Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: PRKCH[original query] |
---|
Polymorphisms in inflammation-related genes are associated with susceptibility to major depression and antidepressant response. Molecular psychiatry 2008 Aug 13 (8): 800-12. Wong M-L, Dong C, Maestre-Mesa J, Licinio |
Association of the genetic variants of APOA5 and PRKCH with hypertension in community-dwelling Japanese individuals. Molecular medicine reports 0 1 (3): 407-14. Yamada Yoshiji, Ando Fujiko, Shimokata Hiros |
[Genetic risk factors of ischemic stroke identified by a genome-wide association study]. Brain and nerve = Shinkei kenky? no shinpo 2008 Nov 60 (11): 1339-46. Kubo Michia |
Association between PRKCH gene polymorphisms and subcortical silent brain infarction. Atherosclerosis 2008 Aug 199 (2): 340-5. Serizawa M, Nabika T, Ochiai Y, Takahashi K, Yamaguchi S, Makaya M, Kobayashi S, Kato |
Association of PRKCH gene with lacunar infarction in a local Chinese Han population. Neuroscience letters 2009 Oct 464 (2): 146-9. Cheng Hong, Wang Feng, Ding Xinsheng, Ding Haixia, Song Xinji |
The 1425G/A SNP in PRKCH is associated with ischemic stroke and cerebral hemorrhage in a Chinese population. Stroke; a journal of cerebral circulation 2009 Sep 40 (9): 2973-6. Wu Lijun, Shen Yue, Liu Xin, Ma Xu, Xi Bo, Mi Jie, Lindpaintner Klaus, Tan Xuerui, Wang Xing |
[Molecular epidemiology of cerebrovascular diseases; the Hisayama study and the Fukuoka Stroke Registry (FSR)]. Rinsh? shinkeigaku = Clinical neurology 2008 Nov 48 (11): 892-5. Kitazono Takanari, Kubo Michiaki, Hata Jun, Ibayashi Setsuro, Kiyohara Yutaka, Iida Mits |
PRKCH gene polymorphism is associated with the risk of severe gastric atrophy. Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2010 Jun 13 (2): 90-4. Goto Yasuyuki, Hishida Asahi, Matsuo Keitaro, Tajima Kazuo, Morita Emi, Naito Mariko, Wakai Kenji, Hamajima Nobuyu |
Contribution of 1425G/A polymorphism in protein kinase C-Eta (PRKCH) gene and brain white matter lesions to the risk of sudden sensorineural hearing loss in a Japanese nested case-control study. Journal of neurogenetics 2011 Oct 25 (3): 82-7. Uchida Yasue, Sugiura Saiko, Nakashima Tsutomu, Ando Fujiko, Shimokata Hiros |
The role of PRKCH gene variants in coronary artery disease in a Chinese population. Molecular biology reports 2012 Feb 39 (2): 1777-82. Zhu Jun, Yan Jian-Jun, Kuai Zheng-Ping, Gao Wei, Tang Jian-Jin, Jia En-Zhi, Yang Zhi-Jian, Wang Lian-She |
Identification of homogeneous genetic architecture of multiple genetically correlated traits by block clustering of genome-wide associations. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2011 Jun 26 (6): 1261-71. Gupta Mayetri, Cheung Ching-Lung, Hsu Yi-Hsiang, Demissie Serkalem, Cupples L Adrienne, Kiel Douglas P, Karasik Dav |
Autosome-wide copy number variation association analysis for rheumatoid arthritis using the WTCCC high-density SNP genotype data. The Journal of rheumatology 2011 May 38 (5): 797-801. Uddin Mohammed, Sturge Mitch, Rahman Proton, Woods Michael |
[Genome-wide association study for ischemic stroke based on the Hisayama study]. Nihon eiseigaku zasshi. Japanese journal of hygiene 2011 Jan 66 (1): 47-52. Hata Jun, Kubo Michiaki, Kiyohara Yuta |
Association between 1425G/A SNP in PRKCH and ischemic stroke among Chinese and Japanese populations: a meta-analysis including 3686 cases and 4589 controls. Neuroscience letters 2012 Jan 506 (1): 55-8. Li Jiaoxing, Luo Man, Xu Xiaowei, Sheng Wen |
Protein kinase C? polymorphism and the susceptibilities to intracerebral hemorrhage in the Taiwan population. Neuroscience letters 2012 Oct 528 (2): 170-3. Chen Yi-Chun, Chen Phoebe, Wu Yih-Ru, Shie Shian-Sen, Chen Sien-Tsong, Lee-Chen Guey-Jen, Chen Chiung-M |
The SNP (rs2230500) in PRKCH decreases the risk of carotid intima-media thickness in a Chinese young adult population. PloS one 2012 7 (7): e40606. Wu Lijun, Xi Bo, Hou Dongqing, Zhao Xiaoyuan, Liu Junting, Cheng Hong, Zhou Xin, Shen Yue, Wang Xingyu, Mi J |
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Nature genetics 2013 May 45 (5): 513-7. Wheeler Eleanor, Huang Ni, Bochukova Elena G, Keogh Julia M, Lindsay Sarah, Garg Sumedha, Henning Elana, Blackburn Hannah, Loos Ruth J F, Wareham Nick J, O'Rahilly Stephen, Hurles Matthew E, Barroso Inês, Farooqi I Sad |
Impact of the 1425G/A polymorphism of PRKCH on the recurrence of ischemic stroke: Fukuoka Stroke Registry. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2014 Jul 23 (6): 1356-61. Matsuo Ryu, Ago Tetsuro, Hata Jun, Kuroda Junya, Wakisaka Yoshinobu, Sugimori Hiroshi, Kitazono Takanari, Kamouchi Masahiro, |
PRKCH 1425G/A Polymorphism Predicts Recurrence of Ischemic Stroke in a Chinese Population. Molecular neurobiology 2014 Nov . Zhang Zhizhong, Xu Gelin, Zhu Wusheng, Cao Liping, Yan Bernard, Liu Xinfe |
A quantitative assessment of the association between 1425G/A polymorphism in PRKCH and risk of stroke. Neuromolecular medicine 2014 Dec 16 (4): 814-20. Sun Lingli, Zhang Zhizhong, Ma Minmin, Xu Gelin, Liu Xinfe |
Protein kinase C? polymorphism and the susceptibility to ischemic stroke in the Taiwan population. Biomedical journal 2015 Apr . Chen Yi-Chun, Huang Chi-Jui, Chen Phoebe, Wu Yih-Ru, Shie Shian-Sen, Chen Sien-Tsong, Lee-Chen Guey-Jen, Chen Chiung-M |
DGKH genetic risk variant influences gene expression in bipolar affective disorder. Journal of affective disorders 2016 Jul 198 148-57. Kittel-Schneider Sarah, Lorenz Carina, Auer Joyce, Weißflog Lena, Reif Andre |
SOD1 gene polymorphisms in sudden sensorineural hearing loss. Acta oto-laryngologica 2016 Feb 1-5. Kitoh Ryosuke, Nishio Shin-Ya, Ogawa Kaoru, Okamoto Makito, Kitamura Ken, Gyo Kiyofumi, Sato Hiroaki, Nakashima Tsutomu, Fukuda Satoshi, Fukushima Kunihiro, Hara Akira, Yamasoba Tatsuya, Usami Shin-Ic |
Influence of PRKCH gene polymorphism on antihypertensive response to amlodipine and telmisartan. Clinical and experimental hypertension (New York, N.Y. : 1993) 2017 Jun 1-6. Zhang Zan-Ling, Zhu Miao-Miao, Li Hui-Lan, Shi Li-Hong, Chen Xiao-Ping, Luo Jia, Zhao Jin-Fe |
Genetic association between 1425G/A SNP in PRKCH and hypertrophic cardiomyopathy in a Chinese population. Oncotarget 2017 Dec 8 (70): 114839-114844. Ji Feng, Liu Qun, Feng Zeyu, Han Xinwei, Li Zhito |
PRKCH polymorphism is associated with rheumatoid arthritis in a Chinese population. Bioscience trends 2019 Dec . Zhuang Yue, Di Yanan, Huang Lulin, Zhu Ji |
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. medRxiv : the preprint server for health sciences 2020 Nov . Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph |
Genetic signature of human longevity in PKC and NF-?B signaling. Aging cell 2021 7 20 (7): e13362. Ryu Seungjin, Han Jeehae, Norden-Krichmar Trina M, Zhang Quanwei, Lee Seunggeun, Zhang Zhengdong, Atzmon Gil, Niedernhofer Laura J, Robbins Paul D, Barzilai Nir, Schork Nicholas J, Suh Yous |
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. Alzheimer's & dementia : the journal of the Alzheimer's Association 2021 Apr . Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, , Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph |
Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD. Hepatology communications 2021 4 5 (4): 598-607. Wegermann Kara, Garrett Melanie E, Zheng Jiayin, Coviello Andrea, Moylan Cynthia A, Abdelmalek Manal F, Chow Shein-Chung, Guy Cynthia D, Diehl Anna Mae, Ashley-Koch Allison, Suzuki Aya |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: