Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and KLK1[original query] |
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| Association of the tissue kallikrein gene promoter with ESRD and hypertension. Kidney international 2002 Mar 61 (3): 1030-9. Yu Hongrun, Song Qing, Freedman Barry I, Chao Julie, Chao Lee, Rich Stephen S, Bowden Donald |
| Significance of the tissue kallikrein promoter and transforming growth factor-beta1 polymorphisms with renal progression in children with vesicoureteral reflux. Kidney international 2004 Apr 65 (4): 1467-72. Lee-Chen GJ, Liu KP, Lai YC, Juang HS, Huang SY, Lin CY |
| Apolipoprotein E, angiotensin-converting enzyme and kallikrein gene polymorphisms and the risk of Alzheimer's disease and vascular dementia. Journal of neural transmission (Vienna, Austria : 1996) 2006 Oct 113 (10): 1499-509. Wang H K, Fung H C, Hsu W C, Wu Y R, Lin J C, Ro L S, Chang K H, Hwu F J, Hsu Y, Huang S Y, Lee-Chen G J, Chen C |
| A coding polymorphism of the kallikrein 1 gene is associated with essential hypertension: a tagging SNP-based association study in a Chinese Han population. Journal of hypertension 2007 Sep 25 (9): 1821-7. Zhao Weiyan, Wang Laiyuan, Lu Xiangfeng, Yang Wei, Huang Jianfeng, Chen Shufeng, Gu Dongfe |
| Association of functional kallikrein-1 promoter polymorphisms and acute kidney injury: a case-control and longitudinal cohort study. Nephron. Clinical practice 2012 122 (3-4): 107-13. Susantitaphong Paweena, Perianayagam Mary C, Kang Sun Woo, Zhang Wenyi, Rao Fangwen, O'Connor Daniel T, Jaber Bertrand |
| Relationship between the gene polymorphisms of kallikrein-kinin system and Alzheimer's disease in a Hunan Han Chinese population. International journal of clinical and experimental pathology 2015 8 (12): 15550-62. Deng Yanyao, Hou Deren, Tian Mi, Li Wei, Feng Xialu, Yu Zhuli |
| Novel risk genes and mechanisms implicated by exome sequencing of 2572 individuals with pulmonary arterial hypertension. Genome medicine 2019 Nov 11 (1): 69. Zhu Na, Pauciulo Michael W, Welch Carrie L, Lutz Katie A, Coleman Anna W, Gonzaga-Jauregui Claudia, Wang Jiayao, Grimes Joseph M, Martin Lisa J, He Hua, , Shen Yufeng, Chung Wendy K, Nichols William |
| Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE). Frontiers in allergy 2022 7 3 868185. Parsopoulou Faidra, Loules Gedeon, Zamanakou Maria, Csuka Dorottya, Szilagyi Agnes, Kompoti Maria, Porebski Grzegorz, Psarros Fotis, Magerl Markus, Valerieva Anna, Staevska Maria, Obtulowicz Krystyna, Maurer Marcus, Speletas Matthaios, Farkas Henriette, Germenis Anastasios |
| Analysis of the association of ANO3/MUC15, COL4A4, RRBP1, and KLK1 polymorphisms with COPD susceptibility in the Kashi population. BMC pulmonary medicine 2022 May 22 (1): 178. Tang Lifeng, Zhong Xuemei, Gong Hui, Tuerxun Maimaitiaili, Ma Tao, Ren Jie, Xie Chengxin, Zheng Aifang, Abudureheman Zulipikaer, Abudukadeer Ayiguzali, Aini Paierda, Yilamujiang Subinuer, Li |
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