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Showing results (101-110 of 158) with videos related to

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Human Molecular Genetics|May 26, 2017
A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiencyCarolina Carlosama, Maëva Elzaiat, Liliana C Patiño, et al.
Journal of Medical Genetics|December 14, 2004
A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregationS Caburet, A Demarez, L Moumné, et al.
Human Genetics|June 7, 2020
DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformationMaëva Elzaiat, Delphine Flatters, Diana Carolina Sierra-Díaz, et al.
Human Molecular Genetics|December 26, 2007
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian developmentLara Moumné, Aurélie Dipietromaria, Frank Batista, et al.
Human Genetics|November 8, 2006
A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunctionJeyabalan Nallathambi, Lara Moumné, Elfride De Baere, et al.
Nucleic Acids Research|November 7, 2023
The forkhead DNA-binding domain binds specific G2-rich RNA sequencesCaroline Zutterling, Anne-Laure Todeschini, Deborah Fourmy, et al.
Cytogenetic and Genome Research|December 20, 2003
Structure, evolution and expression of the FOXL2 transcription unitJ Cocquet, E De Baere, M Gareil, et al.
Elife|November 5, 2014
The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cellsAdrien Georges, David L'Hôte, Anne Laure Todeschini, et al.
Human Molecular Genetics|November 18, 2008
Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress: evidence for a regulatory imbalance induced by disease-causing mutationsBérénice A Benayoun, Frank Batista, Jana Auer, et al.
Oncogene|July 17, 2012
Adult ovarian granulosa cell tumor transcriptomics: prevalence of FOXL2 target genes misregulation gives insights into the pathogenic mechanism of the p.Cys134Trp somatic mutationB A Benayoun, M Anttonen, D L'Hôte, et al.
Pageof 16

Showing results (101-110 of 158) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|May 26, 2017
A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiencyCarolina Carlosama, Maëva Elzaiat, Liliana C Patiño, et al.
Journal of Medical Genetics|December 14, 2004
A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregationS Caburet, A Demarez, L Moumné, et al.
Human Genetics|June 7, 2020
DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformationMaëva Elzaiat, Delphine Flatters, Diana Carolina Sierra-Díaz, et al.
Human Molecular Genetics|December 26, 2007
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian developmentLara Moumné, Aurélie Dipietromaria, Frank Batista, et al.
Human Genetics|November 8, 2006
A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunctionJeyabalan Nallathambi, Lara Moumné, Elfride De Baere, et al.
Nucleic Acids Research|November 7, 2023
The forkhead DNA-binding domain binds specific G2-rich RNA sequencesCaroline Zutterling, Anne-Laure Todeschini, Deborah Fourmy, et al.
Cytogenetic and Genome Research|December 20, 2003
Structure, evolution and expression of the FOXL2 transcription unitJ Cocquet, E De Baere, M Gareil, et al.
Elife|November 5, 2014
The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cellsAdrien Georges, David L'Hôte, Anne Laure Todeschini, et al.
Human Molecular Genetics|November 18, 2008
Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress: evidence for a regulatory imbalance induced by disease-causing mutationsBérénice A Benayoun, Frank Batista, Jana Auer, et al.
Oncogene|July 17, 2012
Adult ovarian granulosa cell tumor transcriptomics: prevalence of FOXL2 target genes misregulation gives insights into the pathogenic mechanism of the p.Cys134Trp somatic mutationB A Benayoun, M Anttonen, D L'Hôte, et al.
Pageof 16