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Marc Fellous

Showing results (91-100 of 133) with videos related to

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Forensic Science International|January 11, 2005
Distribution of Y chromosome lineages in Jerba island populationHoussein Khodjet el Khil, Raja Triki Marrakchi, Besma Yacoubi Loueslati, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 27, 2012
Involvement of the ventral tegmental area in a rodent model of post-traumatic stress disorderNadia S Corral-Frias, Ryan P Lahood, Kimberly E Edelman-Vogelsang, et al.
Fertility and Sterility|April 14, 2007
Extinction of FOXL2 expression in aggressive ovarian granulosa cell tumors in childrenNicolas Kalfa, Pascal Philibert, Catherine Patte, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 18, 2003
Characterization of a putative type IV aminophospholipid transporter P-type ATPaseStéphane Flamant, Pascale Pescher, Brigitte Lemercier, et al.
European Journal of Endocrinology|January 2, 2008
Genetic investigation of four meiotic genes in women with premature ovarian failureBéatrice Mandon-Pépin, Philippe Touraine, Frédérique Kuttenn, et al.
The Journal of Urology|August 30, 2008
Aberrant expression of ovary determining gene FOXL2 in the testis and juvenile granulosa cell tumor in childrenNicolas Kalfa, Marc Fellous, Brigitte Boizet-Bonhoure, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|February 8, 2005
The transcription factor Sox9 is degraded by the ubiquitin-proteasome system and stabilized by a mutation in a ubiquitin-target siteHaruhiko Akiyama, Tetsu Kamitani, Xiaohong Yang, 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.
Frontiers in Computational Neuroscience|February 10, 2022
Editorial: Advances in Computational NeuroscienceThomas Nowotny, Sacha J van Albada, Jean-Marc Fellous, 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.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
Forensic Science International|January 11, 2005
Distribution of Y chromosome lineages in Jerba island populationHoussein Khodjet el Khil, Raja Triki Marrakchi, Besma Yacoubi Loueslati, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 27, 2012
Involvement of the ventral tegmental area in a rodent model of post-traumatic stress disorderNadia S Corral-Frias, Ryan P Lahood, Kimberly E Edelman-Vogelsang, et al.
Fertility and Sterility|April 14, 2007
Extinction of FOXL2 expression in aggressive ovarian granulosa cell tumors in childrenNicolas Kalfa, Pascal Philibert, Catherine Patte, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 18, 2003
Characterization of a putative type IV aminophospholipid transporter P-type ATPaseStéphane Flamant, Pascale Pescher, Brigitte Lemercier, et al.
European Journal of Endocrinology|January 2, 2008
Genetic investigation of four meiotic genes in women with premature ovarian failureBéatrice Mandon-Pépin, Philippe Touraine, Frédérique Kuttenn, et al.
The Journal of Urology|August 30, 2008
Aberrant expression of ovary determining gene FOXL2 in the testis and juvenile granulosa cell tumor in childrenNicolas Kalfa, Marc Fellous, Brigitte Boizet-Bonhoure, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|February 8, 2005
The transcription factor Sox9 is degraded by the ubiquitin-proteasome system and stabilized by a mutation in a ubiquitin-target siteHaruhiko Akiyama, Tetsu Kamitani, Xiaohong Yang, 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.
Frontiers in Computational Neuroscience|February 10, 2022
Editorial: Advances in Computational NeuroscienceThomas Nowotny, Sacha J van Albada, Jean-Marc Fellous, 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.
Pageof 14