Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: ITGB8[original query] |
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Genome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinoma. BMC medical genomics 2008 Jun 1 (1): 25. Blons H, Pallier K, Le Corre D, Danel C, Tremblay M, Houdayer C, Fabre-Guillevin E, Riquet M, Dessen P, Laurent-Puig P |
Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries. International journal of cardiology 2015 Nov 204 115-121. Costain Gregory, Lionel Anath C, Ogura Lucas, Marshall Christian R, Scherer Stephen W, Silversides Candice K, Bassett Anne |
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 |
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
Nature genetics 2017 Jan . de Lange Katrina M, Moutsianas Loukas, Lee James C, Lamb Christopher A, Luo Yang, Kennedy Nicholas A, Jostins Luke, Rice Daniel L, Gutierrez-Achury Javier, Ji Sun-Gou, Heap Graham, Nimmo Elaine R, Edwards Cathryn, Henderson Paul, Mowat Craig, Sanderson Jeremy, Satsangi Jack, Simmons Alison, Wilson David C, Tremelling Mark, Hart Ailsa, Mathew Christopher G, Newman William G, Parkes Miles, Lees Charlie W, Uhlig Holm, Hawkey Chris, Prescott Natalie J, Ahmad Tariq, Mansfield John C, Anderson Carl A, Barrett Jeffrey |
Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia. Molecular genetics & genomic medicine 2018 May 6 (3): 350-356. Pawlikowska Ludmila, Nelson Jeffrey, Guo Diana E, McCulloch Charles E, Lawton Michael T, Kim Helen, Faughnan Marie E, |
Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population.
Biomedical reports 2018 Nov 9 (5): 383-404. Yamada Yoshiji, Yasukochi Yoshiki, Kato Kimihiko, Oguri Mitsutoshi, Horibe Hideki, Fujimaki Tetsuo, Takeuchi Ichiro, Sakuma J |
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 |
Coexisting EGFR and TP53 Mutations in Lung Adenocarcinoma Patients Are Associated With COMP and ITGB8 Upregulation and Poor Prognosis. Frontiers in molecular biosciences 2020 3 7 30. Zheng Chang, Li Xuelian, Ren Yangwu, Yin Zhihua, Zhou Baos |
Eight novel susceptibility loci and putative causal variants in atopic dermatitis.
The Journal of allergy and clinical immunology 2021 Jun . Tanaka Nao, Koido Masaru, Suzuki Akari, Otomo Nao, Suetsugu Hiroyuki, Kochi Yuta, Tomizuka Kouhei, Momozawa Yukihide, Kamatani Yoichiro, , Ikegawa Shiro, Yamamoto Kazuhiko, Terao Chikas |
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- Page last updated:Apr 22, 2024
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