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For: Kawaguchi M, Yamamoto K, Takeda N, Fukushima T, Yamashita F, Sato K, Kitamura K, Hippo Y, Janetka JW, Kataoka H. Hepatocyte growth factor activator inhibitor-2 stabilizes Epcam and maintains epithelial organization in the mouse intestine. Commun Biol 2019;2:11. [PMID: 30623107 DOI: 10.1038/s42003-018-0255-8] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Szabo R, Bugge TH. Membrane-anchored serine proteases as regulators of epithelial function. Biochem Soc Trans 2020;48:517-28. [PMID: 32196551 DOI: 10.1042/BST20190675] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
2 Mukai S, Yamasaki K, Fujii M, Nagai T, Terada N, Kataoka H, Kamoto T. Dysregulation of Type II Transmembrane Serine Proteases and Ligand-Dependent Activation of MET in Urological Cancers. Int J Mol Sci 2020;21:E2663. [PMID: 32290402 DOI: 10.3390/ijms21082663] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
3 Prasad H, Visweswariah SS. Impaired Intestinal Sodium Transport in Inflammatory Bowel Disease: From the Passenger to the Driver's Seat. Cell Mol Gastroenterol Hepatol 2021;12:277-92. [PMID: 33744482 DOI: 10.1016/j.jcmgh.2021.03.005] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Gires O, Pan M, Schinke H, Canis M, Baeuerle PA. Expression and function of epithelial cell adhesion molecule EpCAM: where are we after 40 years? Cancer Metastasis Rev 2020;39:969-87. [PMID: 32507912 DOI: 10.1007/s10555-020-09898-3] [Cited by in Crossref: 25] [Cited by in F6Publishing: 23] [Article Influence: 25.0] [Reference Citation Analysis]
5 Wu CJ, Lu M, Feng X, Nakato G, Udey MC. Matriptase Cleaves EpCAM and TROP2 in Keratinocytes, Destabilizing Both Proteins and Associated Claudins. Cells 2020;9:E1027. [PMID: 32326212 DOI: 10.3390/cells9041027] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
6 Hatzold J, Wessendorf H, Pogoda HM, Bloch W, Hammerschmidt M. The Kunitz-type serine protease inhibitor Spint2 is required for cellular cohesion, coordinated cell migration and cell survival during zebrafish hatching gland development. Dev Biol 2021;476:148-70. [PMID: 33826923 DOI: 10.1016/j.ydbio.2021.03.017] [Reference Citation Analysis]
7 Kawaguchi M, Yamamoto K, Kataoka H, Izumi A, Yamashita F, Kiwaki T, Nishida T, Camerer E, Fukushima T. Protease-activated receptor-2 accelerates intestinal tumor formation through activation of nuclear factor-κB signaling and tumor angiogenesis in ApcMin/+ mice. Cancer Sci 2020;111:1193-202. [PMID: 31997435 DOI: 10.1111/cas.14335] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
8 Szabo R, Callies LK, Bugge TH. Matriptase drives early-onset intestinal failure in a mouse model of congenital tufting enteropathy. Development 2019;146:dev183392. [PMID: 31628112 DOI: 10.1242/dev.183392] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 3.7] [Reference Citation Analysis]
9 Xu Q, Ying P, Ren J, Kong N, Wang Y, Li YG, Yao Y, Kaplan DL, Ling S. Biomimetic Design for Bio-Matrix Interfaces and Regenerative Organs. Tissue Eng Part B Rev 2021;27:411-29. [PMID: 33138695 DOI: 10.1089/ten.TEB.2020.0234] [Reference Citation Analysis]
10 Das B, Sivagnanam M. Congenital Tufting Enteropathy: Biology, Pathogenesis and Mechanisms. J Clin Med 2020;10:E19. [PMID: 33374714 DOI: 10.3390/jcm10010019] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]