Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Disease and NFATC1[original query] |
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| Differential duplication of an intronic region in the NFATC1 gene in patients with congenital heart disease. Genome / National Research Council Canada = Génome / Conseil national de recherches Canada 2006 Sep 49 (9): 1092-8. Yehya Amin, Souki Ramzi, Bitar Fadi, Nemer Georg |
| [Association between nuclear factor of activated T cells 1 gene mutation and simple congenital heart disease in children]. Zhonghua xin xue guan bing za zhi 2010 Jul 38 (7): 621-4. Han Zeng-qiang, Chen Yu, Tang Chu-zhong, Gao Wen-gen, Xie Ji-yan, Hu Da- |
| Association of a tandem repeat polymorphism in NFATc1 with increased risk of perimembranous ventricular septal defect in a Chinese population. Biochemical genetics 2011 Oct 49 (9-10): 592-600. Gu Haiyong, Gong Jie, Qiu Wanshan, Cao Hailong, Xu Jing, Chen Suocheng, Chen Yijia |
| High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease. American journal of medical genetics. Part A 2013 Dec 161A (12): 3087-94. Zhao Wei, Niu Guannan, Shen Botao, Zheng Yang, Gong Fangchao, Wang Xianfu, Lee Jiyun, Mulvihill John J, Chen Xiaohui, Li Shi |
| Association of NFATc1 gene polymorphism with ventricular septal defect in the Chinese Han population. Chinese medical journal 2013 Jan 126 (1): 1. Shen L, Li ZZ, Shen AD, Liu H, Bai S, Guo J, Yuan F, Li XF |
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity.
American journal of human genetics 2016 Sep 99 (3): 636-46. Mahajan Anubha, Rodan Aylin R, Le Thu H, Gaulton Kyle J, Haessler Jeffrey, Stilp Adrienne M, Kamatani Yoichiro, Zhu Gu, Sofer Tamar, Puri Sanjana, Schellinger Jeffrey N, Chu Pei-Lun, Cechova Sylvia, van Zuydam Natalie, , , Arnlov Johan, Flessner Michael F, Giedraitis Vilmantas, Heath Andrew C, Kubo Michiaki, Larsson Anders, Lindgren Cecilia M, Madden Pamela A F, Montgomery Grant W, Papanicolaou George J, Reiner Alex P, Sundström Johan, Thornton Timothy A, Lind Lars, Ingelsson Erik, Cai Jianwen, Martin Nicholas G, Kooperberg Charles, Matsuda Koichi, Whitfield John B, Okada Yukinori, Laurie Cathy C, Morris Andrew P, Franceschini No |
| Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population. Pediatric cardiology 2016 Dec 37 (8): 1548-1561. Wang Fengyu, Wang Haili, Wang Lina, Zhou Shiyuan, Chang Mingxiu, Zhou Jiping, Dou Yongheng, Wang Yanli, Shi Xiangdo |
| From Genetic Predisposition to Molecular Mechanisms of Autoimmune Primary Adrenal Insufficiency. Frontiers of hormone research 2016 46 115-32. Falorni Alberto, Brozzetti Annalisa, Perniola Rober |
| Correlation between NFATC1 gene polymorphisms and congenital heart disease in children. European review for medical and pharmacological sciences 2017 Aug 21 (15): 3441-3446. Li C-L, Niu L, Fu M-Y, Tian J, Wang Q-W, An X |
| Meta-Analysis of Genome-Wide Association Studies Identifies Novel Functional CpG-SNPs Associated with Bone Mineral Density at Lumbar Spine. International journal of genomics 2018 2018 6407257. Qiu Chuan, Shen Hui, Fu Xiaoying, Xu Chao, Deng Hongw |
| Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients. PloS one 2018 13 (6): e0199003. Lanata Cristina M, Nititham Joanne, Taylor Kimberly E, Chung Sharon A, Torgerson Dara G, Seldin Michael F, Pons-Estel Bernardo A, Tusié-Luna Teresa, Tsao Betty P, Morand Eric F, Alarcón-Riquelme Marta E, Criswell Lindsey |
| Association of Variant Interactions in RANK, RANKL, OPG, TRAF6, and NFATC1 Genes with the Development of Osteonecrosis of the Femoral Head. DNA and cell biology 2019 May . Chen Bingpeng, Du Zhenwu, Dong Xiaoming, Li Zhaoyan, Wang Qingyu, Chen Gaoyang, Zhang Guizhen, Song Ya |
| Altered expression of nuclear factor of activated T cells, forkhead box P3, and immune-suppressive genes in regulatory T cells of generalized vitiligo patients. Pigment cell & melanoma research 2020 Jan . Giri Prashant S, Dwivedi Mitesh, Laddha Naresh C, Begum Rasheedunnisa, Bharti Ankit |
| Genetic association of nuclear factor of activated T cells' 3'UTR and structural polymorphisms with susceptibility to generalized vitiligo in Gujarat population. Gene 2023 7 880 147629. Prashant Giri, Radhika Bhimani, Siddhika Patil, Mitesh Dwive |
| Genetic studies in the Pakistani population reveal novel associations with ventricular septal defects (VSDs). BMC pediatrics 2023 2 23 (1): 67. Sarwar Sumbal, Shabana , Sajjad Khadija, Hasnain Shahi |
| Risk Variants in or Near ZBTB40 AND NFATC1 Increase the Risk of Both IBD and Adverse Bone Health Outcomes Highlighting Common Genetic Underpinnings Across Both Diseases. Inflammatory bowel diseases 2023 1 . Cushing Kelly C, Chen Yanhua, Du Xiaomeng, Chen Vincent, Kuppa Annapurna, Higgins Peter, Speliotes Elizabeth |
- Page last reviewed:Feb 1, 2024
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