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Thomas Arnesen

Showing results (101-110 of 116) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 28, 2018
Structural determinants and cellular environment define processed actin as the sole substrate of the N-terminal acetyltransferase NAA80Marianne Goris, Robert S Magin, Håvard Foyn, et al.
Journal of Inherited Metabolic Disease|September 3, 2020
Functional evaluation of 16 SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss-of-function phenotypes in vitroKelly Velasco, Johanna L St-Louis, Henrikke N Hovland, et al.
Nature Communications|July 18, 2015
Downregulation of N-terminal acetylation triggers ABA-mediated drought responses in ArabidopsisEric Linster, Iwona Stephan, Willy V Bienvenut, et al.
JCI Insight|June 10, 2024
Molecular mechanism of HNF-1A-mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetesLaura Kind, Janne Molnes, Erling Tjora, et al.
Cell Reports|March 4, 2015
An organellar nα-acetyltransferase, naa60, acetylates cytosolic N termini of transmembrane proteins and maintains Golgi integrityHenriette Aksnes, Petra Van Damme, Marianne Goris, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 2012
N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatBPetra Van Damme, Marta Lasa, Bogdan Polevoda, et al.
Human Molecular Genetics|December 10, 2014
Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defectsLine M Myklebust, Petra Van Damme, Svein I Støve, et al.
European Journal of Human Genetics : EJHG|May 12, 2018
A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathySvein Isungset Støve, Marina Blenski, Asbjørg Stray-Pedersen, et al.
Clinical Genetics|May 16, 2023
Novel biallelic variants expand the phenotype of NAA20-related syndromeGianluca D'Onofrio, Claudia Cuccurullo, Silje Kathrine Larsen, et al.
Nature Communications|October 27, 2023
N-terminal acetylation shields proteins from degradation and promotes age-dependent motility and longevitySylvia Varland, Rui Duarte Silva, Ine Kjosås, et al.
Pageof 12

Showing results (101-110 of 116) with videos related to

Sort By:
Pageof 12
Proceedings of the National Academy of Sciences of the United States of America|March 28, 2018
Structural determinants and cellular environment define processed actin as the sole substrate of the N-terminal acetyltransferase NAA80Marianne Goris, Robert S Magin, Håvard Foyn, et al.
Journal of Inherited Metabolic Disease|September 3, 2020
Functional evaluation of 16 SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss-of-function phenotypes in vitroKelly Velasco, Johanna L St-Louis, Henrikke N Hovland, et al.
Nature Communications|July 18, 2015
Downregulation of N-terminal acetylation triggers ABA-mediated drought responses in ArabidopsisEric Linster, Iwona Stephan, Willy V Bienvenut, et al.
JCI Insight|June 10, 2024
Molecular mechanism of HNF-1A-mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetesLaura Kind, Janne Molnes, Erling Tjora, et al.
Cell Reports|March 4, 2015
An organellar nα-acetyltransferase, naa60, acetylates cytosolic N termini of transmembrane proteins and maintains Golgi integrityHenriette Aksnes, Petra Van Damme, Marianne Goris, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 2012
N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatBPetra Van Damme, Marta Lasa, Bogdan Polevoda, et al.
Human Molecular Genetics|December 10, 2014
Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defectsLine M Myklebust, Petra Van Damme, Svein I Støve, et al.
European Journal of Human Genetics : EJHG|May 12, 2018
A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathySvein Isungset Støve, Marina Blenski, Asbjørg Stray-Pedersen, et al.
Clinical Genetics|May 16, 2023
Novel biallelic variants expand the phenotype of NAA20-related syndromeGianluca D'Onofrio, Claudia Cuccurullo, Silje Kathrine Larsen, et al.
Nature Communications|October 27, 2023
N-terminal acetylation shields proteins from degradation and promotes age-dependent motility and longevitySylvia Varland, Rui Duarte Silva, Ine Kjosås, et al.
Pageof 12