Zhou Y - Search Results

1

A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family.

Li XH, Song C, Chen SQ, Zhou Y, Guo H, Zhou CL, Yang ZY, Liang YX, Wang YM. Li XH, et al. Among authors: zhou y, zhou cl. Chin Med J (Engl). 2007 May 5;120(9):834-7. Chin Med J (Engl). 2007. PMID: 17531128 No abstract available.

2

Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families.

Chen S, Song C, Guo H, Xu P, Huang W, Zhou Y, Sun J, Li CX, Du Y, Li X, Liu Z, Geng D, Maxwell PH, Zhang C, Wang Y. Chen S, et al. Among authors: zhou y. Hum Mutat. 2005 Feb;25(2):135-41. doi: 10.1002/humu.20126. Hum Mutat. 2005. PMID: 15643603

3

Novel rare alleles of ABCA1 are exclusively associated with extreme high-density lipoprotein-cholesterol levels among the Han Chinese.

Hu S, Zhong Y, Hao Y, Luo M, Zhou Y, Guo H, Liao W, Wan D, Wei H, Gao Y, Shan J, Hu B, Hultén M, Wang Y. Hu S, et al. Among authors: zhou y. Clin Chem Lab Med. 2009;47(10):1239-45. doi: 10.1515/CCLM.2009.284. Clin Chem Lab Med. 2009. PMID: 19743957

4

Novel and known mutations of TGFBI, their genotype-phenotype correlation and structural modeling in 3 Chinese families with lattice corneal dystrophy.

Zhong X, Chen S, Huang W, Yang J, Chen X, Zhou Y, Zhou Q, Wang Y. Zhong X, et al. Among authors: zhou y, zhou q. Mol Vis. 2010 Feb 15;16:224-30. Mol Vis. 2010. PMID: 20161820 Free PMC article.

5

A 4.6 kb genomic duplication on 20p12.2-12.3 is associated with brachydactyly type A2 in a Chinese family.

Su P, Ding H, Huang D, Zhou Y, Huang W, Zhong L, Vyse TJ, Wang Y. Su P, et al. Among authors: zhou y. J Med Genet. 2011 May;48(5):312-6. doi: 10.1136/jmg.2010.084814. Epub 2011 Feb 26. J Med Genet. 2011. PMID: 21357617

6

Novel mutations of EXT1 and EXT2 genes among families and sporadic cases with multiple exostoses.

Pei Y, Wang Y, Huang W, Hu B, Huang D, Zhou Y, Su P. Pei Y, et al. Among authors: zhou y. Genet Test Mol Biomarkers. 2010 Dec;14(6):865-72. doi: 10.1089/gtmb.2010.0040. Epub 2010 Nov 1. Genet Test Mol Biomarkers. 2010. PMID: 21039224

7

Structure prediction of membrane proteins.

Zhou C, Zheng Y, Zhou Y. Zhou C, et al. Among authors: zhou y. Genomics Proteomics Bioinformatics. 2004 Feb;2(1):1-5. doi: 10.1016/s1672-0229(04)02001-7. Genomics Proteomics Bioinformatics. 2004. PMID: 15629037 Free PMC article. Review.

8

Age at onset-dependent presentations of premature hip osteoarthritis, avascular necrosis of the femoral head, or Legg-Calvé-Perthes disease in a single family, consequent upon a p.Gly1170Ser mutation of COL2A1.

Su P, Li R, Liu S, Zhou Y, Wang X, Patil N, Mow CS, Mason JC, Huang D, Wang Y. Su P, et al. Among authors: zhou y. Arthritis Rheum. 2008 Jun;58(6):1701-6. doi: 10.1002/art.23491. Arthritis Rheum. 2008. PMID: 18512791 Free article.

9

Association of -27T>C and its haplotype at the putative promoter for IgA-specific receptor gene with IgA nephropathy among the Chinese Han population.

Huang W, Gu H, Li R, Lou T, Zhang J, Shi W, Ye Z, Zhou Y, Li C, Xiong S, Li L, Wu C, Leung JC, Lam MF, Lai KN, Wang Y. Huang W, et al. Among authors: zhou y. Nephrol Dial Transplant. 2011 Aug;26(8):2537-44. doi: 10.1093/ndt/gfq765. Epub 2011 Jan 27. Nephrol Dial Transplant. 2011. PMID: 21273231

10

Database and analyses of known alternatively spliced genes in plants.

Zhou Y, Zhou C, Ye L, Dong J, Xu H, Cai L, Zhang L, Wei L. Zhou Y, et al. Among authors: zhou c. Genomics. 2003 Dec;82(6):584-95. doi: 10.1016/s0888-7543(03)00204-0. Genomics. 2003. PMID: 14611800

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