Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 34 Records) |
Query Trace: NFATC1[original query] |
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Absence of association between length variation of an intronic region in the NFATC1 gene and congenital heart defects in a Han Chinese population. DNA and cell biology 2012 Jan 31 (1): 88-91. Liu Hanmin, Dai Li, Mao Meng, Wang Xiaoshuang, Hua Yimin, Xie Lia |
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 |
Association of Genes Variants in RANKL/RANK/OPG Signaling Pathway with the Development of Osteonecrosis of the Femoral Head in Chinese Population. International journal of medical sciences 2017 14 (7): 690-697. Song Yang, Du Zhen-Wu, Yang Qi-Wei, Ren Ming, Wang Qing-Yu, Wang Ao, Chen Gao-Yang, Zhao Hai-Yue, Yu Tao, Zhang Gui-Zh |
NFATC1 genotypes affect acute rejection and long-term graft function in cyclosporine-treated renal transplant recipients. Pharmacogenomics 2017 Mar 18 (4): 381-392. Xu Qinxia, Qiu Xiaoyan, Jiao Zheng, Zhang Ming, Chen Jianping, Zhong Mingka |
CRELD1 gene variants and atrioventricular septal defects in Down syndrome. Gene 2017 10 641 180-185. Asim Ambreen, Agarwal Sarita, Panigrahi Inusha, Sarangi Aditya Narayan, Muthuswamy Srinivasan, Kapoor Adit |
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 |
Identification of potential regulatory mutations using multi-omics analysis and haplotyping of lung adenocarcinoma cell lines. Scientific reports 2018 3 8 (1): 4926. Sereewattanawoot Sarun, Suzuki Ayako, Seki Masahide, Sakamoto Yoshitaka, Kohno Takashi, Sugano Sumio, Tsuchihara Katsuya, Suzuki Yuta |
The stiffness response of type IIa fibres after eccentric exercise-induced muscle damage is dependent on ACTN3 r577X polymorphism. European journal of sport science 2018 10 19 (4): 480-489. Broos Siacia, Malisoux Laurent, Theisen Daniel, Van Thienen Ruud, Francaux Marc, Thomis Martine A, Deldicque Loui |
Genetic Variants at the rs4720169 Locus of TBX20 and the rs12921862 Locus of AXIN1 May Increase the Risk of Congenital Heart Defects in the Mexican Population: A Pilot Study. Genetic testing and molecular biomarkers 2019 9 23 (9): 664-670. Hernández-Almaguer Maria Dolores, Calvo-Anguiano Geovana, Cerda-Flores Ricardo M, Salinas-Torres Víctor M, Orozco-Galicia Francisco, Glenn Eva, García-Guerra Jaime, Sánchez-Cortés Gerardo, Lugo-Trampe José, Martínez-Garza Laura |
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 |
Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry.
Frontiers in genetics 2018 9 659. Rolfe Sara, Lee Su-In, Shapiro Lin |
Functional fine-mapping of noncoding risk variants in amyotrophic lateral sclerosis utilizing convolutional neural network. Scientific reports 2020 8 10 (1): 12872. Yousefian-Jazi Ali, Sung Min Kyung, Lee Taeyeop, Hong Yoon-Ho, Choi Jung Kyoon, Choi Jinwo |
An intronic polymorphism of NFATC1 gene shows a risk association with biopsy-proven acute rejection in renal transplant recipients. Annals of translational medicine 2020 Mar 8 (5): 211. Wang Zijie, Zhang Hengcheng, Yang Haiwei, Zheng Ming, Guo Miao, Chen Hao, Sun Li, Han Zhijian, Tao Jun, Ju Xiaobing, Tan Ruoyun, Wei Ji-Fu, Gu M |
FKBP-CaN-NFAT pathway polymorphisms selected by in silico biological function prediction are associated with tacrolimus efficacy in renal transplant patients. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 2020 Dec 105694. Zheng Xinyi, Huai Cong, Xu Qinxia, Xu Luyang, Zhang Ming, Zhong Mingkang, Qiu Xiaoy |
Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia. Blood 2020 11 137 (20): 2800-2816. Klintman Jenny, Appleby Niamh, Stamatopoulos Basile, Ridout Katie, Eyre Toby A, Robbe Pauline, Pascua Laura Lopez, Knight Samantha J L, Dreau Helene, Cabes Maite, Popitsch Niko, Ehinger Mats, Martín-Subero Jose I, Campo Elías, Månsson Robert, Rossi Davide, Taylor Jenny C, Vavoulis Dimitrios V, Schuh An |
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 |
Estrogen receptor alpha and NFATc1 bind to a bone mineral density-associated SNP to repress WNT5B in osteoblasts. American journal of human genetics 2021 12 109 (1): 97-115. Suthon Sarocha, Lin Jianjian, Perkins Rachel S, Crockarell John R, Miranda-Carboni Gustavo A, Krum Susan |
Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population. Italian journal of pediatrics 2022 7 48 (1): 124. Sarwar Sumbal, Shabana , Tahir Amna, Liaqat Zainab, Naseer Saher, Seme Rani Summeya, Mehmood Sabahat, Shahid Saleem Ullah, Hasnain Shahi |
Association between SEMA3A signaling pathway genes and BMD/OP risk: An epidemiological and experimental study. Frontiers in endocrinology 2022 11 13 1014431. Zhou Hao-Long, Wei Mu-Hong, Di Dong-Sheng, Zhang Ru-Yi, Zhang Jian-Li, Yuan Ting-Ting, Liu Qian, Zhou Ting-Ting, Huang Qin, Wang |
Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans. HGG advances 2022 Jan 3 (1): 100082. Null Megan, Yilmaz Feyza, Astling David, Yu Hung-Chun, Cole Joanne B, Hallgrímsson Benedikt, Santorico Stephanie A, Spritz Richard A, Shaikh Tamim H, Hendricks Audrey |
Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing. Genomics 2023 7 115 (5): 110676. JiaJun Ye, Yiwei Niu, Yongxuan Peng, Jihong Huang, Huiying Wang, Qihua Fu, Fen Li, Rang Xu, Sun Chen, Yuejuan Xu, Kun S |
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 |
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- Page last updated:Apr 16, 2024
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