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Showing results (41-50 of 196) with videos related to

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Neurogenetics|May 25, 2024
Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disabilitySaima, Amjad Khan, Sajid Ali, et al.
Journal of Molecular Biology|November 11, 2003
Crystal structure of the N-terminal dimerisation domain of VicH, the H-NS-like protein of Vibrio choleraeRachel Cerdan, Vanessa Bloch, Yinshan Yang, et al.
Neurogenetics|April 12, 2019
Truncating biallelic variant in DNAJA1, encoding the co-chaperone Hsp40, is associated with intellectual disability and seizuresSaud Alsahli, Ahmed Alfares, Francisco J Guzmán-Vega, et al.
Genome Biology|May 1, 2019
CRISPR directed evolution of the spliceosome for resistance to splicing inhibitorsHaroon Butt, Ayman Eid, Afaque A Momin, et al.
Ophthalmic Genetics|August 2, 2018
Familial non-syndromic macular pseudocoloboma secondary to homozygous CLDN19 mutationArif O Khan, Nisha Patel, Nicola G Ghazi, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 14, 2007
Structure of PlcR: Insights into virulence regulation and evolution of quorum sensing in Gram-positive bacteriaNathalie Declerck, Laurent Bouillaut, Denis Chaix, et al.
Human Genome Variation|February 22, 2023
SHQ1-associated neurodevelopmental disorder: Report of the first homozygous variant in unrelated patients and review of the literatureAljouhra AlHargan, Mohammed A AlMuhaizea, Rawan Almass, et al.
Nature Communications|November 21, 2025
Mechanism of cooperative strigolactone perception by the MAX2 ubiquitin ligase-receptor-substrate complexAlexandra I Vancea, Brandon Huntington, Wieland Steinchen, et al.
Human Genomics|August 12, 2021
Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data miningMohamed Abouelhoda, Dania Mohty, Islam Alayary, et al.
International Dental Journal|June 24, 2025
A Novel KDF1 Variant is Associated With Multiple Natal Teeth, Tooth Agenesis, and Root MaldevelopmentJohn M Graham, Pedro A Sanchez-Lara, Atsushi Ohazama, et al.
Pageof 20

Showing results (41-50 of 196) with videos related to

Sort By:
Pageof 20
Neurogenetics|May 25, 2024
Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disabilitySaima, Amjad Khan, Sajid Ali, et al.
Journal of Molecular Biology|November 11, 2003
Crystal structure of the N-terminal dimerisation domain of VicH, the H-NS-like protein of Vibrio choleraeRachel Cerdan, Vanessa Bloch, Yinshan Yang, et al.
Neurogenetics|April 12, 2019
Truncating biallelic variant in DNAJA1, encoding the co-chaperone Hsp40, is associated with intellectual disability and seizuresSaud Alsahli, Ahmed Alfares, Francisco J Guzmán-Vega, et al.
Genome Biology|May 1, 2019
CRISPR directed evolution of the spliceosome for resistance to splicing inhibitorsHaroon Butt, Ayman Eid, Afaque A Momin, et al.
Ophthalmic Genetics|August 2, 2018
Familial non-syndromic macular pseudocoloboma secondary to homozygous CLDN19 mutationArif O Khan, Nisha Patel, Nicola G Ghazi, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 14, 2007
Structure of PlcR: Insights into virulence regulation and evolution of quorum sensing in Gram-positive bacteriaNathalie Declerck, Laurent Bouillaut, Denis Chaix, et al.
Human Genome Variation|February 22, 2023
SHQ1-associated neurodevelopmental disorder: Report of the first homozygous variant in unrelated patients and review of the literatureAljouhra AlHargan, Mohammed A AlMuhaizea, Rawan Almass, et al.
Nature Communications|November 21, 2025
Mechanism of cooperative strigolactone perception by the MAX2 ubiquitin ligase-receptor-substrate complexAlexandra I Vancea, Brandon Huntington, Wieland Steinchen, et al.
Human Genomics|August 12, 2021
Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data miningMohamed Abouelhoda, Dania Mohty, Islam Alayary, et al.
International Dental Journal|June 24, 2025
A Novel KDF1 Variant is Associated With Multiple Natal Teeth, Tooth Agenesis, and Root MaldevelopmentJohn M Graham, Pedro A Sanchez-Lara, Atsushi Ohazama, et al.
Pageof 20