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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 NAA80
Marianne 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 vitro
Kelly 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 Arabidopsis
Eric 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 diabetes
Laura 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 integrity
Henriette 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 NatB
Petra 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 defects
Line 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 cardiomyopathy
Svein Isungset Støve, Marina Blenski, Asbjørg Stray-Pedersen, et al.
Clinical Genetics
|
May 16, 2023
Novel biallelic variants expand the phenotype of NAA20-related syndrome
Gianluca 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 longevity
Sylvia Varland, Rui Duarte Silva, Ine Kjosås, et al.
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Showing results (101-110 of 116) with videos related to
Sort By:
Page
of 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 NAA80
Marianne 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 vitro
Kelly 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 Arabidopsis
Eric 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 diabetes
Laura 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 integrity
Henriette 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 NatB
Petra 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 defects
Line 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 cardiomyopathy
Svein Isungset Støve, Marina Blenski, Asbjørg Stray-Pedersen, et al.
Clinical Genetics
|
May 16, 2023
Novel biallelic variants expand the phenotype of NAA20-related syndrome
Gianluca 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 longevity
Sylvia Varland, Rui Duarte Silva, Ine Kjosås, et al.
Page
of 12