Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: IQGAP1[original query] |
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Genetic variants at the miR-124 binding site on the cytoskeleton-organizing IQGAP1 gene confer differential predisposition to breast cancer. International journal of oncology 2011 Apr 38 (4): 1153-61. Zheng Hong, Song Fengju, Zhang Lina, Yang Da, Ji Ping, Wang Yingmei, Almeida Maria, Calin George A, Hao Xishan, Wei Qingyi, Zhang Wei, Chen Kex |
A functional MiR-124 binding-site polymorphism in IQGAP1 affects human cognitive performance. PloS one 2014 9 (9): e107065. Yang Lixin, Zhang Rui, Li Ming, Wu Xujun, Wang Jianhong, Huang Lin, Shi Xiaodong, Li Qingwei, Su Bi |
Allelic imbalance of multiple sclerosis susceptibility genes IKZF3 and IQGAP1 in human peripheral blood. BMC genetics 2016 17 (1): 59. Keshari Pankaj K, Harbo Hanne F, Myhr Kjell-Morten, Aarseth Jan H, Bos Steffan D, Berge To |
Identification of new susceptibility loci associated with rheumatoid arthritis.
Annals of the rheumatic diseases 2020 Aug . Leng Rui-Xue, Di Dong-Sheng, Ni Jing, Wu Xiao-Xiao, Zhang Lin-Lin, Wang Xu-Fan, Liu Rui-Shan, Huang Qian, Fan Yin-Guang, Pan Hai-Feng, Wang Bin, Ye Dong-Qi |
Exome sequencing in patients with microphthalmia, anophthalmia, and coloboma (MAC) from a consanguineous population. Clinical genetics 2020 8 98 (5): 499-506. Islam Farrah, Htun Stephanie, Lai Li-Wen, Krall Max, Poranki Menitha, Martin Pierre-Marie, Sobreira Nara, Wohler Elizabeth S, Yu Jingwei, Moore Anthony T, Slavotinek Anne |
Genetic Variability in the microRNA Binding Sites of BMPR1B, TGFBR1, IQGAP1, KRAS, SETD8 and RYR3 and Risk of Breast Cancer in Colombian Women. OncoTargets and therapy 2020 13 12281-12287. Garcia Mesa Karen, Bermejo Justo Lorenzo, Torres Diana, Gilbert Michael, Plass Christoph, Hamann U |
The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study.
Anaesthesia 2020 01 75 Suppl 1 e111-e120. van Reij R R I, Hoofwijk D M N, Rutten B P F, Weinhold L, Leber M, Joosten E A J, Ramirez A, van den Hoogen N J, |
De novo variants in exomes of congenital heart disease patients identify risk genes and pathways. Genome medicine 2020 1 12 (1): 9. Sevim Bayrak Cigdem, Zhang Peng, Tristani-Firouzi Martin, Gelb Bruce D, Itan Yuv |
RASGRF1 Fusions Activate Oncogenic RAS Signaling and Confer Sensitivity to MEK Inhibition. Clinical cancer research : an official journal of the American Association for Cancer Research 2022 3 28 (14): 3091-3103. Hunihan Lisa, Zhao Dejian, Lazowski Heather, Li Man, Qian Yuping, Abriola Laura, Surovtseva Yulia V, Muthusamy Viswanathan, Tanoue Lynn T, Rothberg Bonnie E Gould, Schalper Kurt A, Herbst Roy S, Wilson Frederick |
Exome sequencing findings in children with annular pancreas. Molecular genetics & genomic medicine 2023 8 e2233. Georgia Pitsava, Nathan Pankratz, John Lane, Wei Yang, Shannon Rigler, Gary M Shaw, James L Mil |
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- Page last updated:Apr 22, 2024
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