Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and LIG4[original query] |
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| Association between total immunoglobulin E and antibody responses to naturally acquired Ascaris lumbricoides infection and polymorphisms of immune system-related LIG4, TNFSF13B and IRS2 genes. Clinical and experimental immunology 2009 Aug 157 (2): 282-90. Acevedo N, Mercado D, Vergara C, Sánchez J, Kennedy M W, Jiménez S, Fernández A M, Gutiérrez M, Puerta L, Caraballo |
| Lung cancer susceptibility and prognosis associated with polymorphisms in the nonhomologous end-joining pathway genes: a multiple genotype-phenotype study. Cancer 2009 Jul 115 (13): 2939-48. Tseng Ruo-Chia, Hsieh Feng-Jen, Shih Chuen-Ming, Hsu Han-Shui, Chen Chih-Yi, Wang Yi-Chi |
| The role of common variants of non-homologous end-joining repair genes XRCC4, LIG4 and Ku80 in thyroid cancer risk. Oncology reports 2010 Oct 24 (4): 1079-85. Gomes Bruno Costa, Silva Susana Nunes, Azevedo Ana Paula, Manita Isabel, Gil Octávia Monteiro, Ferreira Teresa Cruz, Limbert Edward, Rueff José, Gaspar Jorge Francis |
| DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome. Cancer epidemiology 2012 Apr 36 (2): 183-9. Reeves Stuart G, Meldrum Cliff, Groombridge Claire, Spigelman Allan, Suchy Janina, Kurzawski Grzegorz, Lubinski Jan, Scott Rodney |
| Polymorphisms in DNA-repair genes in a cohort of prostate cancer patients from different areas in Spain: heterogeneity between populations as a confounding factor in association studies. PloS one 2013 8 (7): e69735. Henríquez-Hernández Luis Alberto, Valenciano Almudena, Foro-Arnalot Palmira, Alvarez-Cubero María Jesús, Cozar José Manuel, Suárez-Novo José Francisco, Castells-Esteve Manel, Ayala-Gil Adriana, Fernández-Gonzalo Pablo, Ferrer Montse, Guedea Ferrán, Sancho-Pardo Gemma, Craven-Bartle Jordi, Ortiz-Gordillo María José, Cabrera-Roldán Patricia, Herrera-Ramos Estefanía, Lara Pedro |
| Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity. Haematologica 2015 Jan 100 (1): 42-8. Zhang Michael Y, Keel Siobán B, Walsh Tom, Lee Ming K, Gulsuner Suleyman, Watts Amanda C, Pritchard Colin C, Salipante Stephen J, Jeng Michael R, Hofmann Inga, Williams David A, Fleming Mark D, Abkowitz Janis L, King Mary-Claire, Shimamura Aki |
| Polymorphisms in double strand break repair related genes influence radiosensitivity phenotype in lymphocytes from healthy individuals. DNA repair 2016 Mar 40 27-34. Mumbrekar Kamalesh Dattaram, Goutham Hassan Venkatesh, Vadhiraja Bejadi Manjunath, Bola Sadashiva Satish R |
| [Phenotypic and genetic analysis of four patients with 13q33-q34 microdeletion]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2017 8 34 (4): 509-513. Wang Huanhuan, Xiao Bing, Ji Xing, Zhang Jingmin, Cao Ying, Ni Lin, Ye Hui, Shen Lixi |
| Whole exome sequencing in unclassified autoinflammatory diseases: more monogenic diseases in the pipeline? Rheumatology (Oxford, England) 2020 5 60 (2): 607-616. Kosukcu Can, Taskiran Ekim Z, Batu Ezgi Deniz, Sag Erdal, Bilginer Yelda, Alikasifoglu Mehmet, Ozen Se |
| Characterization of a Cohort of Patients With LIG4 Deficiency Reveals the Founder Effect of p.R278L, Unique to the Chinese Population. Frontiers in immunology 2021 10 12 695993. Luo Xianze, Liu Qing, Jiang Jinqiu, Tang Wenjing, Ding Yuan, Zhou Lina, Yu Jie, Tang Xuemei, An Yunfei, Zhao Xiaodo |
| DNA Double-Strand Break Response and Repair Gene Polymorphisms May Influence Therapy Results and Prognosis in Head and Neck Cancer Patients. Cancers 2023 10 15 (20): . Dorota Butkiewicz, Ma?gorzata Krze?niak, Agnieszka Gdowicz-K?osok, Krzysztof Sk?adowski, Tomasz Rutkows |
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