Henriette Aksnes

Forsker
ved Institutt for biomedisin ved Universitetet i Bergen

Resultater Resultater

Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications.

Chelban, Viorica; Aksnes, Henriette; Maroofian, Reza; LaMonica, Lauren C.; Seabra, Luis; Siggervåg, Anette; Devic, Perrine; Shamseldin, Hanan E.; Vandrovcova, Jana; Murphy, David mfl.. 2024, Nature Communications. HBKU, HAUKELAND, FREIBURG, UA, OTT, UoO, EGYPT, UNISTRA, DÜ, TYSKLAND, YU, SAUDIARAB, STORBRITAN, GEI, UMG, FRANKRIKE, UIB, TUOE, TYRKIA, UOTTAWA, UCSD, DEÜ, KASAKHSTAN, GNC, UNIVROUEN, UCL, UdMVitenskapelig artikkel

Loss of N-terminal acetyltransferase A activity induces thermally unstable ribosomal proteins and increases their turnover in Saccharomyces cerevisiae.

Guzman, Ulises H.; Aksnes, Henriette; Ree, Rasmus; Krogh, Nicolai; Jakobsson, Magnus; Jensen, Lars J.; Arnesen, Thomas; Olsen, Jesper V.. 2023, Nature Communications. HAUKELAND, Lu, KU, UIBVitenskapelig artikkel

Henriette Aksnes

Resultater Resultater

Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications.

Loss of N-terminal acetyltransferase A activity induces thermally unstable ribosomal proteins and increases their turnover in Saccharomyces cerevisiae.

NATs at a glance.

NAA60 in neurodegenerative disease.

Investigating the biological role of human NAT14 (probable N-acetyltransferase 14).