Sun ZS - Search Results

1

Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility.

Bi C, Wu J, Jiang T, Liu Q, Cai W, Yu P, Cai T, Zhao M, Jiang YH, Sun ZS. Bi C, et al. Among authors: sun zs. Hum Mutat. 2012 Dec;33(12):1635-8. doi: 10.1002/humu.22174. Epub 2012 Aug 24. Hum Mutat. 2012. PMID: 22865819

2

Evolutionary mode and functional divergence of vertebrate NMDA receptor subunit 2 genes.

Teng H, Cai W, Zhou L, Zhang J, Liu Q, Wang Y, Dai W, Zhao M, Sun Z. Teng H, et al. PLoS One. 2010 Oct 14;5(10):e13342. doi: 10.1371/journal.pone.0013342. PLoS One. 2010. PMID: 20976280 Free PMC article.

3

Detection, annotation and visualization of alternative splicing from RNA-Seq data with SplicingViewer.

Liu Q, Chen C, Shen E, Zhao F, Sun Z, Wu J. Liu Q, et al. Genomics. 2012 Mar;99(3):178-82. doi: 10.1016/j.ygeno.2011.12.003. Epub 2011 Dec 28. Genomics. 2012. PMID: 22226708 Free article.

4

Identification of a novel Cys146X mutation of SOD1 in familial amyotrophic lateral sclerosis by whole-exome sequencing.

Wu J, Shen E, Shi D, Sun Z, Cai T. Wu J, et al. Genet Med. 2012 Sep;14(9):823-6. doi: 10.1038/gim.2012.50. Epub 2012 May 17. Genet Med. 2012. PMID: 22595939 Free article.

5

Regulation of peripheral clock to oscillation of substance P contributes to circadian inflammatory pain.

Zhang J, Li H, Teng H, Zhang T, Luo Y, Zhao M, Li YQ, Sun ZS. Zhang J, et al. Among authors: sun zs. Anesthesiology. 2012 Jul;117(1):149-60. doi: 10.1097/ALN.0b013e31825b4fc1. Anesthesiology. 2012. PMID: 22634872

6

Exome-assistant: a rapid and easy detection of disease-related genes and genetic variations from exome sequencing.

Liu Q, Shen E, Min Q, Li X, Wang X, Li X, Sun ZS, Wu J. Liu Q, et al. Among authors: sun zs. BMC Genomics. 2012 Dec 11;13:692. doi: 10.1186/1471-2164-13-692. BMC Genomics. 2012. PMID: 23231371 Free PMC article.

7

Genome-wide identification and divergent transcriptional expression of StAR-related lipid transfer (START) genes in teleosts.

Teng H, Cai W, Zeng K, Mao F, You M, Wang T, Zhao F, Sun Z. Teng H, et al. Gene. 2013 Apr 25;519(1):18-25. doi: 10.1016/j.gene.2013.01.058. Epub 2013 Feb 13. Gene. 2013. PMID: 23415839

8

New mutation in the SOD1 (copper/zinc superoxide dismutase-1) gene in a Chinese amyotrophic lateral sclerosis (ALS) patient.

Cui F, Cai W, Wang Z, Ren Y, Li M, Sun Z, Huang X. Cui F, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Dec;14(7-8):635-7. doi: 10.3109/21678421.2013.817589. Epub 2013 Jul 29. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23889606

9

Comparative RNA-seq analysis reveals potential mechanisms mediating the conversion to androgen independence in an LNCaP progression cell model.

Wang Y, Wang Y, Liu Q, Xu G, Mao F, Qin T, Teng H, Cai W, Yu P, Cai T, Zhao M, Sun ZS, Xie C. Wang Y, et al. Among authors: sun zs. Cancer Lett. 2014 Jan 1;342(1):130-8. doi: 10.1016/j.canlet.2013.08.044. Epub 2013 Sep 3. Cancer Lett. 2014. PMID: 24012641

10

Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.

Wang Z, Cai W, Cui F, Cai T, Chen Z, Mao F, Teng H, Chen L, Wang J, Sun Z, Huang X, Yu P. Wang Z, et al. Neurobiol Aging. 2014 Mar;35(3):725.e11-5. doi: 10.1016/j.neurobiolaging.2013.08.024. Epub 2013 Oct 1. Neurobiol Aging. 2014. PMID: 24094577

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