Academic literature review
Academic article
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Heathcote, Karen C.; Keeley, Thomas P.; Myllykoski, Matti Aukusti
et al. (2024). N-terminal cysteine acetylation and oxidation patterns may define protein stability. (external link)
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Aksnes, Henriette; McTiernan, Nina ; Arnesen, Thomas
(2023). NATs at a glance. (external link)
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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. (external link)
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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. (external link)
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Kweon, Hyae Yon; Lee, Mi-Ni; Dörfel, Max J
et al. (2021). Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway. (external link)
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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. (external link)
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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. (external link)
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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. (external link)
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Deng, Sunbin; Mc Tiernan, Nina; Wei, Xuepeng
et al. (2020). Molecular basis for N-terminal acetylation by human NatE and its modulation by HYPK. (external link)
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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. (external link)
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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. (external link)
See a complete overview of publications in Cristin.
