Zhang S - Search Results

1

T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.

Zhang S, Wang L, Hao Y, Wang P, Hao P, Yin K, Wang QK, Liu M. Zhang S, et al. Mitochondrion. 2008 Jun;8(3):205-10. doi: 10.1016/j.mito.2008.02.003. Epub 2008 Mar 6. Mitochondrion. 2008. PMID: 18440284

2

Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family.

Zhang S, Liu M, Dong JM, Yin K, Wang P, Bu J, Li J, Hao YS, Hao P, Wang QK, Wang L. Zhang S, et al. Mol Vis. 2008;14:1893-7. Epub 2008 Oct 22. Mol Vis. 2008. PMID: 18958302 Free PMC article.

3

Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.

Zhang S, Yin K, Ren X, Wang P, Zhang S, Cheng L, Yang J, Liu JY, Liu M, Wang QK. Zhang S, et al. BMC Med Genet. 2008 Apr 9;9:24. doi: 10.1186/1471-2350-9-24. BMC Med Genet. 2008. PMID: 18400097 Free PMC article.

4

Mutation c.359_363delGTATTinsATAC in the COL4A5 causes Alport syndrome in a Chinese family.

Wang Q, Liu F, Xing Y, Wei X, Li H, Zhang S, Liu J, Wang Q, Tang Z, Liu M. Wang Q, et al. Among authors: zhang s. Gene. 2013 Jan 10;512(2):482-5. doi: 10.1016/j.gene.2012.10.014. Epub 2012 Oct 18. Gene. 2013. PMID: 23085274 Clinical Trial.

5

Ser217Cys mutation in the Ig II domain of FGFR3 in a Chinese family with autosomal dominant achondroplasia.

Zhang SR, Zhou XQ, Ren X, Wang TT, Yuan MX, Wang Q, Liu JY, Liu MG. Zhang SR, et al. Chin Med J (Engl). 2007 Jun 5;120(11):1017-9. Chin Med J (Engl). 2007. PMID: 17624273 No abstract available.

6

Frequent germline mutation in the BRCA2 gene in esophageal squamous cell carcinoma patients from a low-risk Chinese population.

Zhong L, Zhu ZZ, Shen Y, Sun G, Zhao X, Zhang S, Yin X, Zhu J, Xu Z, Zhu G. Zhong L, et al. Among authors: zhang s. Asian Pac J Cancer Prev. 2011;12(7):1771-6. Asian Pac J Cancer Prev. 2011. PMID: 22126563 Free article.

7

PATL2 mutations affect human oocyte maternal mRNA homeostasis and protein interactions in cell cycle regulation.

Zhang YL, Hu Z, Jiang H, Jin J, Zhou Y, Lai M, Ren P, Liu S, Zhang YY, Rong Y, Zheng W, Zhang S, Tong X, Zhang S. Zhang YL, et al. Among authors: zhang s. Cell Biosci. 2024 Dec 31;14(1):157. doi: 10.1186/s13578-024-01341-2. Cell Biosci. 2024. PMID: 39741299

8

LncRNA LUCAT1 offers protection against human coronary artery endothelial cellular oxidative stress injury through modulating hsa-miR-6776-5p/LRRC25 axis and activating autophagy flux.

Wang Y, Zhang X, Ren M, He S, Bie H, Duan M, Chen Z, Jia Q, Chi B, Gan X, Li C, Fu Y, Zhou H, Zhang S, Zhang Q, An F, Chen X, Jia E. Wang Y, et al. Among authors: zhang s. J Transl Med. 2024 Dec 31;22(1):1171. doi: 10.1186/s12967-024-05966-2. J Transl Med. 2024. PMID: 39741278

9

Electromagnetic metamaterial agent.

Hu S, Li M, Xu J, Zhang H, Zhang S, Cui TJ, Del Hougne P, Li L. Hu S, et al. Among authors: zhang s. Light Sci Appl. 2025 Jan 1;14(1):12. doi: 10.1038/s41377-024-01678-w. Light Sci Appl. 2025. PMID: 39741131

10

Multispectral Integrated Black Arsenene Phototransistors for High-Resolution Imaging and Enhanced Secure Communication.

Han L, Zhang S, Tian S, Zhang L, Wei Y, Zhang K, Jiang M, He Y, Liu C, Tang W, He J, Shu H, Politano A, Chen X, Wang L. Han L, et al. Among authors: zhang s. ACS Nano. 2024 Dec 31. doi: 10.1021/acsnano.4c14512. Online ahead of print. ACS Nano. 2024. PMID: 39741115

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