Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 34 Records) |
Query Trace: THBS1[original query] |
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Polymorphisms associated with in vitro aspirin resistance are not associated with clinical outcomes in patients with coronary artery disease who report regular aspirin use. American heart journal 2011 Jul 162 (1): 166-72.e1. Voora Deepak, Horton John, Shah Svati H, Shaw Linda K, Newby L Krist |
Polymorphism of THBS1 rs1478604 A>G in 5-untranslated region is associated with lymph node metastasis of gastric cancer in a Southeast Chinese population. DNA and cell biology 2012 Apr 31 (4): 511-9. Lin Xian-Dong, Chen Shu-Qin, Qi Yuan-Lin, Zhu Jin-Wei, Tang Yang, Lin Jian-Y |
Association between variations in coagulation system genes and carotid plaque. Journal of the neurological sciences 2012 Dec 323 (1-2): 93-8. Della-Morte David, Beecham Ashley, Dong Chuanhui, Wang Liyong, McClendon Mark S, Gardener Hannah, Blanton Susan H, Sacco Ralph L, Rundek Tatja |
Association of thrombospondin 1 gene with schizophrenia in Korean population. Molecular biology reports 2012 Jun 39 (6): 6875-80. Park Hae Jeong, Kim Su Kang, Kim Jong Woo, Kang Won Sub, Chung Joo- |
Polymorphism in THBS1 gene is associated with post-refractive surgery chronic ocular surface inflammation. Ophthalmology 2014 Jul 121 (7): 1389-97. Contreras-Ruiz Laura, Ryan Denise S, Sia Rose K, Bower Kraig S, Dartt Darlene A, Masli Sharmi |
Common and rare variants of the THBS1 gene associated with the risk for autism. Psychiatric genetics 2014 Dec 24 (6): 235-40. Lu Lina, Guo Hui, Peng Yu, Xun Guanglei, Liu Yanling, Xiong Zhimin, Tian Di, Liu Yalan, Li Wei, Xu Xiaojuan, Zhao Jingping, Hu Zhengmao, Xia K |
Polymorphisms in host genes encoding NOSII, C-reactive protein, and adhesion molecules thrombospondin and E-selectin are risk factors for Plasmodium falciparum malaria in India. European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology 2015 Oct 34 (10): 2029-39. Kanchan K, Pati S S, Mohanty S, Mishra S K, Sharma S K, Awasthi S, , Venkatesh V, Habib |
Association of THBS1 rs1478605 T>C in 5'-untranslated regions with the development and progression of gastric cancer. Biomedical reports 2015 Mar 3 (2): 207-214. Hong Bin-Bin, Chen Shu-Qin, Qi Yuan-Lin, Zhu Jin-Wei, Lin Jian-Y |
Association between single nucleotide polymorphisms in thrombospondins genes and coronary artery disease: A meta-analysis. Thrombosis research 2015 Jul 136 (1): 45-51. Zhang Xiao-Jie, Wei Chun-Yan, Li Wen-Bo, Zhang Ling-Li, Zhou Ying, Wang Zhi-Hao, Tang Meng-Xiong, Zhang Wei, Zhang Yun, Zhong Mi |
Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts. Human genetics 2015 Nov . Conte Federica, Oti Martin, Dixon Jill, Carels Carine E L, Rubini Michele, Zhou Huiqi |
Genome-wide copy number analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer. Urologic oncology 2017 09 35 (9): 545.e1-545.e11. Poniah Prevathe, Mohd Zain Shamsul, Abdul Razack Azad Hassan, Kuppusamy Shanggar, Karuppayah Shankar, Sian Eng Hooi, Mohamed Zahur |
Tobacco habituated and non-habituated subjects exhibit different mutational spectrums in head and neck squamous cell carcinoma. 3 Biotech 2017 3 5 (5): 685-696. Rawal Rakesh M, Joshi Madhvi N, Bhargava Poonam, Shaikh Inayat, Pandit Aanal S, Patel Riddhi P, Patel Shanaya, Kothari Kiran, Shah Manoj, Saxena Akshay, Bagatharia Snehal |
Spectrum of germline mutations in smokers and non-smokers in Brazilian non-small-cell lung cancer (NSCLC) patients. Carcinogenesis 2017 Aug . Couto Patrícia P, Bastos-Rodrigues Luciana, Schayek Hagit, Melo Flavia M, Lisboa Raony G C, Miranda Debora M, Vilhena Alyne, Bale Allen E, Friedman Eitan, De Marco Lu |
Targeted next-generation sequencing identifies clinically relevant somatic mutations in a large cohort of inflammatory breast cancer. Breast cancer research : BCR 2018 Aug 20 (1): 88. Liang Xu, Vacher Sophie, Boulai Anais, Bernard Virginie, Baulande Sylvain, Bohec Mylene, Bièche Ivan, Lerebours Florence, Callens Céli |
Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy.
Annals of neurology 2018 Jul . Weiss Robert B, Vieland Veronica J, Dunn Diane M, Kaminoh Yuuki, Flanigan Kevin M, |
The Role of Polymorphic Markers rs1478604, rs2292305, and rs2228262 in THBS1 Gene in the Development of Autoimmune Dry Eye Syndrome. Bulletin of experimental biology and medicine 2020 9 169 (5): 707-709. Safonova T N, Surnina Z V, Zaitseva G V, Burdennyi A M, Loginov V |
Evaluation of thrombospondin-1 gene polymorphisms in corneal allograft rejection in Asian Indian patients. Indian journal of ophthalmology 2020 3 68 (4): 565-572. Vanathi Murugesan, Shukla Rashmi, Balakrishnan Prahlad, Dwivedi Roopa, Gupta Noopur, Tandon Radhi |
Progressive and Prognostic Performance of an Extracellular Matrix-Receptor Interaction Signature in Gastric Cancer. Disease markers 2020 2020 8816070. Yang Xiangchou, Chen Liping, Mao Yuting, Hu Zijing, He Muqi |
Identification of New Therapeutic Targets for Gastric Cancer With Bioinformatics. Frontiers in genetics 2020 10 11 865. Li Yang, Wang Jin-Shen, Zhang Tao, Wang Hong-Chang, Li Le-Pi |
Hypertensive Patients Exhibit Enhanced Thrombospondin-1 Levels at High-Altitude. Life (Basel, Switzerland) 2021 9 11 (9): . Sharma Kavita, Chanana Neha, Mohammad Ghulam, Thinlas Tashi, Gupta Mohit, Syed Mansoor Ali, Das Rajat Subhra, Pasha Qadar, Mishra Aast |
Genetic Modifiers and Phenotype of Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis. Pharmaceuticals (Basel, Switzerland) 2021 8 14 (8): . Pascual-Morena Carlos, Cavero-Redondo Iván, Saz-Lara Alicia, Sequí-Domínguez Irene, Lucerón-Lucas-Torres Maribel, Martínez-Vizcaíno Vicen |
Diagnostic, Therapeutic, and Prognostic Value of the Thrombospondin Family in Gastric Cancer. Frontiers in molecular biosciences 2021 5 8 647095. Lu Yi, Kong Xianhe, Zhong Weijie, Hu Minhui, Li Chuj |
Thrombospondin 1 polymorphism associated with decreased expression and increased risk of pterygium. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2021 Mar . Simon Lilla S, Keshav Vinny, Baharozian Connor, Masli Sharmila, Lee Hyunjoo |
The Integrative Analysis of Thrombospondin Family Genes in Pan-Cancer Reveals that THBS2 Facilitates Gastrointestinal Cancer Metastasis. Journal of oncology 2021 11 2021 4405491. Zhang Chunfeng, Hu Chenyu, Su Kunqi, Wang Kun, Du Xiaojuan, Xing Baocai, Liu Xiaofe |
The genetic architecture of language functional connectivity.
NeuroImage 2021 12 249 118795. Mekki Yasmina, Guillemot Vincent, Lemaître Hervé, Carrión-Castillo Amaia, Forkel Stephanie, Frouin Vincent, Philippe Cat |
Genetic regulation of THBS1 methylation in diabetic retinopathy. Frontiers in endocrinology 2022 12 13 991803. Li Yaqi, Gong Chunmei, Xu Yuanfei, Liang Xiongshun, Chen Xiaoping, Hong Wenxu, Yan Junx |
Evaluating Genetic Modifiers of Duchenne Muscular Dystrophy Disease Progression Using Modeling and MRI. Neurology 2022 10 99 (21): e2406-e2416. Barnard Alison M, Hammers David W, Triplett William T, Kim Sarah, Forbes Sean C, Willcocks Rebecca J, Daniels Michael J, Senesac Claudia R, Lott Donovan J, Arpan Ishu, Rooney William D, Wang Richard T, Nelson Stanley F, Sweeney H Lee, Vandenborne Krista, Walter Glenn |
Association of THBS1 genetic variants and mRNA expression with the risks of ischemic stroke and long-term death after stroke. Frontiers in aging neuroscience 2022 14 1006473. Chen Changying, Chen Xuemei, Yang Siyuan, Li Qingqing, Ren Zhanyun, Wang Lu, Jiang Yuzhang, Gu Xincheng, Liu Fangyuan, Mu Jialing, Liu Lihua, Wang Yi, Li Junrong, Yu Yanhua, Zhang Jun, Shen Cho |
A-296G variant of THBS1 gene (rs1478605) is associated with a lower frequency of stroke in a Brazilian population with sickle cell anemia. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2023 11 33 (1): 107474. Jessica M F Oliveira, Gabriela S Arcanjo, Igor F Domingos, Jéssica V G F Batista, Diego A Pereira-Martins, Thais H C Batista, Betânia L D Hatzlhofer, Diego A Falcão, Madi V Diniz, Alexsandro P Silva, Bárbara C V Pires, Ana C Dos Anjos, Fernando F Costa, Aderson S Araujo, Antonio R Lucena-Araujo, Marcos A Bezer |
[Predictive significance of genetic analysis of the development of dry eye disease of different origin]. Vestnik oftalmologii 2024 1 139 (6): 13-18. T N Safonova, G V Zaitseva, V I Loginov, A M Burdenn |
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- Page last updated:Apr 16, 2024
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