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Showing results (221-230 of 247) with videos related to

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Science Advances|October 4, 2019
Ruminococcin C, a promising antibiotic produced by a human gut symbiontSteve Chiumento, Clarisse Roblin, Sylvie Kieffer-Jaquinod, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 2, 2016
Microduplication of the ARID1A gene causes intellectual disability with recognizable syndromic featuresMarie Bidart, Michèle El Atifi, Sarra Miladi, et al.
The EMBO Journal|June 3, 2020
NR2F1 regulates regional progenitor dynamics in the mouse neocortex and cortical gyrification in BBSOAS patientsMichele Bertacchi, Anna Lisa Romano, Agnès Loubat, et al.
Molecular Autism|April 7, 2015
Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorderAnne-Claude Tabet, Alain Verloes, Marion Pilorge, et al.
Ecology Letters|August 23, 2025
Understanding and Predicting Population Response to Anthropogenic Disturbance: Current Approaches and Novel OpportunitiesCassie N Speakman, Sarah Bull, Sarah Cubaynes, et al.
Annales De Genetique|July 18, 2002
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureI Luquet, F Mugneret, P D Athis, et al.
Molecular Psychiatry|September 16, 2015
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autismM Pilorge, C Fassier, H Le Corronc, et al.
Journal of Medical Genetics|March 9, 2017
<i>PBX1</i> haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humansPauline Le Tanno, Julie Breton, Marie Bidart, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 29, 2020
The unusual structure of Ruminococcin C1 antimicrobial peptide confers clinical propertiesClarisse Roblin, Steve Chiumento, Olivier Bornet, et al.
Journal of Medical Genetics|August 20, 2025
Resolving structural variations missed by short-read sequencing uncovers their pathogenicityCaroline Schluth-Bolard, Laïla El Khattabi, Pierre-Antoine Rollat-Farnier, et al.
Pageof 25

Showing results (221-230 of 247) with videos related to

Sort By:
Pageof 25
Science Advances|October 4, 2019
Ruminococcin C, a promising antibiotic produced by a human gut symbiontSteve Chiumento, Clarisse Roblin, Sylvie Kieffer-Jaquinod, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 2, 2016
Microduplication of the ARID1A gene causes intellectual disability with recognizable syndromic featuresMarie Bidart, Michèle El Atifi, Sarra Miladi, et al.
The EMBO Journal|June 3, 2020
NR2F1 regulates regional progenitor dynamics in the mouse neocortex and cortical gyrification in BBSOAS patientsMichele Bertacchi, Anna Lisa Romano, Agnès Loubat, et al.
Molecular Autism|April 7, 2015
Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorderAnne-Claude Tabet, Alain Verloes, Marion Pilorge, et al.
Ecology Letters|August 23, 2025
Understanding and Predicting Population Response to Anthropogenic Disturbance: Current Approaches and Novel OpportunitiesCassie N Speakman, Sarah Bull, Sarah Cubaynes, et al.
Annales De Genetique|July 18, 2002
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureI Luquet, F Mugneret, P D Athis, et al.
Molecular Psychiatry|September 16, 2015
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autismM Pilorge, C Fassier, H Le Corronc, et al.
Journal of Medical Genetics|March 9, 2017
<i>PBX1</i> haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humansPauline Le Tanno, Julie Breton, Marie Bidart, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 29, 2020
The unusual structure of Ruminococcin C1 antimicrobial peptide confers clinical propertiesClarisse Roblin, Steve Chiumento, Olivier Bornet, et al.
Journal of Medical Genetics|August 20, 2025
Resolving structural variations missed by short-read sequencing uncovers their pathogenicityCaroline Schluth-Bolard, Laïla El Khattabi, Pierre-Antoine Rollat-Farnier, et al.
Pageof 25