Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and FHIT[original query] |
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| Reduced Fhit protein expression and loss of heterozygosity at FHIT gene in tumours from smoking and asbestos-exposed lung cancer patients. International journal of oncology 2002 1 20 (2): 285-90. Pylkkanen Lea, Wolff Henrik, Stjernvall Tuula, Tuominen Paivi, Sioris Thanos, Karjalainen Antti, Anttila Sisko, Husgafvel-Pursiainen Kirs |
| Detection of HPV-DNA, p53 alterations, and methylation in penile squamous cell carcinoma in Japanese men. Pathology international 2008 Aug 58 (8): 477-82. Yanagawa Naoki, Osakabe Mitsumasa, Hayashi Masahiro, Tamura Gen, Motoyama Teiic |
| Gene mutations in esophageal mucosa of chagas disease patients. Anticancer research 2009 Apr 29 (4): 1243-7. DA Silva Manoel-Caetano Fernanda, Silveira Aparecida F P, Silva Ana Elizabe |
| A panel of sputum-based genomic marker for early detection of lung cancer. Cancer prevention research (Philadelphia, Pa.) 2010 Dec 3 (12): 1571-8. Jiang Feng, Todd Nevins W, Li Ruiyun, Zhang Howard, Fang Hongbin, Stass Sanford |
Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.
Translational psychiatry 2012 2 e129. Adkins D E, Clark S L, Åberg K, Hettema J M, Bukszár J, McClay J L, Souza R P, van den Oord E J C |
| Kras gene mutation and RASSF1A, FHIT and MGMT gene promoter hypermethylation: indicators of tumor staging and metastasis in adenocarcinomatous sporadic colorectal cancer in Indian population. PloS one 2013 8 (4): e60142. Sinha Rupal, Hussain Showket, Mehrotra Ravi, Kumar R Suresh, Kumar Kapil, Pande Pankaj, Doval Dinesh Chandra, Basir Seemi Farhat, Bharadwaj Mausu |
| Expanding the genetic basis of copy number variation in familial breast cancer. Hereditary cancer in clinical practice 2014 12 (1): 15. Masson Amy L, Talseth-Palmer Bente A, Evans Tiffany-Jane, Grice Desma M, Hannan Garry N, Scott Rodney |
| Integrated Genomic Analysis of Pancreatic Ductal Adenocarcinomas Reveals Genomic Rearrangement Events as Significant Drivers of Disease. Cancer research 2015 Dec . Murphy Stephen J, Hart Steven N, Halling Geoffrey, Johnson Sarah H, Smadbeck James B, Drucker Travis, Felipe Lima Joema, Rakhshan Rohakhtar Fariborz, Harris Faye R, Kosari Farhad, Subramanian Subbaya, Petersen Gloria M, Wiltshire Timothy D, Kipp Benjamin R, Truty Mark J, McWilliams Robert R, Couch Fergus J, Vasmatzis Geor |
| Response to interferon-beta treatment in multiple sclerosis patients: a genome-wide association study. The pharmacogenomics journal 2016 Mar . Mahurkar S, Moldovan M, Suppiah V, Sorosina M, Clarelli F, Liberatore G, Malhotra S, Montalban X, Antigüedad A, Krupa M, Jokubaitis V G, McKay F C, Gatt P N, Fabis-Pedrini M J, Martinelli V, Comi G, Lechner-Scott J, Kermode A G, Slee M, Taylor B V, Vandenbroeck K, Comabella M, Boneschi F M, , King |
| Genomic alterations of plasma cell-free DNAs in small cell lung cancer and their clinical relevance. Lung cancer (Amsterdam, Netherlands) 2018 Jun 120 113-121. Du Meijun, Thompson Jonathan, Fisher Hannah, Zhang Peng, Huang Chiang-Ching, Wang Lia |
| Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population.
Scientific reports 2018 Mar 8 (1): 4356. Zhou Sirui, Gan-Or Ziv, Ambalavanan Amirthagowri, Lai Dongbing, Xie Pingxing, Bourassa Cynthia V, Strong Stephanie, Ross Jay P, Dionne-Laporte Alexandre, Spiegelman Dan, Dupré Nicolas, Foroud Tatiana M, Xiong Lan, Dion Patrick A, Rouleau Guy |
| rs73092672 allele T is significantly associated with the higher risk of breast cancer incidence. Nucleosides, nucleotides & nucleic acids 2021 7 40 (8): 779-789. Oroujalian Andisheh, Peymani Maryam, Ghaedi Kamr |
- Page last reviewed:Feb 1, 2024
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