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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Disease and PRKCH[original query]
Genetic association between the PRKCH gene encoding protein kinase Ceta isozyme and rheumatoid arthritis in the Japanese population.
Arthritis and rheumatism 2007 Jan 56 (1): 30-42.
Takata Y, Hamada D, Miyatake K, Nakano S, Shinomiya F, Scafe CR, Reeve VM, Osabe D, Moritani M, Kunika K, Kamatani N, Inoue H, Yasui N, Itakura M
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
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
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
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
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
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