Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Syndrome and HCC[original query] |
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| Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in nonalcoholic chronic liver disease patients in India. Journal of gastroenterology and hepatology 2004 Jan 19 (1): 86-90. Thakur V, Guptan R C, Hashmi A Z, Sakhuja P, Malhotra V, Sarin S |
| GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation. Journal of hepatology 2012 Jan 56 (1): 184-91. Nault Jean Charles, Fabre Monique, Couchy Gabrielle, Pilati Camilla, Jeannot Emmanuelle, Tran Van Nhieu Jeanne, Saint-Paul Marie-Christine, De Muret Anne, Redon Marie-José, Buffet Catherine, Salenave Sylvie, Balabaud Charles, Prevot Sophie, Labrune Philippe, Bioulac-Sage Paulette, Scoazec Jean-Yves, Chanson Philippe, Zucman-Rossi Jessi |
| Mutational analysis of tumour suppressor gene NF2 in common solid cancers and acute leukaemias. Pathology 2012 Jan 44 (1): 29-32. Yoo Nam Jin, Park Sang Wook, Lee Sug Hyu |
| HCV-related liver and lymphoproliferative diseases: association with polymorphisms of IL28B and TLR2. Oncotarget 2016 May . De Re Valli, De Zorzi Mariangela, Caggiari Laura, Lauletta Gianfranco, Tornesello Maria Lina, Fognani Elisa, Miorin Marta, Racanelli Vito, Quartuccio Luca, Gragnani Laura, Russi Sabino, Pavone Fabio, Ghersetti Michela, Costa Elena Garlatti, Casarin Pietro, Bomben Riccardo, Mazzaro Cesare, Basaglia Giancarlo, Berretta Massimiliano, Vaccher Emanuela, Izzo Francesco, Buonaguro Franco Maria, De Vita Salvatore, Zignego Anna Linda, De Paoli Paolo, Dolcetti Riccar |
| High frequency of the PNPLA3 rs738409 [G] single-nucleotide polymorphism in Hmong individuals as a potential basis for a predisposition to chronic liver disease. Cancer 2018 Apr 124 Suppl 7 1583-1589. Tepper Clifford G, Dang Julie H T, Stewart Susan L, Fang Dao M, Wong Kimberly A, Liu Stephenie Y, Davis Ryan R, Dao Doan Y, Gregg Jeffrey P, Török Natalie J, Chen Moon |
| A non-synonymous polymorphism in NBS1 is associated with progression from chronic hepatitis B virus infection to hepatocellular carcinoma in a Chinese population. OncoTargets and therapy 2018 11 563-569. Zhen Ya'nan, Xiao Ruixue, Chen Xing, Yuan Changjin, Sun Yanlai, Li J |
| The Defective Allele of Aldehyde Dehydrogenase 2 Gene is Associated with Favorable Postoperative Prognosis in Hepatocellular Carcinoma. Journal of Cancer 2019 11 10 (23): 5735-5743. Huang Po-Han, Hu Ching-Chih, Chien Cheng-Hung, Chen Li-Wei, Chien Rong-Nan, Lin Yi-Shiuan, Chao Mei, Lin Chih-Lang, Yeh Chau-Ti |
| Nutrition and Genetics in NAFLD: The Perfect Binomium. International journal of molecular sciences 2020 Apr 21 (8): . Meroni Marica, Longo Miriam, Rustichelli Alice, Dongiovanni Pao |
| The effect of PNPLA3 polymorphism as gain in function mutation in the pathogenesis of non-alcoholic fatty liver disease. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2020 Feb 39 (1): 84-91. Delik An?l, Akk?z Hikmet, Dinçer Sad |
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