesMaria Isabel Alvarez-Mora, Anne-Laure Todeschini, Sandrine Caburet, et al.
The Journal of Pathology|August 2, 2021
FOXL2 in adult-type granulosa cell tumour of the ovary: oncogene or tumour suppressor gene?Jessica A Pilsworth, Anne-Laure Todeschini, Samantha J Neilson, et al.
Ebiomedicine|April 20, 2019
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaksSandrine Caburet, Anne-Laure Todeschini, Cynthia Petrillo, et al.
Human Molecular Genetics|February 4, 2011
Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylaseBérénice A Benayoun, Adrien B Georges, David L'Hôte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 5, 2016
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex developmentDorien Baetens, Hans Stoop, Frank Peelman, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Journal of Clinical Research in Pediatric Endocrinology|April 14, 2021
Precocious Pseudo-puberty in a Two-year-old Girl, Presenting with Bilateral Ovarian Enlargement and Progressing to Unilateral Juvenile Granulosa Cell TumourHager Barakizou, Souha Gannouni, Thouraya Kamoun, et al.
Plos One|May 14, 2014
The Drosophila Su(var)3-7 gene is required for oogenesis and female fertility, genetically interacts with piwi and aubergine, but impacts only weakly transposon silencingDenis Basquin, Anne Spierer, Flora Begeot, et al.
Plos One|September 25, 2008
Telomeric trans-silencing in Drosophila melanogaster: tissue specificity, development and functional interactions between non-homologous telomeresThibaut Josse, Corinne Maurel-Zaffran, Augustin de Vanssay, et al.
Plos One|October 25, 2011
SUMOylation of the Forkhead transcription factor FOXL2 promotes its stabilization/activation through transient recruitment to PML bodiesAdrien Georges, Bérénice A Benayoun, Mara Marongiu, et al.
Ebiomedicine|July 3, 2015
A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell TumorsLaurianne Bessière, Anne-Laure Todeschini, Aurélie Auguste, et al.
Clinical Genetics|July 3, 2020
An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genesMaria Isabel Alvarez-Mora, Anne-Laure Todeschini, Sandrine Caburet, et al.
The Journal of Pathology|August 2, 2021
FOXL2 in adult-type granulosa cell tumour of the ovary: oncogene or tumour suppressor gene?Jessica A Pilsworth, Anne-Laure Todeschini, Samantha J Neilson, et al.
Ebiomedicine|April 20, 2019
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaksSandrine Caburet, Anne-Laure Todeschini, Cynthia Petrillo, et al.
Human Molecular Genetics|February 4, 2011
Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylaseBérénice A Benayoun, Adrien B Georges, David L'Hôte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 5, 2016
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex developmentDorien Baetens, Hans Stoop, Frank Peelman, et al.
Pageof 4