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p53 codon 72 polymorphism and risk of cervical carcinoma in Korean women

Baek WK, Cho JW, Suh SI, Suh MH, Shin DH, Cho CH, Lee TS, Cha SD

A common polymorphism of the wild type p53 is known at codon 72 of exon 4, with 2 alleles encoding either arginine (CGC, p53Arg) or proline (CCC, p53Pro). A recent...
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Polymorphism of the CYP1A1 and glutathione-S-transferase gene in Korean lung cancer patients

Hong YS, Chang JH, Kwon OJ, Ham YA, Choi JH

  • KMID: 755008
  • Exp Mol Med.
  • 1998 Dec;30(4):192-198.
The levels of expressions and catalytic activities of cytochrome P450 (CYP1A1) and glutathione-S-transferase class mu (GSTM1) enzymes in lungs and their metabolic balance may be an important determinant host factor underlying lung cancer....
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Association of the ACE gene polymorphism with the progression of autosomal dominant polycystic kidney disease

Lee KB, Kim UK, Lee CC

Renin-angiotensin system is considered important in the genesis of hypertension and development of end-stage renal disease (ESRD) in autosomal dominant polycystic kidney disease (ADPKD). The angiotensin converting enzyme (ACE) gene...
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The Roles of Stromelysin-1 and the Gelatinase B Gene Polymorphism in Stable Angina

Kim JS, Park HY, Kwon JH, Im EK, Choi D, Jang Y, Cho SY

Matrix metalloproteinases contribute to vascular remodeling by breaking down extracellular-matrix while new matrix is synthesized. Of the variety of MMPs, stromelysin-1 and gelatinase B may have key roles in coronary...
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A Single Nucleotide Polymorphism in the E-cadherin Gene Promoter-160 is Not Associated with Risk of Korean Gastric Cancer

Park WS, Cho YG, Park JY, Kim CJ, Lee JH, Kim HS, Lee JW, Song YH, Park CH, Park YK, Kim SY, Nam SW, Lee SH, Yoo NJ, Lee JY

Recently, the -160 C/A polymorphism, located within the regulatory region of E-cadherin promoter, has been shown to influence E-cadherin transcription by altering transcription factor binding. We examined the effect of...
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Apolipoprotein E polymorphism in non-diabetic patients with acute coronary syndrome

Kim IJ, Hong BK, Lee BK, Kwon HM, Kim D, Choi EY, Byun KH, Kim JH, Song KS, Kim HS

Since a decade ago, apolipoprotein (apo) E polymorphism has been focussed as a risk factor for cardiovascular disease. ApoE plays a central role as a receptor ligand for...
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The angiotensin converting enzyme genetic polymorphism in acute coronary syndrome--ACE polymorphism as a risk factor of acute coronary syndrome

Park HY, Kwon HM, Kim D, Jang Y, Shim WH, Cho SY, Kim HS

The deletion polymorphism of angiotensin converting enzyme (ACE) genotype has been reported as an independent risk factor for the development of myocardial infarction (MI). However there are conflicting data...
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Lack of Relationship between Vitamin D Receptor Polymorphism and Bone Erosion in Rheumatoid Arthritis

Lee CK, Hong JS, Cho YS, Yoo B, Kim GS, Moon HB

We performed this study to investigate the possible association between vitamin D receptor (VDR) gene polymorphism and the focal bone erosion in rheumatoid arthritis (RA) patients in Korea. One hundred...
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Tissue Plasminogen Activator and Plasminogen Activator Inhibitor Type 1 Gene Polymorphism in Patients with Gastric Ulcer Complicated with Bleeding

Kim HS, Hwang KY, Chung IK, Park SH, Lee MH, Kim SJ, Hong SY

Tissue plasminogen activator (t-PA) and plasminogen activator inhibitor type 1 (PAI-1) may be involved in the pathogenesis of peptic ulcers through suppression of fibrinolysis. This study was designed to investigate...
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Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patients

Chaturvedi LS, Mukherjee , Srivastava S, Mittal RD, Mittal B

  • KMID: 1457538
  • Exp Mol Med.
  • 2001 Dec;33(4):251-256.
Duchenne and Becker muscular dystrophies (D/BMD) are caused by mutations in the dystrophin gene. Two-thirds of patients have large intragenic deletions or duplications and the remaining one-third have point mutations,...
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Angiotensin converting enzyme gene polym orphism in Korean patients with primary knee osteoarthritis

Hong SJ, Yang HI, Yoo MC, In CS, Yim SV, Jin SY, Choe BK, Chung JH

  • KMID: 1094700
  • Exp Mol Med.
  • 2003 Jun;35(3):189-195.
Angiotensin converting enzyme (ACE) plays an important role in the physiology of vasculature, blood pressure and inflammation. ACE gene, known to have insertion/deletion (I/D) polymorphism, has been widely investigated in...
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GSTP1 Polymorphism, Cigarette Smoking and Cervical Cancer Risk in Korean Women

Jee SH, Lee JE, Kim S, Kim JH, Um SJ, Lee SJ, Namkoong S, Park JS

Previous studies have suggested that glutathione S-transferase (GST) genotypes may play a role in determining susceptibility to cervical cancer, though the data have often been conflicting. The objective of this...
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Analysis of polymorphic region of GAM-1 gene in Plasmodium vivax Korean isolates

Kho WG, Chung JY, Hwang UW, Chun JH, Park YH, Chung WC

The identification, characterization and quantification of Plasmodium sp. genetic polymorphism are becoming increasingly important in the vaccine development. We investigated polymorphism of Plasmodium vivax GAM-1 (PvGAM-1) gene in 30 Korean...
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NRAMP1 gene polymorphisms in patients with rheumatoid arthritis in Koreans

Yang YS, Kim SJ, Kim JW, Koh EM

Natural resistance-associated macrophage protein 1 (Nramp1) is a genetic locus associated with innate resistance or susceptibility of murine hosts to infection with intracellular pathogens such as Salmonella, Leishmania and Mycobacterium....
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Tumor Necrosis Factor-alpha Levels and Promoter Polymorphism in Patients with Kawasaki Disease in Korea

Ahn SY, Jang GC, Shin JS, Shin KM, Kim DS

Tumor necrosis factor (TNF) -alpha plays a major role in the pathogenesis of Kawasaki disease (KD), a systemic vasculitis primarily affecting young children. We performed this study to examine the...
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Association of Angiotensin-Converting Enzyme and Angiotensinogen Gene Polymorphisms with Preeclampsia

Choi H, Kang JY, Yoon HS, Han SS, Whang CS, Moon IG, Shin HH, Park JB

We tested the hypothesis that angiotensin-converting enzyme (ACE) and angiotensinogen gene polymorphism influence the incidence, development and outcome of preeclampsia. Subjects were recruited from 90 Korean patients with preeclampsia during...
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Evaluation of a Apo-1/Fas promoter polymorphism in Korean stroke patients

Seo JC, Han SW, Yin CS, Koh HK, Kim CH, Kim EH, Leem KH, Lee HS, Park HJ, Kim SA, Choe BK, Lee HJ, Yim SV, Kim CJ, Chung JH

  • KMID: 931880
  • Exp Mol Med.
  • 2002 Sep;34(4):294-298.
Apoptosis has been implicated in the pathogenesis of neurodegenerative diseases such as stroke and Alzheimer's disease. Apo-1/Fas gene is one of the mediators of apoptosis in stroke. MvaI polymorphism...
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Homozygous VN (677C to T) and d/D (2756G to A) variants in the methylenetetrahydrofolate and methionine synthase genes in a case of hyperhomocysteinemia with stroke at young age

Song KS, Song JW, Choi JR, Kim HK, Shin JS, Kim JH

  • KMID: 1085748
  • Exp Mol Med.
  • 2001 Jun;33(2):106-109.
Hyperhomocysteinemia is known to be associated with an increased risk of myocardial infarction, stroke, peripheral arterial disease, and venous thrombosis. Gene polymorphisms in methylenetetrahydrofolate reductase (MTHFR) and methionine synthase (MS)...
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Relation of Apolipoprotein E Polymorphism to Clinically Diagnosed Fatty Liver Disease

Lee DM, Lee SO, Mun BS, Ahn HS, Park HY, Lee HS, Kim DG

  • KMID: 863110
  • Korean J Hepatol.
  • 2002 Dec;8(4):355-362.
BACKGROUND/AIMS: Apolipoprotein E (Apo E) is important in plasma lipid metabolism and is a component of several plasma lipoprotein-lipid particles. Three major Apo E isoforms are encoded by three...
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Effects of Val34Leu and Val35Leu polymorphism on the enzyme activity of the coagulation factor XIII-A

Lee IH, Chung SI, Lee SY

  • KMID: 755212
  • Exp Mol Med.
  • 2002 Nov;34(5):385-390.
Change in fibrin stabilizing activity of factor XIII A subunit (FXIII-A) caused by a specific mutation, Val34Leu, is recently implicated to incidences of pathophysiology of thrombosis. In an effort to...
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