Wei YH - Search Results

1

Peptide-mediated delivery of donor mitochondria improves mitochondrial function and cell viability in human cybrid cells with the MELAS A3243G mutation.

Chang JC, Hoel F, Liu KH, Wei YH, Cheng FC, Kuo SJ, Tronstad KJ, Liu CS. Chang JC, et al. Among authors: wei yh. Sci Rep. 2017 Sep 6;7(1):10710. doi: 10.1038/s41598-017-10870-5. Sci Rep. 2017. PMID: 28878349 Free PMC article.

2

Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS): report of a sporadic case and review of the literature.

Lee ML, Chaou WT, Yang AD, Jong YJ, Tsai JL, Pang CY, Wei YH. Lee ML, et al. Among authors: wei yh. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1994 Mar-Apr;35(2):148-56. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1994. PMID: 8184691

3

MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family.

Huang CC, Chen RS, Chen CM, Wang HS, Lee CC, Pang CY, Hsu HS, Lee HC, Wei YH. Huang CC, et al. Among authors: wei yh. J Neurol Neurosurg Psychiatry. 1994 May;57(5):586-9. doi: 10.1136/jnnp.57.5.586. J Neurol Neurosurg Psychiatry. 1994. PMID: 8201329 Free PMC article.

4

Type IV hyperlipoproteinemia and moderate instability of CAG triplet expansion in the androgen-receptor gene. Lipid, sex hormone and molecular study in a Chinese family with Kennedy-Alter-Sung disease.

Liu CS, Chang YC, Chen DF, Huang CC, Pang CY, Lee HC, Cheng CC, Horng CJ, Wei YH. Liu CS, et al. Among authors: wei yh. Acta Neurol Scand. 1995 Nov;92(5):398-404. doi: 10.1111/j.1600-0404.1995.tb00154.x. Acta Neurol Scand. 1995. PMID: 8610494

5

MELAS syndrome associated with a tandem duplication in the D-loop of mitochondrial DNA.

Li JY, Kong KW, Chang MH, Cheung SC, Lee HC, Pang CY, Wei YH. Li JY, et al. Among authors: wei yh. Acta Neurol Scand. 1996 Jun;93(6):450-5. doi: 10.1111/j.1600-0404.1996.tb00025.x. Acta Neurol Scand. 1996. PMID: 8836308

6

Phenytoin-mediated oxidative stress in serum of female epileptics: a possible pathogenesis in the fetal hydantoin syndrome.

Liu CS, Wu HM, Kao SH, Wei YH. Liu CS, et al. Among authors: wei yh. Hum Exp Toxicol. 1997 Mar;16(3):177-81. doi: 10.1177/096032719701600308. Hum Exp Toxicol. 1997. PMID: 9088972

7

Ageing-associated large-scale deletions of mitochondrial DNA in human hair follicles.

Kao SH, Liu CS, Wang SY, Wei YH. Kao SH, et al. Among authors: wei yh. Biochem Mol Biol Int. 1997 Jun;42(2):285-98. doi: 10.1080/15216549700202681. Biochem Mol Biol Int. 1997. PMID: 9238527

8

Smoking-associated mitochondrial DNA mutations in human hair follicles.

Liu CS, Kao SH, Wei YH. Liu CS, et al. Among authors: wei yh. Environ Mol Mutagen. 1997;30(1):47-55. doi: 10.1002/(sici)1098-2280(1997)30:1<47::aid-em7>3.0.co;2-9. Environ Mol Mutagen. 1997. PMID: 9258329

9

Prevalence of apolipoprotein E genotypes in ischaemic cerebrovascular disease in end-stage renal disease patients.

Lim PS, Liu CS, Hong CJ, Wei YH. Lim PS, et al. Among authors: wei yh. Nephrol Dial Transplant. 1997 Sep;12(9):1916-20. doi: 10.1093/ndt/12.9.1916. Nephrol Dial Transplant. 1997. PMID: 9306343

10

Mutation and oxidative damage of mitochondrial DNA and defective turnover of mitochondria in human aging.

Lee HC, Wei YH. Lee HC, et al. Among authors: wei yh. J Formos Med Assoc. 1997 Oct;96(10):770-8. J Formos Med Assoc. 1997. PMID: 9343975 Review.

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