HuGE Literature Finder
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| Cooperative participation of epigenomic and genomic alterations in the clinicopathological diversity of gastric adenocarcinomas: significance of cell adhesion and epithelial-mesenchymal transition-related signaling pathways. Carcinogenesis 2020 Jul . Yang Menghan, Arai Eri, Takahashi Yoriko, Totsuka Hirohiko, Chiku Suenori, Taniguchi Hirokazu, Katai Hitoshi, Sakamoto Hiromi, Yoshida Teruhiko, Kanai Y |
| RAS/RAF mutations and their associations with epigenetic alterations for distinct pathways in Vietnamese colorectal cancer. Pathology, research and practice 2020 Feb 152898. Ta To Van, Nguyen Quang Ngoc, Chu Ha Hoang, Truong Van-Long, Vuong Linh Di |
| DNA variants in Helicobacter pylori infected patients with chronic gastritis, dysplasia and gastric cancer. Advances in medical sciences 2019 Mar 64 (1): 79-84. Hnatyszyn Andrzej, Szalata Marlena, Skrzypczak-Zielinska Marzena, Wielgus Karolina, Stanczyk Jerzy, Dziuba Ireneusz, Mikstacki Adam, Dobrowolska Agnieszka, Waszak Malgorzata, Hnatyszyn Piotr Tomasz, Slomski Rysza |
| Molecular subtyping of gastric cancer combining genetic and epigenetic anomalies provides distinct clinicopathological features and prognostic impacts. Human mutation 2019 Mar 40 (3): 347-354. Tahara Tomomitsu, Tahara Sayumi, Horiguchi Noriyuki, Okubo Masaaki, Terada Tsuyoshi, Yamada Hyuga, Yoshida Dai, Omori Takafumi, Osaki Hayato, Maeda Kohei, Kamano Toshiaki, Funasaka Kohei, Nagasaka Mitsuo, Nakagawa Yoshihito, Shibata Tomoyuki, Ohmiya Nao |
| Epigenetic silencing of MLH1 in endometrial cancers is associated with larger tumor volume, increased rate of lymph node positivity and reduced recurrence-free survival. Gynecologic oncology 2017 09 146 (3): 588-595. Cosgrove Casey M, Cohn David E, Hampel Heather, Frankel Wendy L, Jones Dan, McElroy Joseph P, Suarez Adrian A, Zhao Weiqiang, Chen Wei, Salani Ritu, Copeland Larry J, O'Malley David M, Fowler Jeffrey M, Yilmaz Ahmet, Chassen Alexis S, Pearlman Rachel, Goodfellow Paul J, Backes Floor |
| Association between genetic polymorphisms in DNA mismatch repair-related genes with risk and prognosis of head and neck squamous cell carcinoma. International journal of cancer. Journal international du cancer 2015 Aug 137 (4): 810-8. Nogueira Guilherme Augusto Silva, Lourenço Gustavo Jacob, Oliveira Camila Borges Martins, Marson Fernando Augusto Lima, Lopes-Aguiar Leisa, Costa Ericka Francislaine Dias, Lima Tathiane Regine Penna, Liutti Vitor Teixeira, Leal Frederico, Santos Vivian Castro Antunes, Rinck-Junior José Augusto, Lima Carmen Silvia Pass |
| Microsatellite instability in gallbladder carcinoma. Virchows Archiv : an international journal of pathology 2015 Apr 466 (4): 393-402. Moy Andrea P, Shahid Mohammad, Ferrone Cristina R, Borger Darrell R, Zhu Andrew X, Ting David, Deshpande Vikr |
| Immunophenotypic analysis of ovarian endometrioid adenocarcinoma: correlation with KRAS mutation and the presence of endometriosis. Pathology 2013 Oct 45 (6): 559-66. Stewart Colin J R, Walsh Michael D, Budgeon Charley A, Crook Maxine L, Buchanan Daniel |
| Sperm DNA integrity and meiotic behavior assessment in an infertile male carrier of a 9qh+++ polymorphism. Journal of biomedicine & biotechnology 2011 1 2011 730847. García-Peiró A, Oliver-Bonet M, Navarro J, Abad C, Guitart M, Amengual M J, Benet |
| Taiwan hospital-based detection of Lynch syndrome distinguishes 2 types of microsatellite instabilities in colorectal cancers. Surgery 2010 1 147 (5): 720-8. Chang Shih-Ching, Lin Pei-Ching, Yang Shung-Haur, Wang Huann-Sheng, Liang Wen-Yih, Lin Jen-K |
| Topographic molecular profile of pheochromocytomas: role of somatic down-regulation of mismatch repair. The Journal of clinical endocrinology and metabolism 2006 1 91 (3): 1150-8. Blanes Alfredo, Sanchez-Carrillo Juan J, Diaz-Cano Salvador |
| Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA. Human mutation 2003 Dec 22 (6): 428-33. Taylor C F, Charlton R S, Burn J, Sheridan E, Taylor G |
| Analysis of the meiotic recombination gene REC8 for sequence variations in a population with severe male factor infertility. Systems biology in reproductive medicine 0 54 (3): 163-5. Griffin Jeanine, Emery Benjamin R, Christensen Greg L, Carrell Douglas |
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- Page last updated:Feb 03, 2023
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