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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 Tumour
Hager 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 silencing
Denis 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 telomeres
Thibaut 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 bodies
Adrien 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 Tumors
Laurianne 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 genes
Maria 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 breaks
Sandrine 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 deacetylase
Bérénice 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 development
Dorien Baetens, Hans Stoop, Frank Peelman, et al.
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Search research articles
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Showing results (21-30 of 38) with videos related to
Sort By:
Page
of 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 Tumour
Hager 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 silencing
Denis 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 telomeres
Thibaut 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 bodies
Adrien 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 Tumors
Laurianne 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 genes
Maria 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 breaks
Sandrine 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 deacetylase
Bérénice 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 development
Dorien Baetens, Hans Stoop, Frank Peelman, et al.
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of 4