133 related articles for article (PubMed ID: 29383124)
1. Genetic association between 1425G/A SNP in PRKCH and hypertrophic cardiomyopathy in a Chinese population.
Ji F; Liu Q; Feng Z; Han X; Li Z
Oncotarget; 2017 Dec; 8(70):114839-114844. PubMed ID: 29383124
[TBL] [Abstract][Full Text] [Related]
2. The 1425G/A SNP in PRKCH is associated with ischemic stroke and cerebral hemorrhage in a Chinese population.
Wu L; Shen Y; Liu X; Ma X; Xi B; Mi J; Lindpaintner K; Tan X; Wang X
Stroke; 2009 Sep; 40(9):2973-6. PubMed ID: 19520989
[TBL] [Abstract][Full Text] [Related]
3. Association between 1425G/A SNP in PRKCH and ischemic stroke among Chinese and Japanese populations: a meta-analysis including 3686 cases and 4589 controls.
Li J; Luo M; Xu X; Sheng W
Neurosci Lett; 2012 Jan; 506(1):55-8. PubMed ID: 22044875
[TBL] [Abstract][Full Text] [Related]
4. Protein kinase Cη polymorphism and the susceptibilities to intracerebral hemorrhage in the Taiwan population.
Chen YC; Chen P; Wu YR; Shie SS; Chen ST; Lee-Chen GJ; Chen CM
Neurosci Lett; 2012 Oct; 528(2):170-3. PubMed ID: 22999931
[TBL] [Abstract][Full Text] [Related]
5. A quantitative assessment of the association between 1425G/A polymorphism in PRKCH and risk of stroke.
Sun L; Zhang Z; Ma M; Xu G; Liu X
Neuromolecular Med; 2014 Dec; 16(4):814-20. PubMed ID: 25272991
[TBL] [Abstract][Full Text] [Related]
6. PRKCH 1425G/A Polymorphism Predicts Recurrence of Ischemic Stroke in a Chinese Population.
Zhang Z; Xu G; Zhu W; Cao L; Yan B; Liu X
Mol Neurobiol; 2015 Dec; 52(3):1648-1653. PubMed ID: 25370935
[TBL] [Abstract][Full Text] [Related]
7. Protein kinase Cη polymorphism and the susceptibility to ischemic stroke in the Taiwan population.
Chen YC; Huang CJ; Chen P; Wu YR; Shie SS; Chen ST; Lee-Chen GJ; Chen CM
Biomed J; 2015; 38(5):433-8. PubMed ID: 25900926
[TBL] [Abstract][Full Text] [Related]
8. Impact of the 1425G/A polymorphism of PRKCH on the recurrence of ischemic stroke: Fukuoka Stroke Registry.
Matsuo R; Ago T; Hata J; Kuroda J; Wakisaka Y; Sugimori H; Kitazono T; Kamouchi M;
J Stroke Cerebrovasc Dis; 2014 Jul; 23(6):1356-61. PubMed ID: 24534126
[TBL] [Abstract][Full Text] [Related]
9. 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.
Uchida Y; Sugiura S; Nakashima T; Ando F; Shimokata H
J Neurogenet; 2011 Oct; 25(3):82-7. PubMed ID: 21756056
[TBL] [Abstract][Full Text] [Related]
10. Genetic association between the PRKCH gene encoding protein kinase Ceta isozyme and rheumatoid arthritis in the Japanese population.
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
Arthritis Rheum; 2007 Jan; 56(1):30-42. PubMed ID: 17195206
[TBL] [Abstract][Full Text] [Related]
11. [Mode of splitting of the second heart sound in patients with hypertrophic cardiomyopathy].
Fukuda N; Oki T; Sakai H; Asai M; Ohshima C; Kusaka Y; Tominaga T; Murao A; Niki T; Mori H
J Cardiogr; 1983 Jun; 13(2):327-41. PubMed ID: 6687124
[TBL] [Abstract][Full Text] [Related]
12. Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.
Kubo T; Gimeno JR; Bahl A; Steffensen U; Steffensen M; Osman E; Thaman R; Mogensen J; Elliott PM; Doi Y; McKenna WJ
J Am Coll Cardiol; 2007 Jun; 49(25):2419-26. PubMed ID: 17599605
[TBL] [Abstract][Full Text] [Related]
13. Relationship of basal-septal fibrosis with LV outflow tract obstruction in hypertrophic cardiomyopathy: insights from cardiac magnetic resonance analysis.
Nakamura T; Iwanaga Y; Yasuda M; Kawamura T; Miyaji Y; Morooka H; Miyazaki S
Int J Cardiovasc Imaging; 2016 Apr; 32(4):613-20. PubMed ID: 26589516
[TBL] [Abstract][Full Text] [Related]
14. Myocardial fibrosis in patients with symptomatic obstructive hypertrophic cardiomyopathy: correlation with echocardiographic measurements, sarcomeric genotypes, and pro-left ventricular hypertrophy polymorphisms involving the renin-angiotensin-aldosterone system.
Blauwet LA; Ackerman MJ; Edwards WD; Riehle DL; Ommen SR
Cardiovasc Pathol; 2009; 18(5):262-8. PubMed ID: 18835191
[TBL] [Abstract][Full Text] [Related]
15. A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction.
Kubo M; Hata J; Ninomiya T; Matsuda K; Yonemoto K; Nakano T; Matsushita T; Yamazaki K; Ohnishi Y; Saito S; Kitazono T; Ibayashi S; Sueishi K; Iida M; Nakamura Y; Kiyohara Y
Nat Genet; 2007 Feb; 39(2):212-7. PubMed ID: 17206144
[TBL] [Abstract][Full Text] [Related]
16. Association of PRKCH gene with lacunar infarction in a local Chinese Han population.
Cheng H; Wang F; Ding X; Ding H; Song X
Neurosci Lett; 2009 Oct; 464(2):146-9. PubMed ID: 19703523
[TBL] [Abstract][Full Text] [Related]
17. Myocardial mechanical remodeling after septal myectomy for severe obstructive hypertrophic cardiomyopathy.
Moravsky G; Bruchal-Garbicz B; Jamorski M; Ralph-Edwards A; Gruner C; Williams L; Woo A; Yang H; Laczay B; Rakowski H; Carasso S
J Am Soc Echocardiogr; 2013 Aug; 26(8):893-900. PubMed ID: 23800507
[TBL] [Abstract][Full Text] [Related]
18. NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy.
Earle N; Ingles J; Bagnall RD; Gray B; Crawford J; Smith W; Shelling AN; Love DR; Semsarian C; Skinner JR
J Cardiovasc Electrophysiol; 2015 Dec; 26(12):1346-51. PubMed ID: 26332198
[TBL] [Abstract][Full Text] [Related]
19. Association Between Genetic Variation in the SCN10A Gene and Cardiac Conduction Abnormalities in Patients With Hypertrophic Cardiomyopathy.
Iio C; Ogimoto A; Nagai T; Suzuki J; Inoue K; Nishimura K; Uetani T; Okayama H; Okura T; Shigematsu Y; Tabara Y; Kohara K; Miki T; Hamada M; Higaki J
Int Heart J; 2015; 56(4):421-7. PubMed ID: 26104176
[TBL] [Abstract][Full Text] [Related]
20. PKCη deficiency improves lipid metabolism and atherosclerosis in apolipoprotein E-deficient mice.
Torisu K; Zhang X; Nonaka M; Kaji T; Tsuchimoto D; Kajitani K; Sakumi K; Torisu T; Chida K; Sueishi K; Kubo M; Hata J; Kitazono T; Kiyohara Y; Nakabeppu Y
Genes Cells; 2016 Oct; 21(10):1030-1048. PubMed ID: 27545963
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]