Liu H - Search Results

1

A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.

Wang M, Peng Y, Zheng J, Zheng B, Jin X, Liu H, Wang Y, Tang X, Huang T, Jiang P, Guan MX. Wang M, et al. Among authors: liu h. Nucleic Acids Res. 2016 Dec 15;44(22):10974-10985. doi: 10.1093/nar/gkw726. Epub 2016 Aug 17. Nucleic Acids Res. 2016. PMID: 27536005 Free PMC article.

2

Human Bex2 interacts with LMO2 and regulates the transcriptional activity of a novel DNA-binding complex.

Han C, Liu H, Liu J, Yin K, Xie Y, Shen X, Wang Y, Yuan J, Qiang B, Liu YJ, Peng X. Han C, et al. Among authors: liu j, liu yj, liu h. Nucleic Acids Res. 2005 Nov 24;33(20):6555-65. doi: 10.1093/nar/gki964. Print 2005. Nucleic Acids Res. 2005. PMID: 16314316 Free PMC article.

3

Loss of MED1 triggers mitochondrial biogenesis in C2C12 cells.

Yu J, Xiao Y, Liu J, Ji Y, Liu H, Xu J, Jin X, Liu L, Guan MX, Jiang P. Yu J, et al. Among authors: liu j, liu h, liu l. Mitochondrion. 2014 Jan;14(1):18-25. doi: 10.1016/j.mito.2013.12.004. Epub 2013 Dec 22. Mitochondrion. 2014. PMID: 24368311

4

Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene.

Liu H, Li R, Li W, Wang M, Ji J, Zheng J, Mao Z, Mo JQ, Jiang P, Lu J, Guan MX. Liu H, et al. Mitochondrion. 2015 Mar;21:49-57. doi: 10.1016/j.mito.2015.01.004. Epub 2015 Jan 20. Mitochondrion. 2015. PMID: 25615420

5

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.

Jiang P, Jin X, Peng Y, Wang M, Liu H, Liu X, Zhang Z, Ji Y, Zhang J, Liang M, Zhao F, Sun YH, Zhang M, Zhou X, Chen Y, Mo JQ, Huang T, Qu J, Guan MX. Jiang P, et al. Among authors: liu h, liu x. Hum Mol Genet. 2016 Feb 1;25(3):584-96. doi: 10.1093/hmg/ddv498. Epub 2015 Dec 8. Hum Mol Genet. 2016. PMID: 26647310

6

A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function.

Jiang P, Wang M, Xue L, Xiao Y, Yu J, Wang H, Yao J, Liu H, Peng Y, Liu H, Li H, Chen Y, Guan MX. Jiang P, et al. Among authors: liu h. Mol Cell Biol. 2016 Jun 29;36(14):1920-30. doi: 10.1128/MCB.00199-16. Print 2016 Jul 15. Mol Cell Biol. 2016. PMID: 27161322 Free PMC article.

7

A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.

Wang M, Liu H, Zheng J, Chen B, Zhou M, Fan W, Wang H, Liang X, Zhou X, Eriani G, Jiang P, Guan MX. Wang M, et al. Among authors: liu h. J Biol Chem. 2016 Sep 30;291(40):21029-21041. doi: 10.1074/jbc.M116.739482. Epub 2016 Aug 12. J Biol Chem. 2016. PMID: 27519417 Free PMC article.

8

Association analysis of mitochondrial genome polymorphisms with backfat thickness in pigs.

Liu H, Zhang X, Hu Y, Zhao X. Liu H, et al. Anim Biotechnol. 2023 Oct 27;35(1):2272172. doi: 10.1080/10495398.2023.2272172. Epub 2023 Nov 15. Anim Biotechnol. 2023. PMID: 37966129 Free article.

9

Mitochondrial DNA enrichment reduced NUMT contamination in porcine NGS analyses.

Wang D, Xiang H, Ning C, Liu H, Liu JF, Zhao X. Wang D, et al. Among authors: liu h, liu jf. Brief Bioinform. 2020 Jul 15;21(4):1368-1377. doi: 10.1093/bib/bbz060. Brief Bioinform. 2020. PMID: 31204429

10

Fecal microbiota transplantation provides insights into the consequences of transcriptome profiles and cell energy in response to circadian misalignment of chickens.

Chen S, Liu H, Yan C, Li Y, Xiao J, Zhao X. Chen S, et al. Among authors: liu h. Poult Sci. 2024 Sep;103(9):103926. doi: 10.1016/j.psj.2024.103926. Epub 2024 Jun 6. Poult Sci. 2024. PMID: 38964253 Free PMC article.

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