Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Neoplasms and ENG[original query] |
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| Development of a multicomponent prediction model for acute esophagitis in lung cancer patients receiving chemoradiotherapy. International journal of radiation oncology, biology, physics 2011 Oct 81 (2): 537-44. De Ruyck Kim, Sabbe Nick, Oberije Cary, Vandecasteele Katrien, Thas Olivier, De Ruysscher Dirk, Lambin Phillipe, Van Meerbeeck Jan, De Neve Wilfried, Thierens Hube |
| TGF-ß signaling pathway and breast cancer susceptibility. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 Jun 20 (6): 1112-9. Scollen Serena, Luccarini Craig, Baynes Caroline, Driver Kristy, Humphreys Manjeet K, Garcia-Closas Montserrat, Figueroa Jonine, Lissowska Jolanta, Pharoah Paul D, Easton Douglas F, Hesketh Robin, Metcalfe James C, Dunning Alison |
| Variation in telangiectasia predisposing genes is associated with overall radiation toxicity. International journal of radiation oncology, biology, physics 2012 Nov 84 (4): 1031-6. Tanteles George A, Murray Robert J S, Mills Jamie, Barwell Julian, Chakraborti Prabir, Chan Steve, Cheung Kwok-Leung, Ennis Dawn, Khurshid Nazish, Lambert Kelly, Machhar Rohan, Meisuria Mitul, Osman Ahmed, Peat Irene, Sahota Harjinder, Woodings Pamela, Talbot Christopher J, Symonds R Pa |
| Genetic polymorphism in a VEGF-independent angiogenesis gene ANGPT1 and overall survival of colorectal cancer patients after surgical resection. PloS one 2012 7 (4): e34758. Dai Jingyao, Wan Shaogui, Zhou Feng, Myers Ronald E, Guo Xu, Li Bingshan, Fu Xiaoying, Palazzo Juan P, Dou Kefeng, Yang Hushan, Xing Jinlia |
| ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment outcome of childhood acute lymphoblastic leukemia. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Mar 30 (7): 751-7. Xu Heng, Cheng Cheng, Devidas Meenakshi, Pei Deqing, Fan Yiping, Yang Wenjian, Neale Geoff, Scheet Paul, Burchard Esteban G, Torgerson Dara G, Eng Celeste, Dean Michael, Antillon Frederico, Winick Naomi J, Martin Paul L, Willman Cheryl L, Camitta Bruce M, Reaman Gregory H, Carroll William L, Loh Mignon, Evans William E, Pui Ching-Hon, Hunger Stephen P, Relling Mary V, Yang Jun |
| Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps. Gastroenterology 2013 Jun 144 (7): 1402-9, 1409.e1-5. Ngeow Joanne, Heald Brandie, Rybicki Lisa A, Orloff Mohammed S, Chen Jin Lian, Liu Xiuli, Yerian Lisa, Willis Joseph, Lehtonen Heli J, Lehtonen Rainer, Mester Jessica L, Moline Jessica, Burke Carol A, Church James, Aaltonen Lauri A, Eng Char |
| Germline variants in Hamartomatous Polyposis Syndrome-associated genes from patients with one or few hamartomatous polyps. Scandinavian journal of gastroenterology 2016 May 1-8. Jelsig Anne Marie, Brusgaard Klaus, Hansen Tine Plato, Qvist Niels, Larsen Martin, Bojesen Anders, Nielsen Claus Buhl, Ousager Lilian Bom |
| EIF1AX and NRAS Mutations Co-occur and Cooperate in Low-Grade Serous Ovarian Carcinomas. Cancer research 2017 Jun . Etemadmoghadam Dariush, Azar Walid J, Lei Ying, Moujaber Tania, Garsed Dale W, Kennedy Catherine, Fereday Sian, Mitchell Chris, Chiew Yoke-Eng, Hendley Joy, Group Australian Ovarian Cancer Study, Sharma Raghwa, Harnett Paul, Li Jason, Christie Elizabeth L, Patch Ann-Marie, George Joshy, Au-Yeung George, Mir Arnau Gisela, Holloway Timothy P, Semple Timothy, Pearson John V, Waddell Nicola, Grimmond Sean, Köbel Martin, Rizos Helen, Lomakin Ivan, Bowtell David D L, DeFazio An |
| Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort. Oncotarget 2017 12 8 (55): 93450-93463. Raskin Leon, Guo Yan, Du Liping, Clendenning Mark, Rosty Christophe, , Lindor Noralane M, Gruber Stephen B, Buchanan Daniel |
| Somatic and Germline Genomic Alterations in Very Young Women with Breast Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2022 2 28 (11): 2339-2348. Waks Adrienne G, Kim Dewey, Jain Esha, Snow Craig, Kirkner Gregory J, Rosenberg Shoshana M, Oh Coyin, Poorvu Philip D, Ruddy Kathryn J, Tamimi Rulla M, Peppercorn Jeffrey, Schapira Lidia, Borges Virginia F, Come Steven E, Brachtel Elena F, Warner Ellen, Collins Laura C, Partridge Ann H, Wagle Nikh |
| Genetic and molecular features of seizure-freedom following surgical resections for focal epilepsy: A pilot study. Frontiers in neurology 2022 10 13 942643. Louis Shreya, Busch Robyn M, Lal Dennis, Hockings Jennifer, Hogue Olivia, Morita-Sherman Marcia, Vegh Deborah, Najm Imad, Ghosh Chaitali, Bazeley Peter, Eng Charis, Jehi Lara, Rotroff Daniel |
| Changes in antioxidant status and DNA repair capacity are corroborated with molecular alterations in malignant thyroid tissue of patients with papillary thyroid cancer. Frontiers in molecular biosciences 2023 9 10 1237548. Zing Hong Eng, Azlina Abdul Aziz, Khoon Leong Ng, Sarni Mat Jun |
| Bioinformatics Analysis of the Genetic and Epigenetic Alterations of Bone Morphogenetic Protein Receptors in Metastatic Breast Cancer. Biochemical genetics 2023 7 . Adam Hermawan, Herwandhani Put |
| Rare germline variants in pancreatic cancer and multiple primary cancers: an autopsy study. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2023 3 . Fujitani Hiroo, Eguchi Hidetaka, Kochi Yuta, Arai Tomio, Muramatsu Masaaki, Okazaki Yasus |
| Whole-exome sequencing and bioinformatic analyses revealed differences in gene mutation profiles in papillary thyroid cancer patients with and without benign thyroid goitre background. Frontiers in endocrinology 2023 1 13 1039494. Eng Zing Hong, Abdullah Mardiaty Iryani, Ng Khoon Leong, Abdul Aziz Azlina, Arba'ie Nurul Hannis, Mat Rashid Nurullainy, Mat Junit Sar |
| Investigation of the Genetic Determinants of Telangiectasia and Solid Organ Arteriovenous Malformation Formation in Hereditary Hemorrhagic Telangiectasia (HHT). International journal of molecular sciences 2024 7 25 (14): . Kevin J Whitehead, Doruk Toydemir, Whitney Wooderchak-Donahue, Gretchen M Oakley, Bryan McRae, Angelica Putnam, Jamie McDonald, Pinar Bayrak-Toydem |
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