Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: ITGB4[original query] |
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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 |
Association of polymorphisms in microRNA-binding sites and colorectal cancer in an Iranian population. Cancer genetics 2012 Oct 205 (10): 501-7. Azimzadeh Pedram, Romani Sara, Mohebbi Seyed Reza, Mahmoudi Touraj, Vahedi Mohsen, Fatemi Seyed Reza, Zali Narges, Zali Mohammad Re |
Association between polymorphisms of microRNA-binding sites in integrin genes and gastric cancer in Chinese Han population. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Apr 36 (4): 2785-92. Song Xingbo, Zhong Huiyu, Zhou Juan, Hu Xuejiao, Zhou Yi, Ye Yuanxin, Lu Xiaojun, Wang Jun, Ying Binwu, Wang Lanl |
Elevated integrin a6ß4 expression is associated with venous invasion and decreased overall survival in non-small cell lung cancer. Human pathology 2016 Apr . Stewart Rachel L, West Dava, Wang Chi, Weiss Heidi L, Gal Tamas, Durbin Eric, O'Connor William, Chen Min, O'Connor Kathleen |
Rare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITG?4 gene in schizophrenia and bipolar disorder. Schizophrenia research 2018 Mar . O'Brien N L, Fiorentino A, Curtis D, Rayner C, Petrosellini C, Al Eissa M, Bass N J, McQuillin A, Sharp S |
[Somatic Mutations Associated with Metastasis in Acral Melanoma]. Molekuliarnaia biologiia 2019 8 53 (4): 648-653. Abramov I S, Emelyanova M A, Ryabaya O O, Krasnov G S, Zasedatelev A S, Nasedkina T |
A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome. Annals of clinical and laboratory science 2019 7 49 (3): 330-337. Li Yongzhen, He Qingnan, Wang Ying, Dang Xiqiang, Wu Xiaochuan, Li Xiaoyan, Shuai Lanjun, Yi Zhuw |
Common variants of NRG1 and ITGB4 confer risk of Hirschsprung disease in Han Chinese population. Journal of pediatric surgery 2020 Apr . Wei Zhiliang, Yu Xianxian, Wu Wenjie, Bai Meirong, Lu Yanjiao, Song Huanlei, Gong Yiming, Gu Beilin, Chu Xun, Cai W |
Whole Exome Sequencing Identifies Two Novel Mutations in a Patient with UC Associated with PSC and SSA. Canadian journal of gastroenterology & hepatology 2021 9 2021 9936932. Wu Dong, Chen Dan, Shi Wen, Liu Wei, Zhou Weixun, Qian Jiami |
Whole-Exome Sequencing Reveals Rare Germline Mutations in Patients With Hemifacial Microsomia. Frontiers in genetics 2021 6 12 580761. Chen Xiaojun, Liu Fatao, Mar Aung Zin, Zhang Yan, Chai Ga |
Epidermolysis Bullosa in Chinese Patients: Genetic Analysis and Mutation Landscape in 57 Pedigrees and Sporadic Cases. Acta dermato-venereologica 2021 5 101 (7): adv00503. Yu Yueqian, Wang Zhenzhen, Mi Zihao, Sun Lele, Fu Xi'an, Yu Gongqi, Pang Zheng, Liu Hong, Zhang Fur |
Novel pathogenic variants in an Indian cohort with epidermolysis bullosa: Expanding the genotypic spectrum. European journal of medical genetics 2021 10 64 (12): 104345. Nilay Mayank, Saxena Deepti, Mandal Kausik, Moirangthem Amita, Phadke Shubha |
Tacrolimus in the treatment of childhood nephrotic syndrome: Machine learning detects novel biomarkers and predicts efficacy. Pharmacotherapy 2022 12 43 (1): 43-52. Mo Xiaolan, Chen Xiujuan, Zeng Huasong, Zheng Wei, Ieong Chifong, Li Huixian, Huang Qiongbo, Xu Zichuan, Yang Jinlian, Liang Qianying, Liang Huiying, Gao Xia, Huang Min, Li Jia |
Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population. Kidney international 2023 12 . Precil D Neves, Andreia Watanabe, Elieser H Watanabe, Amanda M Narcizo, Kelly Nunes, Antonio M Lerario, Frederico Moraes Ferreira, Lívia B Cavalcante, Janewit Wongboonsin, Denise M Malheiros, Lectícia B Jorge, Matthew G Sampsom, Irene L Noronha, Luiz F Onuch |
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- Page last updated:Mar 18, 2024
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