Human NCKX6 (pcDNA3.1+) Citations (2)

Originally described in: Molecular cloning of a sixth member of the K+-dependent Na+/Ca2+ exchanger gene family, NCKX6.
Cai X, Lytton J J Biol Chem. 2004 Feb 13;279(7):5867-76. Epub 2003 Nov 18. PubMed Journal

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Articles Citing Human NCKX6 (pcDNA3.1+)

Articles
Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. Stavsky A, Stoler O, Kostic M, Katoshevsky T, Assali EA, Savic I, Amitai Y, Prokisch H, Leiz S, Daumer-Haas C, Fleidervish I, Perocchi F, Gitler D, Sekler I. Commun Biol. 2021 Jun 2;4(1):666. doi: 10.1038/s42003-021-02114-0. PubMed
Partial loss of MCU mitigates pathology in vivo across a diverse range of neurodegenerative disease models. Twyning MJ, Tufi R, Gleeson TP, Kolodziej KM, Campesan S, Terriente-Felix A, Collins L, De Lazzari F, Giorgini F, Whitworth AJ. Cell Rep. 2024 Feb 27;43(2):113681. doi: 10.1016/j.celrep.2024.113681. Epub 2024 Jan 18. PubMed

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