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Showing results (131-140 of 158) with videos related to

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Journal of Medical Genetics|May 12, 2009
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2P Laissue, B Lakhal, B A Benayoun, 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.
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.
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.
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.
Human Mutation|May 20, 2008
Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patientsJeyabalan Nallathambi, Paul Laissue, Frank Batista, et al.
Human Molecular Genetics|March 11, 2014
STAG3 is a strong candidate gene for male infertilityElena Llano, Laura Gomez-H, Ignacio García-Tuñón, 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 Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysisRachel A Ruotolo, Nestor A Veitia, Aaron Corbin, et al.
Pageof 16

Showing results (131-140 of 158) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|May 12, 2009
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2P Laissue, B Lakhal, B A Benayoun, 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.
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.
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.
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.
Human Mutation|May 20, 2008
Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patientsJeyabalan Nallathambi, Paul Laissue, Frank Batista, et al.
Human Molecular Genetics|March 11, 2014
STAG3 is a strong candidate gene for male infertilityElena Llano, Laura Gomez-H, Ignacio García-Tuñón, 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 Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysisRachel A Ruotolo, Nestor A Veitia, Aaron Corbin, et al.
Pageof 16