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hu meng wen[Author]
(18 results)?
Breast cancer-associated mitochondrial DNA haplogroup promotes neoplastic growth via ROS-mediated AKT activation.
Int J Cancer. 2018 May 1;142(9):1786-1796. doi: 10.1002/ijc.31207. Epub 2017 Dec 20.
Int J Cancer. 2018.
PMID: 29226320
Free article.
Mutations in FASTKD2 are associated with mitochondrial disease with multi-OXPHOS deficiency.
Wei X, Du M, Li D, Wen S, Xie J, Li Y, Chen A, Zhang K, Xu P, Jia M, Wen C, Zhou H, Lyu J, Yang Y, Fang H.
Wei X, et al. Among authors: wen s.
Hum Mutat. 2020 May;41(5):961-972. doi: 10.1002/humu.23985. Epub 2020 Jan 30.
Hum Mutat. 2020.
PMID: 31944455
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Bilateral striatal necrosis due to homoplasmic mitochondrial 3697G>A mutation presents with incomplete penetrance and sex bias.
Zhong S, Wen S, Qiu Y, Yu Y, Xin L, He Y, Gao X, Fang H, Hong D, Zhang J.
Zhong S, et al. Among authors: wen s.
Mol Genet Genomic Med. 2019 Mar;7(3):e541. doi: 10.1002/mgg3.541. Epub 2019 Jan 8.
Mol Genet Genomic Med. 2019.
PMID: 30623604
Free PMC article.
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A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
Lou X, Shi H, Wen S, Li Y, Wei X, Xie J, Ma L, Yang Y, Fang H, Lyu J.
Lou X, et al. Among authors: wen s.
J Hum Genet. 2018 Dec;63(12):1269-1272. doi: 10.1038/s10038-018-0505-0. Epub 2018 Aug 23.
J Hum Genet. 2018.
PMID: 30140060
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Comparison of paired cerebrospinal fluid and serum cell-free mitochondrial and nuclear DNA with copy number and fragment length.
Chen A, Li J, Wang L, Huang Q, Zhu J, Wen S, Lyu J, Wu W.
Chen A, et al. Among authors: wen s.
J Clin Lab Anal. 2020 Jun;34(6):e23238. doi: 10.1002/jcla.23238. Epub 2020 Feb 13.
J Clin Lab Anal. 2020.
PMID: 32052892
Free PMC article.
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SURF1 mutations in Chinese patients with Leigh syndrome: Novel mutations, mutation spectrum, and the functional consequences.
Li Y, Wen S, Li D, Xie J, Wei X, Li X, Liu Y, Fang H, Yang Y, Lyu J.
Li Y, et al. Among authors: wen s.
Gene. 2018 Oct 20;674:15-24. doi: 10.1016/j.gene.2018.06.058. Epub 2018 Jun 19.
Gene. 2018.
PMID: 29933018
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Correction: A novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
Lou X, Shi H, Wen S, Li Y, Wei X, Xie J, Ma L, Yang Y, Fang H, Lyu J.
Lou X, et al. Among authors: wen s.
J Hum Genet. 2018 Dec;63(12):1283-1284. doi: 10.1038/s10038-018-0517-9.
J Hum Genet. 2018.
PMID: 30266949
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