Chen C - Search Results

1

A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing.

Chen C, Lu CX, Wang Q, Cao LH, Luo Y, Zhang X. Chen C, et al. Genet Test Mol Biomarkers. 2016 Apr;20(4):203-7. doi: 10.1089/gtmb.2015.0248. Epub 2016 Feb 11. Genet Test Mol Biomarkers. 2016. PMID: 26866448

2

TERT promoter mutations lead to high transcriptional activity under hypoxia and temozolomide treatment and predict poor prognosis in gliomas.

Chen C, Han S, Meng L, Li Z, Zhang X, Wu A. Chen C, et al. PLoS One. 2014 Jun 17;9(6):e100297. doi: 10.1371/journal.pone.0100297. eCollection 2014. PLoS One. 2014. PMID: 24937153 Free PMC article.

3

Screening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients.

Chen C, Ma H, Zhang F, Chen L, Xing X, Wang S, Zhang X, Luo Y. Chen C, et al. Among authors: chen l. PLoS One. 2014 Sep 22;9(9):e108038. doi: 10.1371/journal.pone.0108038. eCollection 2014. PLoS One. 2014. PMID: 25244321 Free PMC article.

4

Intra-host dynamics of Ebola virus during 2014.

Ni M, Chen C, Qian J, Xiao HX, Shi WF, Luo Y, Wang HY, Li Z, Wu J, Xu PS, Chen SH, Wong G, Bi Y, Xia ZP, Li W, Lu HJ, Ma J, Tong YG, Zeng H, Wang SQ, Gao GF, Bo XC, Liu D. Ni M, et al. Among authors: chen sh, chen c. Nat Microbiol. 2016 Sep 5;1(11):16151. doi: 10.1038/nmicrobiol.2016.151. Nat Microbiol. 2016. PMID: 27595345

5

Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation.

Cao L, Yang W, Wang S, Chen C, Zhang X, Luo Y. Cao L, et al. Among authors: chen c. Genet Test Mol Biomarkers. 2017 Jun;21(6):357-362. doi: 10.1089/gtmb.2016.0415. Epub 2017 Apr 19. Genet Test Mol Biomarkers. 2017. PMID: 28422522

6

A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.

Cao L, Chen C, Leng Y, Yan L, Wang S, Zhang X, Luo Y. Cao L, et al. Among authors: chen c. J Genet. 2017 Sep;96(4):647-652. doi: 10.1007/s12041-017-0810-y. J Genet. 2017. PMID: 28947713

7

Mutations in mevalonate pathway genes in patients with familial or sporadic porokeratosis.

Leng Y, Yan L, Feng H, Chen C, Wang S, Luo Y, Cao L. Leng Y, et al. Among authors: chen c. J Dermatol. 2018 Jul;45(7):862-866. doi: 10.1111/1346-8138.14343. Epub 2018 May 3. J Dermatol. 2018. PMID: 29722423

8

A novel missense mutation of CRYGS underlies congenital cataract in a Chinese family.

Zhang T, Yan L, Leng Y, Chen C, Ma L, Wang Q, Zhang J, Cao L. Zhang T, et al. Among authors: chen c. Gene. 2018 Oct 30;675:9-14. doi: 10.1016/j.gene.2018.06.100. Epub 2018 Jun 28. Gene. 2018. PMID: 29964096

9

Short article: Sequence variations of PKHD1 underlie congenital hepatic fibrosis in a Chinese family.

Yang N, Leng Y, Dai S, Chen C, Liu C, Cao L. Yang N, et al. Among authors: chen c. Eur J Gastroenterol Hepatol. 2019 Mar;31(3):363-367. doi: 10.1097/MEG.0000000000001295. Eur J Gastroenterol Hepatol. 2019. PMID: 30507656

10

Cyclin G2 Inhibits the Warburg Effect and Tumour Progression by Suppressing LDHA Phosphorylation in Glioma.

Li S, Gao J, Zhuang X, Zhao C, Hou X, Xing X, Chen C, Liu Q, Liu S, Luo Y. Li S, et al. Among authors: chen c. Int J Biol Sci. 2019 Jan 1;15(3):544-555. doi: 10.7150/ijbs.30297. eCollection 2019. Int J Biol Sci. 2019. PMID: 30745841 Free PMC article.

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