Vitenskapelig artikkel

• Aksnes, Henriette; McTiernan, Nina ; Arnesen, Thomas (2023). NATs at a glance. (ekstern lenke)
• McTiernan, Nina; Tranebjærg, Lisbeth; Bjørheim, Anna Steensen et al. (2022). Biochemical analysis of novel NAA10 variants suggests distinct pathogenic mechanisms involving impaired protein N-terminal acetylation. (ekstern lenke)
• Kweon, Hyae Yon; Lee, Mi-Ni; Dörfel, Max J et al. (2021). Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway. (ekstern lenke)
• Ree, Rasmus Moen; Krogstad, Karoline; Tiernan, Nina Mc et al. (2021). Hydroxylation of the acetyltransferase NAA10 Trp38 is not an enzyme-switch in human cells. (ekstern lenke)
• Bader, Ingrid; Mc Tiernan, Nina; Darbakk, Christine et al. (2020). Severe syndromic ID and skewed X-inactivation in a girl with NAA10 dysfunction and a novel heterozygous de novo NAA10 p.(His16Pro) variant - A case report. (ekstern lenke)
• Mc Tiernan, Nina; Darbakk, Christine; Ree, Rasmus et al. (2020). Naa10 p.(d10g) and naa10 p.(l11r) variants hamper formation of the nata n-terminal acetyltransferase complex. (ekstern lenke)
• Mc Tiernan, Nina; Gill, Harinder; Prada, Carlos E. et al. (2020). NAA10 p.(N101K) disrupts N-terminal acetyltransferase complex NatA and is associated with developmental delay and hemihypertrophy. (ekstern lenke)
• Deng, Sunbin; Mc Tiernan, Nina; Wei, Xuepeng et al. (2020). Molecular basis for N-terminal acetylation by human NatE and its modulation by HYPK. (ekstern lenke)
• Støve, Svein Isungset; Blenski, Marina; Stray-Pedersen, Asbjørg et al. (2018). A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy. (ekstern lenke)
• Mc Tiernan, Nina; Støve, Svein Isungset; Aukrust, Ingvild et al. (2018). NAA10 dysfunction with normal NatA-complex activity in a girl with non-syndromic ID and a de novo NAA10 p.(V111G) variant - a case report. (ekstern lenke)

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