Meng F - Search Results

1

Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.

Ji Y, Zhang J, Lu Y, Yi Q, Chen M, Xie S, Mao X, Xiao Y, Meng F, Zhang M, Yang R, Guan MX. Ji Y, et al. Among authors: meng f. J Biol Chem. 2020 Sep 18;295(38):13224-13238. doi: 10.1074/jbc.RA120.014603. Epub 2020 Jul 28. J Biol Chem. 2020. PMID: 32723871 Free PMC article.

2

Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation.

Meng F, Cang X, Peng Y, Li R, Zhang Z, Li F, Fan Q, Guan AS, Fischel-Ghosian N, Zhao X, Guan MX. Meng F, et al. J Biol Chem. 2017 Feb 17;292(7):2881-2892. doi: 10.1074/jbc.M116.749374. Epub 2017 Jan 3. J Biol Chem. 2017. PMID: 28049726 Free PMC article.

3

A hypertension-associated mitochondrial DNA mutation introduces an m¹G37 modification into tRNA^Met, altering its structure and function.

Zhou M, Xue L, Chen Y, Li H, He Q, Wang B, Meng F, Wang M, Guan MX. Zhou M, et al. Among authors: meng f. J Biol Chem. 2018 Jan 26;293(4):1425-1438. doi: 10.1074/jbc.RA117.000317. Epub 2017 Dec 8. J Biol Chem. 2018. PMID: 29222331 Free PMC article.

4

Contribution of the tRNA^Ile 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation.

Meng F, He Z, Tang X, Zheng J, Jin X, Zhu Y, Ren X, Zhou M, Wang M, Gong S, Mo JQ, Shu Q, Guan MX. Meng F, et al. J Biol Chem. 2018 Mar 2;293(9):3321-3334. doi: 10.1074/jbc.RA117.000530. Epub 2018 Jan 18. J Biol Chem. 2018. PMID: 29348176 Free PMC article.

5

Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.

Ji Y, Zhang J, Yu J, Wang Y, Lu Y, Liang M, Li Q, Jin X, Wei Y, Meng F, Gao Y, Cang X, Tong Y, Liu X, Zhang M, Jiang P, Zhu T, Mo JQ, Huang T, Jiang P, Guan MX. Ji Y, et al. Among authors: meng f. Hum Mol Genet. 2019 May 1;28(9):1515-1529. doi: 10.1093/hmg/ddy450. Hum Mol Genet. 2019. PMID: 30597069

6

Inhibiting neddylation modification alters mitochondrial morphology and reprograms energy metabolism in cancer cells.

Zhou Q, Li H, Li Y, Tan M, Fan S, Cao C, Meng F, Zhu L, Zhao L, Guan MX, Jin H, Sun Y. Zhou Q, et al. Among authors: meng f. JCI Insight. 2019 Feb 21;4(4):e121582. doi: 10.1172/jci.insight.121582. eCollection 2019 Feb 21. JCI Insight. 2019. PMID: 30668548 Free PMC article.

7

Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNA^His mutation.

Gong S, Wang X, Meng F, Cui L, Yi Q, Zhao Q, Cang X, Cai Z, Mo JQ, Liang Y, Guan MX. Gong S, et al. Among authors: meng f. J Biol Chem. 2020 Jan 24;295(4):940-954. doi: 10.1074/jbc.RA119.010998. Epub 2019 Dec 9. J Biol Chem. 2020. PMID: 31819004 Free PMC article.

8

Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family.

Wang J, Zhao N, Mao X, Meng F, Huang K, Dong G, Ji Y, Fu J. Wang J, et al. Among authors: meng f. Biosci Rep. 2020 Jan 31;40(1):BSR20192153. doi: 10.1042/BSR20192153. Biosci Rep. 2020. PMID: 31868206 Free PMC article.

9

Reply to comments on: "Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family".

Wang J, Zhao N, Mao X, Meng F, Huang K, Dong G, Ji Y, Fu J. Wang J, et al. Among authors: meng f. Biosci Rep. 2020 Feb 28;40(2):BSR20200131. doi: 10.1042/BSR20200131. Biosci Rep. 2020. PMID: 32003422 Free PMC article. No abstract available.

10

Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss.

Zheng J, Bai X, Xiao Y, Ji Y, Meng F, Aishanjiang M, Gao Y, Wang H, Fu Y, Guan MX. Zheng J, et al. Among authors: meng f. Mitochondrion. 2020 May;52:163-172. doi: 10.1016/j.mito.2020.03.005. Epub 2020 Mar 10. Mitochondrion. 2020. PMID: 32169613 Free article.

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