Li W - Search Results

1

Claudin-7 indirectly regulates the integrin/FAK signaling pathway in human colon cancer tissue.

Ding L, Wang L, Sui L, Zhao H, Xu X, Li T, Wang X, Li W, Zhou P, Kong L. Ding L, et al. Among authors: li t, li w. J Hum Genet. 2016 Aug;61(8):711-20. doi: 10.1038/jhg.2016.35. Epub 2016 Apr 28. J Hum Genet. 2016. PMID: 27121327

2

Severe Intestinal Inflammation in the Small Intestine of Mice Induced by Controllable Deletion of Claudin-7.

Li WJ, Xu C, Wang K, Li TY, Wang XN, Yang H, Xing T, Li WX, Chen YH, Gao H, Ding L. Li WJ, et al. Dig Dis Sci. 2018 May;63(5):1200-1209. doi: 10.1007/s10620-018-4973-z. Epub 2018 Feb 27. Dig Dis Sci. 2018. PMID: 29488037 Free PMC article.

3

Emerging clinical significance of claudin-7 in colorectal cancer: a review.

Wang K, Xu C, Li W, Ding L. Wang K, et al. Among authors: li w. Cancer Manag Res. 2018 Sep 20;10:3741-3752. doi: 10.2147/CMAR.S175383. eCollection 2018. Cancer Manag Res. 2018. PMID: 30288105 Free PMC article. Review.

4

Claudin-7 downregulation induces metastasis and invasion in colorectal cancer via the promotion of epithelial-mesenchymal transition.

Wang K, Li T, Xu C, Ding Y, Li W, Ding L. Wang K, et al. Among authors: li t, li w. Biochem Biophys Res Commun. 2019 Jan 15;508(3):797-804. doi: 10.1016/j.bbrc.2018.10.049. Epub 2018 Dec 6. Biochem Biophys Res Commun. 2019. PMID: 30528239

5

Claudin-7 gene knockout causes destruction of intestinal structure and animal death in mice.

Xu C, Wang K, Ding YH, Li WJ, Ding L. Xu C, et al. World J Gastroenterol. 2019 Feb 7;25(5):584-599. doi: 10.3748/wjg.v25.i5.584. World J Gastroenterol. 2019. PMID: 30774273 Free PMC article.

6

Non-tight junction-related function of claudin-7 in interacting with integrinβ1 to suppress colorectal cancer cell proliferation and migration.

Li W, Xu C, Wang K, Ding Y, Ding L. Li W, et al. Cancer Manag Res. 2019 Feb 13;11:1443-1451. doi: 10.2147/CMAR.S188020. eCollection 2019. Cancer Manag Res. 2019. PMID: 30863155 Free PMC article.

7

Clinical, genetic characteristics and outcome of four Chinese patients with Bartter syndrome type 3: Further insight into a genotype-phenotype correlation.

Piao Y, Chen C, Wu D, Liu M, Li W, Chen J, Sang Y. Piao Y, et al. Among authors: li w. Mol Genet Metab Rep. 2024 Jul 5;40:101112. doi: 10.1016/j.ymgmr.2024.101112. eCollection 2024 Sep. Mol Genet Metab Rep. 2024. PMID: 39071140 Free PMC article.

8

Long-term follow-up and mutation analysis of 27 chinese cases of congenital hyperinsulinism.

Su C, Gong C, Sanger P, Li W, Wu D, Gu Y, Cao B. Su C, et al. Among authors: li w. Horm Res Paediatr. 2014;81(3):169-76. doi: 10.1159/000356911. Epub 2014 Jan 9. Horm Res Paediatr. 2014. PMID: 24434300 Clinical Trial.

9

Clinical and Molecular Spectrum of Glutamate Dehydrogenase Gene Defects in 26 Chinese Congenital Hyperinsulinemia Patients.

Su C, Liang XJ, Li WJ, Wu D, Liu M, Cao BY, Chen JJ, Qin M, Meng X, Gong CX. Su C, et al. J Diabetes Res. 2018 Sep 16;2018:2802540. doi: 10.1155/2018/2802540. eCollection 2018. J Diabetes Res. 2018. PMID: 30306091 Free PMC article.

10

Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases.

Li W, Gong C, Qi Z, Wu DI, Cao B. Li W, et al. Exp Ther Med. 2015 Oct;10(4):1277-1282. doi: 10.3892/etm.2015.2677. Epub 2015 Aug 10. Exp Ther Med. 2015. PMID: 26622478 Free PMC article.

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