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Clinical Endocrinology
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July 15, 2017
A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations
Francoise Paris, Delphine Flatters, Sandrine Caburet, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 14, 2008
Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy
Boomiraj Hemadevi, Reiner A Veitia, Muthiah Srinivasan, et al.
Molecular and Cellular Endocrinology
|
December 25, 2007
The mutations and potential targets of the forkhead transcription factor FOXL2
L Moumné, F Batista, B A Benayoun, et al.
BMC Cancer
|
April 18, 2015
Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes
Sandrine Caburet, Mikko Anttonen, Anne-Laure Todeschini, et al.
Clinical Genetics
|
January 16, 2016
A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency
F Fauchereau, S Shalev, E Chervinsky, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
February 24, 2020
The Gene Balance Hypothesis: Epigenetics and Dosage Effects in Plants
Xiaowen Shi, Chen Chen, Hua Yang, et al.
Human Molecular Genetics
|
May 1, 2012
Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological roles
David L'Hôte, Adrien Georges, Anne Laure Todeschini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 10, 2012
Dynamics of the subcellular localization of RalBP1/RLIP through the cell cycle: the role of targeting signals and of protein-protein interactions
Jonathan Fillatre, Delphine Delacour, Lucie Van Hove, 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 insufficiency
Kamal Bouhali, Aurélie Dipietromaria, Anastasia Fontaine, et al.
Human Molecular Genetics
|
July 19, 2008
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles
Bérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, et al.
Page
of 16
Search research articles
Search
Showing results (111-120 of 158) with videos related to
Sort By:
Page
of 16
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 simulations
Francoise Paris, Delphine Flatters, Sandrine Caburet, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 14, 2008
Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy
Boomiraj Hemadevi, Reiner A Veitia, Muthiah Srinivasan, et al.
Molecular and Cellular Endocrinology
|
December 25, 2007
The mutations and potential targets of the forkhead transcription factor FOXL2
L Moumné, F Batista, B A Benayoun, et al.
BMC Cancer
|
April 18, 2015
Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes
Sandrine Caburet, Mikko Anttonen, Anne-Laure Todeschini, et al.
Clinical Genetics
|
January 16, 2016
A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency
F Fauchereau, S Shalev, E Chervinsky, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
February 24, 2020
The Gene Balance Hypothesis: Epigenetics and Dosage Effects in Plants
Xiaowen Shi, Chen Chen, Hua Yang, et al.
Human Molecular Genetics
|
May 1, 2012
Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological roles
David L'Hôte, Adrien Georges, Anne Laure Todeschini, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 10, 2012
Dynamics of the subcellular localization of RalBP1/RLIP through the cell cycle: the role of targeting signals and of protein-protein interactions
Jonathan Fillatre, Delphine Delacour, Lucie Van Hove, 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 insufficiency
Kamal Bouhali, Aurélie Dipietromaria, Anastasia Fontaine, et al.
Human Molecular Genetics
|
July 19, 2008
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles
Bérénice A Benayoun, Sandrine Caburet, Aurélie Dipietromaria, et al.
Page
of 16