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Pierre Blanc

Showing results (121-130 of 147) with videos related to

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Human Genetics|February 7, 2025
Unilateral, bilateral symmetric or asymmetric isolated hearing loss in patients with heterozygous KITLG variantsMargaux Serey-Gaut, Ralyath Balogoun, Laurence Jonard, et al.
Cell Host & Microbe|September 18, 2021
Genomic and functional characterization of a mucosal symbiont involved in early-stage colorectal cancerMelissa C Kordahi, Ian B Stanaway, Marion Avril, et al.
Genome Research|April 4, 2008
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repairMarijke Bauters, Hilde Van Esch, Michael J Friez, et al.
Gastroenterology|February 26, 2026
Uncovering the dynamics of mucosa-associated microbiota in post-operative recurrence of Crohn's diseaseLéonard Dubois, Alexandre Chaussard, Philippe Seksik, et al.
Journal of Medical Genetics|September 17, 2025
Heterozygous alterations of <i>GTF2I</i> at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorderJeanne Jury, Thomas Besnard, Wallid Deb, et al.
Journal of Crohn'S & Colitis|September 8, 2025
Blood proteomic signatures associated with disease activity in inflammatory bowel diseasesMaëva Veyssière, Nassim Hammoudi, Lionel Le Bourhis, et al.
Frontiers in Immunology|September 13, 2023
The risk of COVID-19 in IBD patients is increased by urban living and is not influenced by disease activity or intravenous biologicsMargaux Lelong, Régis Josien, Marianne Coste-Burel, et al.
Aging Clinical and Experimental Research|December 24, 2024
Clinical outcomes from robotic transabdominal preperitoneal inguinal hernia repair in patients under and over 70 years old: a single institution retrospective cohort study with a comprehensive systematic review on behalf of TROGSS - The Robotic Global Surgical SocietyYeisson Rivero-Moreno, Aman Goyal, Samantha Redden-Chirinos, et al.
Brain : a Journal of Neurology|June 8, 2018
De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel geneJean Chemin, Karine Siquier-Pernet, Michaël Nicouleau, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2023
Deficiency of the minor spliceosome component U4atac snRNA secondarily results in ciliary defects in human and zebrafishDeepak Khatri, Audrey Putoux, Audric Cologne, et al.
Pageof 15

Showing results (121-130 of 147) with videos related to

Sort By:
Pageof 15
Human Genetics|February 7, 2025
Unilateral, bilateral symmetric or asymmetric isolated hearing loss in patients with heterozygous KITLG variantsMargaux Serey-Gaut, Ralyath Balogoun, Laurence Jonard, et al.
Cell Host & Microbe|September 18, 2021
Genomic and functional characterization of a mucosal symbiont involved in early-stage colorectal cancerMelissa C Kordahi, Ian B Stanaway, Marion Avril, et al.
Genome Research|April 4, 2008
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repairMarijke Bauters, Hilde Van Esch, Michael J Friez, et al.
Gastroenterology|February 26, 2026
Uncovering the dynamics of mucosa-associated microbiota in post-operative recurrence of Crohn's diseaseLéonard Dubois, Alexandre Chaussard, Philippe Seksik, et al.
Journal of Medical Genetics|September 17, 2025
Heterozygous alterations of <i>GTF2I</i> at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorderJeanne Jury, Thomas Besnard, Wallid Deb, et al.
Journal of Crohn'S & Colitis|September 8, 2025
Blood proteomic signatures associated with disease activity in inflammatory bowel diseasesMaëva Veyssière, Nassim Hammoudi, Lionel Le Bourhis, et al.
Frontiers in Immunology|September 13, 2023
The risk of COVID-19 in IBD patients is increased by urban living and is not influenced by disease activity or intravenous biologicsMargaux Lelong, Régis Josien, Marianne Coste-Burel, et al.
Aging Clinical and Experimental Research|December 24, 2024
Clinical outcomes from robotic transabdominal preperitoneal inguinal hernia repair in patients under and over 70 years old: a single institution retrospective cohort study with a comprehensive systematic review on behalf of TROGSS - The Robotic Global Surgical SocietyYeisson Rivero-Moreno, Aman Goyal, Samantha Redden-Chirinos, et al.
Brain : a Journal of Neurology|June 8, 2018
De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel geneJean Chemin, Karine Siquier-Pernet, Michaël Nicouleau, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2023
Deficiency of the minor spliceosome component U4atac snRNA secondarily results in ciliary defects in human and zebrafishDeepak Khatri, Audrey Putoux, Audric Cologne, et al.
Pageof 15