Wang H - Search Results

1

Genetic analysis of the TMEM230 gene in Chinese Han patients with Parkinson's disease.

Shi CH, Li F, Shi MM, Yang ZH, Mao CY, Zhang SY, Wang H, Cheng Y, Yang J, Wu J, Xu YM. Shi CH, et al. Among authors: wang h. Sci Rep. 2017 Apr 26;7(1):1190. doi: 10.1038/s41598-017-01398-9. Sci Rep. 2017. PMID: 28446760 Free PMC article.

2

MC1R variants in Chinese Han patients with sporadic Parkinson's disease.

Shi CH, Wang H, Mao CY, Yang J, Song B, Liu YT, Yang ZH, Luo HY, Zhang SY, Wu J, Xu YM. Shi CH, et al. Among authors: wang h. Neurobiol Aging. 2016 Jun;42:217.e5-6. doi: 10.1016/j.neurobiolaging.2016.02.026. Epub 2016 Mar 3. Neurobiol Aging. 2016. PMID: 27084066

3

DNAJC6 mutations are not common causes of early onset Parkinson's disease in Chinese Han population.

Shi C, Li F, Yang J, Zhang S, Mao C, Wang H, Shi M, Liu Y, Song B, Xu Y. Shi C, et al. Among authors: wang h. Neurosci Lett. 2016 Nov 10;634:60-62. doi: 10.1016/j.neulet.2016.09.044. Epub 2016 Sep 26. Neurosci Lett. 2016. PMID: 27687717

4

SMPD1 variants in Chinese Han patients with sporadic Parkinson's disease.

Mao CY, Yang J, Wang H, Zhang SY, Yang ZH, Luo HY, Li F, Shi M, Liu YT, Zhuang ZP, Du P, Wang YH, Shi CH, Xu YM. Mao CY, et al. Among authors: wang h, wang yh. Parkinsonism Relat Disord. 2017 Jan;34:59-61. doi: 10.1016/j.parkreldis.2016.10.014. Epub 2016 Oct 19. Parkinsonism Relat Disord. 2017. PMID: 27814975

5

Pseudo-dominant inheritance of a novel double GLA mutation associated with Fabry disease mimicking familial episodic pain.

Mao C, Luo H, Yang J, Qin J, Wang H, Song B, Sun S, Zhuang Z, Shi C, Xu Y. Mao C, et al. Among authors: wang h. Am J Med Genet A. 2016 Nov;170(11):3051-3053. doi: 10.1002/ajmg.a.37833. Epub 2016 Aug 17. Am J Med Genet A. 2016. PMID: 27531472 No abstract available.

6

CADASIL mutant NOTCH3(R90C) decreases the viability of HS683 oligodendrocytes via apoptosis.

Tang M, Shi C, Song B, Yang J, Yang T, Mao C, Li Y, Liu X, Zhang S, Wang H, Luo H, Xu Y. Tang M, et al. Among authors: wang h. Mol Biol Rep. 2017 Jul;44(3):273-280. doi: 10.1007/s11033-017-4107-2. Epub 2017 Jun 10. Mol Biol Rep. 2017. PMID: 28601945

7

TAP1 I333V gene polymorphism and type 1 diabetes mellitus: a meta-analysis of 2248 cases.

Li YY, Gao W, Pang SS, Min XY, Yang ZJ, Wang H, Lu XZ, Wang LS, Wang XM, Qian Y, Zhou CW, Wu J, Chen AL. Li YY, et al. Among authors: wang h, wang xm, wang ls. J Cell Mol Med. 2014 May;18(5):929-37. doi: 10.1111/jcmm.12244. Epub 2014 Mar 21. J Cell Mol Med. 2014. PMID: 24655325 Free PMC article.

8

CHIP protects against MPP⁺/MPTP-induced damage by regulating Drp1 in two models of Parkinson's disease.

Hu Z, Mao C, Wang H, Zhang Z, Zhang S, Luo H, Tang M, Yang J, Yuan Y, Wang Y, Liu Y, Fan L, Zhang Q, Yao D, Liu F, Schisler JC, Shi C, Xu Y. Hu Z, et al. Among authors: wang h, wang y. Aging (Albany NY). 2021 Jan 2;13(1):1458-1472. doi: 10.18632/aging.202389. Epub 2021 Jan 2. Aging (Albany NY). 2021. PMID: 33472166 Free PMC article.

9

Association of the mutation for the human carboxypeptidase E gene exon 4 with the severity of coronary artery atherosclerosis.

Jia EZ, Wang J, Yang ZJ, Zhu TB, Wang LS, Wang H, Li CJ, Chen B, Cao KJ, Huang J, Ma WZ. Jia EZ, et al. Among authors: wang h, wang j, wang ls. Mol Biol Rep. 2009 Feb;36(2):245-54. doi: 10.1007/s11033-007-9173-4. Epub 2007 Dec 16. Mol Biol Rep. 2009. PMID: 18080843

10

PRISMA-combined Myeloperoxidase -463G/A gene polymorphism and coronary artery disease: A meta-analysis of 4744 subjects.

Li YY, Wang H, Qian J, Kim HJ, Wu JJ, Wang LS, Zhou CW, Yang ZJ, Lu XZ. Li YY, et al. Among authors: wang h, wang ls. Medicine (Baltimore). 2017 Mar;96(12):e6461. doi: 10.1097/MD.0000000000006461. Medicine (Baltimore). 2017. PMID: 28328864 Free PMC article.

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