Zhang CE - Search Results

1

[HLA-G1 molecule expressed by ECV304 cells inhibit cytotoxic activity of allogeneic NK cells].

Zhang CE, Han JY, Yang HJ, Wu XW, Huang YF, Liang ZH, Gong FL. Zhang CE, et al. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2005 Nov;21(6):676-8. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2005. PMID: 16256023 Chinese.

2

Peptide-specific, allogeneic T cell response in vitro induced by a self-peptide binding to HLA-A2.

Weng X, Liang Z, Lu X, Zhong M, Lu S, Zhang C, Deng J, Wu X, Gong F. Weng X, et al. Sci China C Life Sci. 2007 Apr;50(2):203-11. doi: 10.1007/s11427-007-0036-y. Sci China C Life Sci. 2007. PMID: 17447027

3

A simplified PCR-SSP method for HLA-A2 subtype in a population of Wuhan, China.

Liang B, Zhu L, Liang Z, Weng X, Lu X, Zhang C, Li H, Wu X. Liang B, et al. Cell Mol Immunol. 2006 Dec;3(6):453-8. Cell Mol Immunol. 2006. PMID: 17257499 Free article.

4

Induction of the Epstein-Barr virus latent membrane protein 2 antigen-specific cytotoxic T lymphocytes using human leukocyte antigen tetramer-based artificial antigen-presenting cells.

Lu XL, Liang ZH, Zhang CE, Lu SJ, Weng XF, Wu XW. Lu XL, et al. Among authors: zhang ce. Acta Biochim Biophys Sin (Shanghai). 2006 Mar;38(3):157-63. doi: 10.1111/j.1745-7270.2006.00150.x. Acta Biochim Biophys Sin (Shanghai). 2006. PMID: 16518539 Free article.

5

Linkage of a locus determining familial progressive hyperpigmentation (FPH) to chromosome 19p13.1-pter in a Chinese family.

Zhang C, Deng Y, Chen X, Wu X, Jin W, Li H, Yu C, Xiong Y, Zhou L, Chen Y. Zhang C, et al. Eur J Dermatol. 2006 May-Jun;16(3):246-50. Eur J Dermatol. 2006. PMID: 16709486

6

Mutations in ABCB6 cause dyschromatosis universalis hereditaria.

Zhang C, Li D, Zhang J, Chen X, Huang M, Archacki S, Tian Y, Ren W, Mei A, Zhang Q, Fang M, Su Z, Yin Y, Liu D, Chen Y, Cui X, Li C, Yang H, Wang Q, Wang J, Liu M, Deng Y. Zhang C, et al. J Invest Dermatol. 2013 Sep;133(9):2221-8. doi: 10.1038/jid.2013.145. Epub 2013 Mar 21. J Invest Dermatol. 2013. PMID: 23519333 Free article.

7

Four novel mutations of ADAR1 in Chinese patients with dyschromatosis symmetrica hereditaria.

Hu W, Shi X, Li H, Chen L, Wang T, Dong Y, Zhang Y, Hu M, Liu X, Zhang C, Liu D, Deng Y. Hu W, et al. Indian J Dermatol Venereol Leprol. 2019 Jan-Feb;85(1):69-73. doi: 10.4103/ijdvl.IJDVL_66_17. Indian J Dermatol Venereol Leprol. 2019. PMID: 29536976 Free article.

8

Dysregulation of mTOR signalling is a converging mechanism in lissencephaly.

Zhang C, Liang D, Ercan-Sencicek AG, Bulut AS, Cortes J, Cheng IQ, Henegariu O, Nishimura S, Wang X, Peksen AB, Takeo Y, Caglar C, Lam TT, Koroglu MN, Narayanan A, Lopez-Giraldez F, Miyagishima DF, Mishra-Gorur K, Barak T, Yasuno K, Erson-Omay EZ, Yalcinkaya C, Wang G, Mane S, Kaymakcalan H, Guzel A, Caglayan AO, Tuysuz B, Sestan N, Gunel M, Louvi A, Bilguvar K. Zhang C, et al. Nature. 2025 Jan 1. doi: 10.1038/s41586-024-08341-9. Online ahead of print. Nature. 2025. PMID: 39743596

9

Investigating the landscape of immune-related genes and immunophenotypes in atherosclerosis: A bioinformatics Mendelian randomization study.

Zhang L, Wang C, Zhang C, Zhang L, Yang C, Zhang X. Zhang L, et al. Among authors: zhang c. Biochim Biophys Acta Mol Basis Dis. 2024 Dec 30;1871(3):167649. doi: 10.1016/j.bbadis.2024.167649. Online ahead of print. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 39740383 Free article.

10

The potential impact of inflammation on the lipid paradox in patients with acute myocardial infarction: a multicenter study.

Zeng G, Zhang C, Song Y, Zhang Z, Xu J, Liu Z, Tang X, Wang X, Chen Y, Zhang Y, Zhu P, Guo X, Jiang L, Wang Z, Liu R, Wang Q, Yao Y, Feng Y, Han Y, Yuan J. Zeng G, et al. Among authors: zhang c. BMC Med. 2024 Dec 23;22(1):599. doi: 10.1186/s12916-024-03823-z. BMC Med. 2024. PMID: 39710711 Free PMC article.

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