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Sandrine Caburet

Showing results (11-20 of 32) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 19, 2009
Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?Adrien B Georges, Bérénice A Benayoun, Sandrine Caburet, et al.
Genome Research|July 19, 2005
Human ribosomal RNA gene arrays display a broad range of palindromic structuresSandrine Caburet, Chiara Conti, Catherine Schurra, et al.
European Journal of Endocrinology|March 29, 2017
A homozygous mutation of <i>GNRHR</i> in a familial case diagnosed with polycystic ovary syndromeSandrine Caburet, Ronit Beck Fruchter, Bérangère Legois, et al.
Molecular and Cellular Endocrinology|July 19, 2011
The transcription factor FOXL2: at the crossroads of ovarian physiology and pathologySandrine Caburet, Adrien Georges, David L'Hôte, et al.
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.
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.
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.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2020
Conventional and unconventional interactions of the transcription factor FOXL2 uncovered by a proteome-wide analysisMay Penrad-Mobayed, Caroline Perrin, Laetitia Herman, 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.
Pediatric Endocrinology Reviews : PER|October 7, 2005
Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunctionElfride De Baere, Silvia Copelli, Sandrine Caburet, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 19, 2009
Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?Adrien B Georges, Bérénice A Benayoun, Sandrine Caburet, et al.
Genome Research|July 19, 2005
Human ribosomal RNA gene arrays display a broad range of palindromic structuresSandrine Caburet, Chiara Conti, Catherine Schurra, et al.
European Journal of Endocrinology|March 29, 2017
A homozygous mutation of <i>GNRHR</i> in a familial case diagnosed with polycystic ovary syndromeSandrine Caburet, Ronit Beck Fruchter, Bérangère Legois, et al.
Molecular and Cellular Endocrinology|July 19, 2011
The transcription factor FOXL2: at the crossroads of ovarian physiology and pathologySandrine Caburet, Adrien Georges, David L'Hôte, et al.
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.
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.
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.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2020
Conventional and unconventional interactions of the transcription factor FOXL2 uncovered by a proteome-wide analysisMay Penrad-Mobayed, Caroline Perrin, Laetitia Herman, 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.
Pediatric Endocrinology Reviews : PER|October 7, 2005
Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunctionElfride De Baere, Silvia Copelli, Sandrine Caburet, et al.
Pageof 4