Human Genome Epidemiology Literature Finder
Records 1 - 29 (of 29 Records) |
Query Trace: ITGAV[original query] |
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The ITGAV rs3738919-C allele is associated with rheumatoid arthritis in the European Caucasian population: a family-based study. Arthritis research & therapy 2007 9 (4): R63. Jacq Laurent, Garnier Sophie, Dieudé Philippe, Michou Laëtitia, Pierlot Céline, Migliorini Paola, Balsa Alejandro, Westhovens René, Barrera Pilar, Alves Helena, Vaz Carlos, Fernandes Manuela, Pascual-Salcedo Dora, Bombardieri Stefano, Dequeker Jan, Radstake Timothy R, Van Riel Piet, van de Putte Leo, Lopes-Vaz Antonio, Glikmans Elodie, Barbet Sandra, Lasbleiz Sandra, Lemaire Isabelle, Quillet Patrick, Hilliquin Pascal, Teixeira Vitor Hugo, Petit-Teixeira Elisabeth, Mbarek Hamdi, Prum Bernard, Bardin Thomas, Cornélis François, |
Genetic polymorphisms associated with priapism in sickle cell disease. British journal of haematology 2007 May 137 (3): 262-7. Elliott Laine, Ashley-Koch Allison E, De Castro Laura, Jonassaint Jude, Price Jennifer, Ataga Kenneth I, Levesque Marc C, Brice Weinberg J, Eckman James R, Orringer Eugene P, Vance Jeffery M, Telen Marilyn |
Integrin alpha V polymorphisms and haplotypes in a Korean population are associated with susceptibility to chronic hepatitis and hepatocellular carcinoma. Liver international : official journal of the International Association for the Study of the Liver 2009 Feb 29 (2): 187-95. Lee Seung Ku, Kim Min-Ho, Cheong Jae Youn, Cho Sung Won, Yang Song-Ju, Kwack Kyub |
Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer: ITGB4 as prognostic marker. Carcinogenesis 2008 Jun . Brendle A, Lei H, Brandt A, Johansson R, Enquist K, Henriksson R, Hemminki K, Lenner P, Försti A |
The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets. Arthritis research & therapy 2009 11 (5): R152. Hollis-Moffatt Jade E, Rowley Kerry A, Phipps-Green Amanda J, Merriman Marilyn E, Dalbeth Nicola, Gow Peter, Harrison Andrew A, Highton John, Jones Peter B B, Stamp Lisa K, Harrison Pille, Wordsworth B Paul, Merriman Tony |
A polymorphism in the integrin aV subunit gene affects the progression of primary biliary cirrhosis in Japanese patients. Journal of gastroenterology 2011 May 46 (5): 676-86. Inamine Tatsuo, Nakamura Minoru, Kawauchi Ayumi, Shirakawa Yayoi, Hashiguchi Hisae, Aiba Yoshihiro, Taketomi Akinobu, Shirabe Ken, Nakamuta Makoto, Hayashi Shigeki, Saoshiro Takeo, Komori Atsumasa, Yatsuhashi Hiroshi, Kondo Shinji, Omagari Katsuhisa, Maehara Yoshihiko, Ishibashi Hiromi, Tsukamoto Kazuhiro, |
Identification of genes for bone mineral density variation by computational disease gene identification strategy. Journal of bone and mineral metabolism 2011 Nov 29 (6): 709-16. Li Gloria H Y, Deng Hong-Wen, Kung Annie W C, Huang Qing-Ya |
Genetic variants in the integrin gene predicted microRNA-binding sites were associated with the risk of prostate cancer. Molecular carcinogenesis 2012 Oct . Liu J, Huang J, He Y, Liu J, Liao B, Liao G |
An intron polymorphism of the fibronectin gene is associated with end-stage knee osteoarthritis in a Han Chinese population: two independent case-control studies. BMC musculoskeletal disorders 2014 15 (1): 173. Yang Hsin-Yi, Su Sui-Lung, Peng Yi-Jen, Wang Chih-Chien, Lee Herng-Sheng, Salter Donald M, Lee Chian-H |
Genetic Variation in Pattern Recognition Receptors and Adaptor Proteins Associated With Development of Chronic Q Fever. The Journal of infectious diseases 2015 Sep 212 (5): 818-29. Schoffelen Teske, Ammerdorffer Anne, Hagenaars Julia C J P, Bleeker-Rovers Chantal P, Wegdam-Blans Marjolijn C, Wever Peter C, Joosten Leo A B, van der Meer Jos W M, Sprong Tom, Netea Mihai G, van Deuren Marcel, van de Vosse Esth |
Genetic variations in the VEGF pathway as prognostic factors in metastatic colorectal cancer patients treated with oxaliplatin-based chemotherapy. The pharmacogenomics journal 2015 Oct 15 (5): 397-404. Paré-Brunet L, Sebio A, Salazar J, Berenguer-Llergo A, Río E, Barnadas A, Baiget M, Páez |
Genetic variants associated with colorectal brain metastases susceptibility and survival. The pharmacogenomics journal 2015 Dec . Stremitzer S, Berghoff A S, Volz N B, Zhang W, Yang D, Stintzing S, Ning Y, Sunakawa Y, Yamauchi S, Sebio A, Matsusaka S, Okazaki S, Hanna D, Parekh A, Mendez A, Berger M D, El-Khoueiry R, Birner P, Preusser M, Lenz H |
Genetic variants in the ITGB6 gene is associated with the risk of radiation pneumonitis in lung cancer patients treated with thoracic radiation therapy. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Oct . Yi Minxiao, Tang Yang, Liu Bo, Li Qianxia, Zhou Xiao, Yu Shiying, Fu Shengling, Cai Yixin, Yuan Xiangl |
Integrins AV and B8 Gene Polymorphisms and Risk for Intracerebral Hemorrhage in Greek and Polish Populations. Neuromolecular medicine 2016 Jul . Dardiotis Efthimios, Siokas Vasileios, Zafeiridis Tilemachos, Paterakis Konstantinos, Tsivgoulis Georgios, Dardioti Maria, Grigoriadis Savas, Simeonidou Constantina, Deretzi Georgia, Zintzaras Elias, Jagiella Jeremiasz, Hadjigeorgiou Georgios |
Distinct Subtypes of Gastric Cancer Defined by Molecular Characterization Include Novel Mutational Signatures with Prognostic Capability. Cancer research 2016 04 76 (7): 1724-32. Li Xiangchun, Wu William K K, Xing Rui, Wong Sunny H, Liu Yuexin, Fang Xiaodong, Zhang Yanlin, Wang Mengyao, Wang Jiaqian, Li Lin, Zhou Yong, Tang Senwei, Peng Shaoliang, Qiu Kunlong, Chen Longyun, Chen Kexin, Yang Huanming, Zhang Wei, Chan Matthew T V, Lu Youyong, Sung Joseph J Y, Yu J |
Lack of association between integrin aß gene polymorphisms and hemorrhagic fever with renal syndrome in Han Chinese from Hubei, China. Virologica Sinica 2017 Feb . Chen Xiao-Ping, Xiong Hai-Rong, Zhu Ni, Chen Qing-Zhou, Wang Hui, Zhong Chao-Jie, Wang Mei-Rong, Lu Shuang, Luo Fan, Hou W |
Genetic variants in the VEGF pathway as prognostic factors in stages II and III colon cancer. The pharmacogenomics journal 2017 Dec . Riera Pau, Virgili Anna C, Salazar Juliana, Sebio Ana, Tobeña María, Sullivan Ivana, Páez Dav |
"Omics" data integration and functional analyses link Enoyl-CoA hydratase, short chain 1 to drug refractory dilated cardiomyopathy. BMC medical genomics 2018 12 11 (1): 110. Campbell Nzali V, Weitzenkamp David A, Campbell Ian L, Schmidt Ronald F, Hicks Chindo, Morgan Michael J, Irwin David C, Tentler John |
Voltage-gated calcium channel activity and complex related genes and schizophrenia: A systematic investigation based on Han Chinese population. Journal of psychiatric research 2018 10 106 99-105. Zhang Tianxiao, Zhu Li, Ni Tong, Liu Dan, Chen Gang, Yan Zhilan, Lin Huali, Guan Fanglin, Rice John |
Effect of integrin AV and B8 gene polymorphisms in patients with traumatic brain injury. Brain injury 2019 Apr 1-10. Dardiotis Efthimios, Siokas Vasileios, Aloizou Athina-Maria, Karampinis Emmanouil, Brotis Alexandros G, Grigoriadis Savas, Paterakis Konstantinos, Dardioti Maria, Komnos Apostolos, Kapsalaki Eftychia, Fountas Kostas, Hadjigeorgiou Georgios |
Prognostic effect of VEGF gene variants in metastatic non-small-cell lung cancer patients. Angiogenesis 2019 Apr . Sullivan Ivana, Riera Pau, Andrés Marta, Altés Albert, Majem Margarita, Blanco Remei, Capdevila Laia, Barba Andrés, Barnadas Agustí, Salazar Julia |
Exploring Single Nucleotide Polymorphisms in ITGAV for Gastric, Pancreatic and Liver Malignancies: An Approach Towards the Discovery of Biomarker. Combinatorial chemistry & high throughput screening 2020 8 24 (6): 860-873. Bhattacharya Shreya, Sah Pragati Prasad, Banerjee Arundhati, Ray Suj |
Association of ITGAV polymorphisms and risk of rheumatoid arthritis: evidence from a meta-analysis. Expert review of clinical immunology 2020 Jun . Huang Jun-Ming, Pang Zhi-Ying, Qi Guo-Bin, Wang Zhe, Lv Zheng-T |
Unique molecular features and clinical outcomes in young patients with non-small cell lung cancer harboring ALK fusion genes. Journal of cancer research and clinical oncology 2020 Jan . Tian Panwen, Liu Yujie, Zeng Hao, Tang Yuan, Lizaso Analyn, Ye Junyi, Shao Lin, Li Yal |
Rs868058 in the Homeobox Gene HLX Contributes to Early-Onset Fetal Growth Restriction. Biology 2022 3 11 (3): . Wujcicka Wioletta Izabela, Kacerovsky Marian, Krekora Micha?, Kaczmarek Piotr, Le?niczak Beata, Grzesiak Mariu |
Whole-genome resequencing reveals new mutations in candidate genes for Beichuan-white goat prolificacya. Animal biotechnology 2023 9 1-12. Aimin Zhou, Yi Ding, Xiaohui Zhang, Yugang Zhou, Yadong Liu, Tingjian Li, Long Xi |
Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study. Brain & spine 2023 6 3 101745. Markus K H Wiedmann, Ingunn V Steinsvåg, Tovy Dinh, Magnus D Vigeland, Pål G Larsson, Hanne Hjorthaug, Ying Sheng, Inger-Lise Mero, Kaja K Selm |
An Integrated Computational Analysis of High-Risk SNPs in Angiopoietin-like Proteins (ANGPTL3 and ANGPTL8) Reveals Perturbed Protein Dynamics Associated with Cancer. Molecules (Basel, Switzerland) 2023 6 28 (12): . Sajid Iqbal, Farida Begum, Dorothy Wavinya Nyamai, Nasir Jalal, Peter Sh |
Whole-exome sequencing in searching for novel variants associated with the development of high altitude pulmonary edema. Gene 2023 3 870 147384. Chen Mingyue, Yi Faling, Qi Yijin, Zhao Beibei, Zhang Zhanhao, He Xue, Yuan Dongya, Jin Tian |
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- Page last updated:Apr 22, 2024
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