Detalhe da pesquisa
1.
A genome-wide association study of a coronary artery disease risk variant.
J Hum Genet
; 58(3): 120-6, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23364394
2.
Genetic variants in the IL12B gene are associated with inflammatory bowel diseases in the Korean population.
J Gastroenterol Hepatol
; 28(10): 1588-94, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23573954
3.
Common variants in RYR1 are associated with left ventricular hypertrophy assessed by electrocardiogram.
Eur Heart J
; 33(10): 1250-6, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21828061
4.
Association of a genetic variant of BTN2A1 with metabolic syndrome in East Asian populations.
J Med Genet
; 48(11): 787-92, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21784758
5.
A novel mutation in the SCN5A gene is associated with Brugada syndrome.
Life Sci
; 80(8): 716-24, 2007 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-17141278
6.
Genetic polymorphism in the pregnancy-associated plasma protein-A associated with acute myocardial infarction.
Coron Artery Dis
; 18(6): 417-22, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17700210
7.
Cordycepin inhibits lipopolysaccharide-induced inflammation by the suppression of NF-kappaB through Akt and p38 inhibition in RAW 264.7 macrophage cells.
Eur J Pharmacol
; 545(2-3): 192-9, 2006 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-16899239
8.
Forensic genetic analysis of mitochondrial DNA hypervariable region I/II sequences: an expanded Korean population database.
Forensic Sci Int
; 158(2-3): 125-30, 2006 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-15990264
9.
Association between Serine/Threonine Kinase 39 Gene Polymorphism, Hypertension, and Other Cardiovascular Risk Factors in Koreans.
Korean Circ J
; 43(1): 13-22, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23408757
10.
Association between CDH13 variants and cardiometabolic and vascular phenotypes in a Korean population.
Yonsei Med J
; 54(6): 1305-12, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24142632
11.
Adiponectin and progression of arterial stiffness in hypertensive patients.
Int J Cardiol
; 163(3): 316-319, 2013 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21724272
12.
Associations between genetic variants in the IRGM gene and inflammatory bowel diseases in the Korean population.
Inflamm Bowel Dis
; 19(1): 106-14, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22508677
13.
Association of CYP2C19*2 and *3 genetic variants with essential hypertension in Koreans.
Yonsei Med J
; 53(6): 1113-9, 2012 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23074110
14.
The Relationship Between Gastric Myoelectric Activity and SCN5A Mutation Suggesting Sodium Channelopathy in Patients With Brugada Syndrome and Functional Dyspepsia - A Pilot Study.
J Neurogastroenterol Motil
; 18(1): 58-63, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22323988
15.
The relationship between insulin-like growth factor-1 and metabolic syndrome, independent of adiponectin.
Clin Chim Acta
; 413(3-4): 506-10, 2012 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22133783
16.
Synergistic effects of genetic variants of APOA5 and BTN2A1 on dyslipidemia or metabolic syndrome.
Int J Mol Med
; 30(1): 185-92, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22576629
17.
Association of cytochrome P450 2C19*2 polymorphism with clopidogrel response variability and cardiovascular events in Koreans treated with drug-eluting stents.
Heart
; 98(2): 139-44, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21700758
18.
High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea.
Investig Genet
; 2(1): 10, 2011 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-21463511
19.
Association of a polymorphism of BTN2A1 with dyslipidemia in East Asian populations.
Exp Ther Med
; 2(4): 745-749, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22977569
20.
Relationships between genetic polymorphisms of triggering receptor expressed on myeloid cells-1 and inflammatory bowel diseases in the Korean population.
Life Sci
; 89(9-10): 289-94, 2011 Aug 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-21763322