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Year Number of Results
2009 1
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2013 1
2014 2
2015 3
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2024 4

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Page 1
The regulation and function of the NUAK family.
Sun X, Gao L, Chien HY, Li WC, Zhao J. Sun X, et al. Among authors: chien hy. J Mol Endocrinol. 2013 Sep 10;51(2):R15-22. doi: 10.1530/JME-13-0063. Print 2013 Oct. J Mol Endocrinol. 2013. PMID: 23873311 Review.
UQCRC1 engages cytochrome c for neuronal apoptotic cell death.
Hung YC, Huang KL, Chen PL, Li JL, Lu SH, Chang JC, Lin HY, Lo WC, Huang SY, Lee TT, Lin TY, Imai Y, Hattori N, Liu CS, Tsai SY, Chen CH, Lin CH, Chan CC. Hung YC, et al. Cell Rep. 2021 Sep 21;36(12):109729. doi: 10.1016/j.celrep.2021.109729. Cell Rep. 2021. PMID: 34551295 Free article.
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
Lin CH, Tsai PI, Lin HY, Hattori N, Funayama M, Jeon B, Sato K, Abe K, Mukai Y, Takahashi Y, Li Y, Nishioka K, Yoshino H, Daida K, Chen ML, Cheng J, Huang CY, Tzeng SR, Wu YS, Lai HJ, Tsai HH, Yen RF, Lee NC, Lo WC, Hung YC, Chan CC, Ke YC, Chao CC, Hsieh ST, Farrer M, Wu RM. Lin CH, et al. Among authors: hung yc. Brain. 2020 Dec 5;143(11):3352-3373. doi: 10.1093/brain/awaa279. Brain. 2020. PMID: 33141179 Free PMC article.
A missense mutation in human INSC causes peripheral neuropathy.
Yeh JY, Chao HC, Hong CL, Hung YC, Tzou FY, Hsiao CT, Li JL, Chen WJ, Chou CT, Tsai YS, Liao YC, Lin YC, Lin S, Huang SY, Kennerson M, Lee YC, Chan CC. Yeh JY, et al. Among authors: hung yc. EMBO Mol Med. 2024 Apr 8. doi: 10.1038/s44321-024-00062-w. Online ahead of print. EMBO Mol Med. 2024. PMID: 38589651 Free article.
25 results