Human Genome Epidemiology Literature Finder
|
Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and ITGAV[original query] |
|---|
| 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 |
| 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 |
| 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 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 |
| 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 |
| "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 |
| 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 |
| 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-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 |
| 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 |
- Page last reviewed:Feb 1, 2024
- Content source: