Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 37 Records) |
| Query Trace: Neoplasms and FHIT[original query] |
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| Genetic polymorphisms of methylenetetrahydrofolate reductase and promoter methylation of MGMT and FHIT genes in diffuse large B cell lymphoma risk in Middle East. Annals of hematology 2007 Dec 86 (12): 887-95. Siraj Abdul K, Ibrahim Muna, Al-Rasheed Maha, Bu Rong, Bavi Prashant, Jehan Zeenath, Abubaker Jehad, Murad Walid, Al-Dayel Fouad, Ezzat Adnan, El-Solh Hassan, Uddin Shahab, Al-Kuraya Khaw |
| Lack of association of fragile histidine triad (FHIT) polymorphisms with lung cancer in the Korean population. Journal of human genetics 2007 52 (8): 668-74. Jung Hae-Yun, Sung Jae Sook, Whang Young Mi, Shin Hyoung Doo, Park Byung Lae, Kim Jun Suk, Shin Sang Won, Seo Hee Yun, Sung Hwa Jung, Choi In Keun, Oh Sang Cheul, Seo Jae Hong, Kim Yeul Ho |
| Strong signature of natural selection within an FHIT intron implicated in prostate cancer risk. PloS one 2008 3 (10): e3533. Ding Yan, Larson Garrett, Rivas Guillermo, Lundberg Cathryn, Geller Louis, Ouyang Ching, Weitzel Jeffrey, Archambeau John, Slater Jerry, Daly Mary B, Benson Al B, Kirkwood John M, O'Dwyer Peter J, Sutphen Rebecca, Stewart James A, Johnson David, Nordborg Magnus, Krontiris Theodore |
| Mutation analysis of the FHIT gene in bronchoscopic specimens from patients with suspected lung cancer. Tumori 0 94 (6): 845-8. Cecener Gulsah, Tunca Berrin, Egeli Unal, Karadag Mehmet, Vatan Ozgur, Uzaslan Esra, Tolunay Sahsi |
| 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 |
| Homozygous deletion but not mutation of exons 5 and 8 of the fragile histidine triad (FHIT) gene is associated with features of differentiated thyroid carcinoma. Annals of clinical and laboratory science 2010 40 (3): 267-72. Yin De-Tao, Wang Lin, Sun Jianrei, Yin Fengyan, Yan Qingtao, Shen Ru-Long, Gao Jian-Xin, He Ga |
| Mutational and promoter hypermethylation status of FHIT gene in breast cancer patients of Kashmir. Mutation research 2011 Feb 707 (1-2): 1-8. Syeed Nidda, Husain Syed Akhtar, Sameer A Syed, Chowdhri Nissar A, Siddiqi Mushtaq |
| Inverse correlation between EGFR mutation and FHIT, RASSF1A and RUNX3 methylation in lung adenocarcinoma: relation with smoking status. Anticancer research 2011 Apr 31 (4): 1211-4. Yanagawa Naoki, Tamura Gen, Oizumi Hiroyuki, Endoh Makoto, Sadahiro Mitsuaki, Motoyama Teiic |
| Genome-wide disease association study in chewing tobacco associated oral cancers. Oral oncology 2012 Sep 48 (9): 831-5. Bhatnagar Renu, Dabholkar Jyoti, Saranath Dhananja |
| A clinical-biological risk stratification model for resected gastric cancer: prognostic impact of Her2, Fhit, and APC expression status. Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2013 Mar 24 (3): 693-701. Bria E, De Manzoni G, Beghelli S, Tomezzoli A, Barbi S, Di Gregorio C, Scardoni M, Amato E, Frizziero M, Sperduti I, Corbo V, Brunelli M, Bersani S, Tortora G, Scarpa |
| Diagnostic value of the FHIT and p16 mRNA loss and the K-ras gene mutation in pleural fluids for malignant pleural effusion. Cancer biomarkers : section A of Disease markers 2013 13 (1): 49-58. Li Jian, Bao Qian-Lei, Wang Yi, Hu Yi-Ming, Chen Pi |
| 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 |
| Significant frequency of allelic imbalance in 3p region covering RARß and MLH1 loci seems to be essential in molecular non-small cell lung cancer diagnosis. Medical oncology (Northwood, London, England) 2013 Jun 30 (2): 532. Antczak Adam, Migdalska-S?k Monika, Pastuszak-Lewandoska Dorota, Czarnecka Karolina, Nawrot Ewa, Doma?ska Daria, Kordiak Jacek, Górski Pawe?, Brzezia?ska E |
| 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 |
| Copy number variability analysis of pharmacogenes in patients with lymphoma, leukemia, hepatocellular, and lung carcinoma using The Cancer Genome Atlas data. Pharmacogenetics and genomics 2015 Jan 25 (1): 1-7. Kim In-Wha, Han Nayoung, Kim Myeong Gyu, Kim Therasa, Oh Jung |
| Genome-wide analysis of esophageal adenocarcinoma yields specific copy number aberrations that correlate with prognosis. Genes, chromosomes & cancer 2014 Apr 53 (4): 324-38. Frankel Adam, Armour Nicola, Nancarrow Derek, Krause Lutz, Hayward Nicholas, Lampe Guy, Smithers B Mark, Barbour Andr |
| Genome wide DNA copy number analysis in cholangiocarcinoma using high resolution molecular inversion probe single nucleotide polymorphism assay. Experimental and molecular pathology 2015 Aug 99 (2): 344-353. Arnold Alexander, Bahra Marcus, Lenze Dido, Bradtmöller Maren, Guse Katrin, Gehlhaar Claire, Bläker Hendrik, Heppner Frank L, Koch Are |
| Combined TP53 mutation/3p loss correlates with decreased radiosensitivity and increased matrix-metalloproteinase activity in head and neck carcinoma. Oral oncology 2015 Feb . Raju Sharat C, Hauff Samantha J, Lemieux Aaron J, Orosco Ryan K, Gross Andrew M, Nguyen Linda T, Savariar Elamprakash, Moss William, Whitney Michael, Cohen Ezra E, Lippman Scott M, Tsien Roger Y, Ideker Trey, Advani Sunil J, Nguyen Quyen |
| 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 |
| Comprehensive molecular portrait using next generation sequencing of resected intestinal-type gastric cancer patients dichotomized according to prognosis. Scientific reports 2016 6 22982. Bria E, Pilotto S, Simbolo M, Fassan M, de Manzoni G, Carbognin L, Sperduti I, Brunelli M, Cataldo I, Tomezzoli A, Mafficini A, Turri G, Karachaliou N, Rosell R, Tortora G, Scarpa |
Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer.
Nature communications 2017 Jul 8 15966. Son Ho-Young, Hwangbo Yul, Yoo Seong-Keun, Im Sun-Wha, Yang San Duk, Kwak Soo-Jung, Park Min Seon, Kwak Soo Heon, Cho Sun Wook, Ryu Jun Sun, Kim Jeongseon, Jung Yuh-Seog, Kim Tae Hyun, Kim Su-Jin, Lee Kyu Eun, Park Do Joon, Cho Nam Han, Sung Joohon, Seo Jeong-Sun, Lee Eun Kyung, Park Young Joo, Kim Jong- |
| Multiple single nucleotide polymorphism analysis and association of specific genotypes in FHIT, SAMD4A, and ANKRD17 in Indian patients with oral cancer. Head & neck 2017 Jun . D'Souza Wendy, Pradhan Sultan, Saranath Dhananja |
| 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 |
| Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development. Oncotarget 2019 Mar 10 (19): 1760-1774. Li Yafang, Xiao Xiangjun, Bossé Yohan, Gorlova Olga, Gorlov Ivan, Han Younghun, Byun Jinyoung, Leighl Natasha, Johansen Jakob S, Barnett Matt, Chen Chu, Goodman Gary, Cox Angela, Taylor Fiona, Woll Penella, Wichmann H Erich, Manz Judith, Muley Thomas, Risch Angela, Rosenberger Albert, Han Jiali, Siminovitch Katherine, Arnold Susanne M, Haura Eric B, Bolca Ciprian, Holcatova Ivana, Janout Vladimir, Kontic Milica, Lissowska Jolanta, Mukeria Anush, Ognjanovic Simona, Orlowski Tadeusz M, Scelo Ghislaine, Swiatkowska Beata, Zaridze David, Bakke Per, Skaug Vidar, Zienolddiny Shanbeh, Duell Eric J, Butler Lesley M, Houlston Richard, Artigas María Soler, Grankvist Kjell, Johansson Mikael, Shepherd Frances A, Marcus Michael W, Brunnström Hans, Manjer Jonas, Melander Olle, Muller David C, Overvad Kim, Trichopoulou Antonia, Tumino Rosario, Liu Geoffrey, Bojesen Stig E, Wu Xifeng, Le Marchand Loic, Albanes Demetrios, Bickeböller Heike, Aldrich Melinda C, Bush William S, Tardon Adonina, Rennert Gad, Teare M Dawn, Field John K, Kiemeney Lambertus A, Lazarus Philip, Haugen Aage, Lam Stephen, Schabath Matthew B, Andrew Angeline S, Bertazzi Pier Alberto, Pesatori Angela C, Christiani David C, Caporaso Neil, Johansson Mattias, McKay James D, Brennan Paul, Hung Rayjean J, Amos Christopher |
| A genome-wide association study identifies single nucleotide polymorphisms associated with time-to-metastasis in colorectal cancer.
BMC cancer 2019 Feb 19 (1): 133. Penney Michelle E, Parfrey Patrick S, Savas Sevtap, Yilmaz Yildiz |
| Genetic Analysis Reveals the Important Role of the APC Gene in Clear Cell Renal Cell Carcinoma. Anticancer research 2021 9 41 (9): 4295-4304. Lai Yen-Chein, Wang Wen-Chu |
| 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 |
| Genomic Landscape of Primary and Recurrent Anal Squamous Cell Carcinomas in Relation to HPV Integration, Copy-Number Variation, and DNA Damage Response Genes. Molecular cancer research : MCR 2021 4 19 (8): 1308-1321. Aldersley Jordan, Lorenz David R, Mouw Kent W, D'Andrea Alan D, Gabuzda Da |
| Genome-wide exploration of genetic interactions for bladder cancer risk. International journal of cancer 2023 8 . Evan Yi-Wen Yu, Qiu-Yi Tang, Ya-Ting Chen, Yan-Xi Zhang, Ya-Nan Dai, Yu-Xuan Wu, Wen-Chao Li, Siamak Mehrkanoon, Shi-Zhi Wang, Maurice P Zeegers, Anke Wesseli |
| Investigation of the IL7R? Gene Polymorphism rs6897932 and the Expression Levels of the CDH1, TTPAL, and FHIT Genes in Patients with Breast Cancer. Puerto Rico health sciences journal 2023 12 42 (4): 283-290. Evrim Suna Arikan-Soylemez, Murat Çilekar, Murat Akici, Çigdem Tokyol, Hatice Arzu Özyürek, Zafer Söylemez, Mustafa Sol |
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