Homo sapiens NADH:ubiquinone oxidoreductase complex assembly factor 2 - Nucleotide

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A compound heterozygous mutation of ERCC8 is responsible for a family with Cockayne syndrome. [Mol Biol Rep. 2024]
A compound heterozygous mutation of ERCC8 is responsible for a family with Cockayne syndrome.
Liu MW, Hu CF, Jin JY, Xiang R, Fan LL, Li YL, Zhu L. Mol Biol Rep. 2024 Feb 27; 51(1):371. Epub 2024 Feb 27.
Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortality. [Mitochondrion. 2024]
Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortality.
Sabharwal A, Gupta V, Kv S, Kumar Manokaran R, Verma A, Mishra A, Bhoyar RC, Jain A, Sivadas A, Rawat S, et al. Mitochondrion. 2024 Mar; 75:101844. Epub 2024 Jan 17.
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. [Mol Cell. 2024]
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies.
Chrustowicz J, Sherpa D, Li J, Langlois CR, Papadopoulou EC, Vu DT, Hehl LA, Karayel Ö, Beier V, von Gronau S, et al. Mol Cell. 2024 Jan 18; 84(2):293-308.e14. Epub 2023 Dec 18.

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Nucleotide