Yuan L - Search Results

1

Genetic analysis of the RIC3 gene in Han Chinese patients with Parkinson's disease.

He D, Hu P, Deng X, Song Z, Yuan L, Yuan X, Deng H. He D, et al. Among authors: yuan x, yuan l. Neurosci Lett. 2017 Jul 13;653:351-354. doi: 10.1016/j.neulet.2017.06.007. Epub 2017 Jun 9. Neurosci Lett. 2017. PMID: 28606768

2

EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease.

Yuan L, Song Z, Xu H, Gu S, Zhu A, Gong L, Zhao Y, Deng H. Yuan L, et al. Neurosci Lett. 2013 May 24;543:69-71. doi: 10.1016/j.neulet.2013.02.056. Epub 2013 Apr 2. Neurosci Lett. 2013. PMID: 23562511

3

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: yuan l. 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

4

Molecular genetics of congenital nuclear cataract.

Deng H, Yuan L. Deng H, et al. Among authors: yuan l. Eur J Med Genet. 2014 Feb;57(2-3):113-22. doi: 10.1016/j.ejmg.2013.12.006. Epub 2013 Dec 30. Eur J Med Genet. 2014. PMID: 24384146 Review.

5

Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing.

Guo Y, Yuan J, Liang H, Xiao J, Xu H, Yuan L, Gao K, Wu B, Tang Y, Li X, Deng H. Guo Y, et al. Among authors: yuan j, yuan l. Mol Biol Rep. 2014 Jun;41(6):3631-5. doi: 10.1007/s11033-014-3227-1. Epub 2014 Feb 13. Mol Biol Rep. 2014. PMID: 24522658

6

Genetic variants and animal models in SNCA and Parkinson disease.

Deng H, Yuan L. Deng H, et al. Among authors: yuan l. Ageing Res Rev. 2014 May;15:161-76. doi: 10.1016/j.arr.2014.04.002. Epub 2014 Apr 21. Ageing Res Rev. 2014. PMID: 24768741 Review.

7

Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencing.

Guo Y, Yuan L, Yi J, Xiao J, Xu H, Lv H, Xiong W, Zheng W, Guan L, Zhang J, Xiang H, Qi Y, Deng H. Guo Y, et al. Among authors: yuan l. Indian J Biochem Biophys. 2013 Aug;50(4):253-8. Indian J Biochem Biophys. 2013. PMID: 24772942

8

Identification of a novel PHEX mutation in a Chinese family with X-linked hypophosphatemic rickets using exome sequencing.

Yuan L, Wu S, Xu H, Xiao J, Yang Z, Xia H, Liu A, Hu P, Lu A, Chen Y, Xu F, Deng H. Yuan L, et al. Biol Chem. 2015 Jan;396(1):27-33. doi: 10.1515/hsz-2014-0187. Biol Chem. 2015. PMID: 25060345

9

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: yuan l. 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

10

Identification of a Premature Termination Mutation in the Proline-Rich Transmembrane Protein 2 Gene in a Chinese Family with Febrile Seizures.

Zheng W, Zhang J, Deng X, Xiao J, Yuan L, Yang Y, Guan L, Song Z, Yang Z, Deng H. Zheng W, et al. Among authors: yuan l. Mol Neurobiol. 2016 Mar;53(2):835-841. doi: 10.1007/s12035-014-9047-4. Epub 2014 Dec 15. Mol Neurobiol. 2016. PMID: 25502464

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