Homo sapiens NFKB activating protein (NKAP), RefSeqGene on chromosome - Nucleotide

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From phenotype to mechanism: Prenatal spectrum of NKAP mutation-related disorder and its pathogenesis inducing congenital heart disease. [J Cell Mol Med. 2024]
From phenotype to mechanism: Prenatal spectrum of NKAP mutation-related disorder and its pathogenesis inducing congenital heart disease.
Xu X, Gao C, Ye F, Peng A, Xu J, Jin K, Zhang J, Ye Y, Yang Y, Zhang X, et al. J Cell Mol Med. 2024 Apr; 28(8):e18305.
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.
TXLNA enhances TBK1 phosphorylation by suppressing PPM1B recruitment. [Biochim Biophys Acta Mol Cell ...]
TXLNA enhances TBK1 phosphorylation by suppressing PPM1B recruitment.
Tian X, Zhang Z, Ding M. Biochim Biophys Acta Mol Cell Res. 2023 Oct; 1870(7):119550. Epub 2023 Jul 26.

Protein
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Homo sapiens NFKB activating protein (NKAP), RefSeqGene on chromosome X
Homo sapiens NFKB activating protein (NKAP), RefSeqGene on chromosome X
gi|296278249|ref|NG_021260.1|

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Nucleotide