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T Arold

Showing results (161-170 of 187) with videos related to

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Nucleic Acids Research|January 1, 2019
H-NS uses an autoinhibitory conformational switch for environment-controlled gene silencingUmar F Shahul Hameed, Chenyi Liao, Anand K Radhakrishnan, et al.
Frontiers in Molecular Neuroscience|July 5, 2022
<i>SPTBN5</i>, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and SeizuresAmjad Khan, Lucia Pia Bruno, Fadhel Alomar, et al.
Molecular Genetics and Metabolism|March 12, 2026
TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab familiesMalak Alghamdi, Ahmad Alahmad, Malak Alaboudi, et al.
Cells|October 14, 2022
A Novel Homozygous Founder Variant of <i>RTN4IP1</i> in Two Consanguineous Saudi FamiliesMazhor Aldosary, Maysoon Alsagob, Hanan AlQudairy, et al.
Cell Host & Microbe|July 11, 2014
Genome-wide functional analysis of Plasmodium protein phosphatases reveals key regulators of parasite development and differentiationDavid S Guttery, Benoit Poulin, Abhinay Ramaprasad, et al.
The ISME Journal|June 10, 2025
Widespread distribution of bacteria containing PETases with a functional motif across global oceansIntikhab Alam, Ramona Marasco, Afaque A Momin, et al.
The Journal of Clinical Investigation|November 17, 2015
PRMT1-mediated methylation of the EGF receptor regulates signaling and cetuximab responseHsin-Wei Liao, Jung-Mao Hsu, Weiya Xia, et al.
Brain : a Journal of Neurology|June 6, 2018
Biallelic UFM1 and UFC1 mutations expand the essential role of ufmylation in brain developmentMichael S Nahorski, Sateesh Maddirevula, Ryosuke Ishimura, et al.
Ebiomedicine|May 10, 2025
SLK is mutated in individuals with a neurodevelopmental disorderLama Alabdi, Norah Altuwaijri, Jun-Yi Zhu, et al.
Nature Communications|December 5, 2015
MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumoursElizabeth J Perlman, Samantha Gadd, Stefan T Arold, et al.
Pageof 19

Showing results (161-170 of 187) with videos related to

Sort By:
Pageof 19
Nucleic Acids Research|January 1, 2019
H-NS uses an autoinhibitory conformational switch for environment-controlled gene silencingUmar F Shahul Hameed, Chenyi Liao, Anand K Radhakrishnan, et al.
Frontiers in Molecular Neuroscience|July 5, 2022
<i>SPTBN5</i>, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and SeizuresAmjad Khan, Lucia Pia Bruno, Fadhel Alomar, et al.
Molecular Genetics and Metabolism|March 12, 2026
TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab familiesMalak Alghamdi, Ahmad Alahmad, Malak Alaboudi, et al.
Cells|October 14, 2022
A Novel Homozygous Founder Variant of <i>RTN4IP1</i> in Two Consanguineous Saudi FamiliesMazhor Aldosary, Maysoon Alsagob, Hanan AlQudairy, et al.
Cell Host & Microbe|July 11, 2014
Genome-wide functional analysis of Plasmodium protein phosphatases reveals key regulators of parasite development and differentiationDavid S Guttery, Benoit Poulin, Abhinay Ramaprasad, et al.
The ISME Journal|June 10, 2025
Widespread distribution of bacteria containing PETases with a functional motif across global oceansIntikhab Alam, Ramona Marasco, Afaque A Momin, et al.
The Journal of Clinical Investigation|November 17, 2015
PRMT1-mediated methylation of the EGF receptor regulates signaling and cetuximab responseHsin-Wei Liao, Jung-Mao Hsu, Weiya Xia, et al.
Brain : a Journal of Neurology|June 6, 2018
Biallelic UFM1 and UFC1 mutations expand the essential role of ufmylation in brain developmentMichael S Nahorski, Sateesh Maddirevula, Ryosuke Ishimura, et al.
Ebiomedicine|May 10, 2025
SLK is mutated in individuals with a neurodevelopmental disorderLama Alabdi, Norah Altuwaijri, Jun-Yi Zhu, et al.
Nature Communications|December 5, 2015
MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumoursElizabeth J Perlman, Samantha Gadd, Stefan T Arold, et al.
Pageof 19