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Showing results (151-160 of 158) with videos related to

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Open Biology|November 3, 2016
Association of FOXD1 variants with adverse pregnancy outcomes in mice and humansPaul Laissue, Besma Lakhal, Magalie Vatin, et al.
Elife|August 27, 2020
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1Natalia Felipe-Medina, Sandrine Caburet, Fernando Sánchez-Sáez, et al.
Human Mutation|March 17, 2010
FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletionsB D'haene, J Nevado, M Pugeat, et al.
Cell Death and Differentiation|May 27, 2022
A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functionsMonica M Franca, Yazmine B Condezo, Maëva Elzaiat, et al.
Nature|April 25, 2014
Superconducting quantum circuits at the surface code threshold for fault toleranceR Barends, J Kelly, A Megrant, et al.
American Journal of Human Genetics|June 18, 2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndromeD Beysen, J Raes, B P Leroy, et al.
Human Mutation|July 22, 2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndromeDiane Beysen, Sarah De Jaegere, David Amor, et al.
Genome Biology|March 31, 2012
The transcription factor encyclopediaDimas Yusuf, Stefanie L Butland, Magdalena I Swanson, et al.
Pageof 16

Showing results (151-160 of 158) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 158 results.
Open Biology|November 3, 2016
Association of FOXD1 variants with adverse pregnancy outcomes in mice and humansPaul Laissue, Besma Lakhal, Magalie Vatin, et al.
Elife|August 27, 2020
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1Natalia Felipe-Medina, Sandrine Caburet, Fernando Sánchez-Sáez, et al.
Human Mutation|March 17, 2010
FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletionsB D'haene, J Nevado, M Pugeat, et al.
Cell Death and Differentiation|May 27, 2022
A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functionsMonica M Franca, Yazmine B Condezo, Maëva Elzaiat, et al.
Nature|April 25, 2014
Superconducting quantum circuits at the surface code threshold for fault toleranceR Barends, J Kelly, A Megrant, et al.
American Journal of Human Genetics|June 18, 2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndromeD Beysen, J Raes, B P Leroy, et al.
Human Mutation|July 22, 2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndromeDiane Beysen, Sarah De Jaegere, David Amor, et al.
Genome Biology|March 31, 2012
The transcription factor encyclopediaDimas Yusuf, Stefanie L Butland, Magdalena I Swanson, et al.
Pageof 16