Yang Z - Search Results

1

Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease.

Deng S, Deng X, Yuan L, Song Z, Yang Z, Xiong W, Deng H. Deng S, et al. Among authors: yang z. Acta Neurol Belg. 2015 Sep;115(3):267-71. doi: 10.1007/s13760-014-0347-2. Epub 2014 Aug 5. Acta Neurol Belg. 2015. PMID: 25092551

2

Genetic analysis of the S100B gene in Chinese patients with Parkinson disease.

Guo Y, Yang H, Deng X, Song Z, Yang Z, Xiong W, Yuan L, Xu H, Deng S, Deng H. Guo Y, et al. Among authors: yang h, yang z. Neurosci Lett. 2013 Oct 25;555:134-6. doi: 10.1016/j.neulet.2013.09.037. Epub 2013 Sep 25. Neurosci Lett. 2013. PMID: 24076007

3

Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia Congenita.

Huang X, Deng X, Xu H, Wu S, Yuan L, Yang Z, Yang Y, Deng H. Huang X, et al. Among authors: yang y, yang z. PLoS One. 2015 Jun 1;10(6):e0127529. doi: 10.1371/journal.pone.0127529. eCollection 2015. PLoS One. 2015. PMID: 26030151 Free PMC article.

4

Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease.

Yuan L, Deng X, Song Z, Yang Z, Ni B, Chen Y, Deng H. Yuan L, et al. Among authors: yang z. Neurobiol Aging. 2015 Oct;36(10):2907.e11-2. doi: 10.1016/j.neurobiolaging.2015.06.019. Epub 2015 Jun 19. Neurobiol Aging. 2015. PMID: 26163985

5

Identification of a Novel Mutation in the Titin Gene in a Chinese Family with Limb-Girdle Muscular Dystrophy 2J.

Zheng W, Chen H, Deng X, Yuan L, Yang Y, Song Z, Yang Z, Wu Y, Deng H. Zheng W, et al. Among authors: yang y, yang z. Mol Neurobiol. 2016 Oct;53(8):5097-102. doi: 10.1007/s12035-015-9439-0. Epub 2015 Sep 21. Mol Neurobiol. 2016. PMID: 26392295

6

TCEANC2 rs10788972 and rs12046178 variants in the PARK10 region in Chinese Han patients with sporadic Parkinson's disease.

Guo Y, Tan T, Deng X, Song Z, Yang Z, Yang Y, Deng H. Guo Y, et al. Among authors: yang y, yang z. Neurobiol Aging. 2015 Dec;36(12):3335.e1-3335.e2. doi: 10.1016/j.neurobiolaging.2015.09.002. Epub 2015 Sep 8. Neurobiol Aging. 2015. PMID: 26432391

7

Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson's disease patients.

Yuan L, Song Z, Deng X, Xiong W, Yang Z, Deng H. Yuan L, et al. Among authors: yang z. Neurosci Lett. 2016 Mar 11;616:26-31. doi: 10.1016/j.neulet.2016.01.031. Epub 2016 Jan 21. Neurosci Lett. 2016. PMID: 26806866

8

Genetic analysis of FGF20 variants in Chinese Han patients with essential tremor.

Yuan L, Song Z, Deng X, Zheng W, Yang Z, Yang Y, Deng H. Yuan L, et al. Among authors: yang y, yang z. Neurosci Lett. 2016 May 4;620:159-62. doi: 10.1016/j.neulet.2016.03.055. Epub 2016 Mar 31. Neurosci Lett. 2016. PMID: 27040428

9

Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease.

Yuan L, Song Z, Deng X, Zheng W, Guo Y, Yang Z, Deng H. Yuan L, et al. Among authors: yang z. Sci Rep. 2016 Sep 22;6:33850. doi: 10.1038/srep33850. Sci Rep. 2016. PMID: 27653456 Free PMC article.

10

Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson's Disease.

Yuan L, Song Z, Deng X, Yang Z, Yang Y, Guo Y, Lu H, Deng H. Yuan L, et al. Among authors: yang y, yang z. Neurosci Bull. 2017 Oct;33(5):510-514. doi: 10.1007/s12264-017-0122-5. Epub 2017 Mar 24. Neurosci Bull. 2017. PMID: 28341977 Free PMC article.

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