about
Increased expression and localization of a serine protease inhibitor, protease nexin-1 (PN-1), in the ovary and uterus during implantation in ratAssociation of rs2075575 and rs9951307 polymorphisms of AQP-4 gene with leukoaraiosis.ADAMTS13 gene mutations in children with hemolytic uremic syndrome.miR-27a and miR-449b polymorphisms associated with a risk of idiopathic recurrent pregnancy lossThe GC + CC genotype at position -418 in TIMP-2 promoter and the -1575GA/-1306CC genotype in MMP-2 is genetic predisposing factors for prevalence of moyamoya diseaseThe role of VEGF and KDR polymorphisms in moyamoya disease and collateral revascularization.Genetic variants in 3'-UTRs of methylenetetrahydrofolate reductase (MTHFR) predict colorectal cancer susceptibility in Koreans.Gender-specific association between polymorphism of vascular endothelial growth factor (VEGF 936C>T) gene and patients with stomach cancerAssociation study of five functional polymorphisms in matrix metalloproteinase-2, -3, and -9 genes with risk of primary ovarian insufficiency in Korean women.Polymorphisms in tumor necrosis factor-alpha (-863C>A, -857C>T and +488G>A) are associated with idiopathic recurrent pregnancy loss in Korean women.Association of methionine synthase and thymidylate synthase genetic polymorphisms with idiopathic recurrent pregnancy loss.Single nucleotide polymorphisms at miR-146a/196a2 and their primary ovarian insufficiency-related target gene regulation in granulosa cellsInterplay between 3'-UTR polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene and the risk of ischemic stroke.Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase in squamous cell carcinoma and basal cell carcinoma of the skin.Polymorphisms in the DNA repair gene XRCC1 associated with basal cell carcinoma and squamous cell carcinoma of the skin in a Korean population.Effect of methylenetetrahydrofolate reductase and thymidylate synthase enhancer region polymorphisms on the risk of idiopathic recurrent spontaneous abortion in a Korean population.The relationships between endothelial nitric oxide synthase polymorphisms and the formation of intracranial aneurysms in the Korean population.Association of transforming growth factor-beta 1 gene polymorphism with genetic susceptibility to ossification of the posterior longitudinal ligament in Korean patients.Association of the miR-146aC>G, miR-149T>C, miR-196a2T>C, and miR-499A>G polymorphisms with gastric cancer risk and survival in the Korean population.Influence of combined methylenetetrahydrofolate reductase (MTHFR) and thymidylate synthase enhancer region (TSER) polymorphisms to plasma homocysteine levels in Korean patients with recurrent spontaneous abortion.Association between folate metabolism-related gene polymorphisms and methylation of p16(INK4A) and hMLH1 genes in spontaneously aborted embryos with normal chromosomal integrity.The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea.Association of methylenetetrahydrofolate reductase (MTHFR 677C>T) and thymidylate synthase (TSER and TS 1494del6) polymorphisms with premature ovarian failure in Korean women.Association of the miR-146a, miR-149, miR-196a2, and miR-499 polymorphisms with ischemic stroke and silent brain infarction risk.Thymic carcinoma with brain metastasis mimicking meningioma.Preimplantation diagnosis of non-deletion Duchenne muscular dystrophy (DMD) by linkage polymerase chain reaction analysis.Association of kinase insert domain-containing receptor (KDR) gene polymorphisms with idiopathic recurrent spontaneous abortion in Korean women.Association between polymorphisms in renin-angiotensin system genes and primary ovarian insufficiency in Korean women.3'-UTR Polymorphisms of MTHFR and TS Associated with Osteoporotic Vertebral Compression Fracture Susceptibility in Postmenopausal Women.The 677C>T mutation of the MTHFR gene increases the risk of venous thromboembolism in Koreans and a meta-analysis from Asian population.Deficiency of von Willebrand factor-cleaving protease activity in the plasma of malignant patients.Transcobalamin II (TCN2 67A>G and TCN2 776C>G) and transcobalamin II receptor (TCblR 1104C>T) polymorphisms in Korean patients with idiopathic recurrent spontaneous abortion.Association of VEGF and KDR single nucleotide polymorphisms with colorectal cancer susceptibility in Koreans.Association between kinase insert domain-containing receptor polymorphisms (-604T>C, 1192G>A, 1719A>T) and premature ovarian failure in Korean women.Solute Carrier Family 19, member 1 (SLC19A1) polymorphisms (-43T>C, 80G>A, and 696C>T), and haplotypes in idiopathic recurrent spontaneous abortion in a Korean population.Inheritance of Charcot-Marie-Tooth disease 1A with rare nonrecurrent genomic rearrangement.The luteinizing hormone beta-subunit exon 3 (Gly102Ser) gene mutation is rare in Korean women with endometriosis and polycystic ovary syndromePrevalent genotypes of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) in spontaneously aborted embryosAssociation study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertilityAssociation study of vascular endothelial growth factor polymorphisms with the risk of recurrent spontaneous abortion
P50
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P50
description
onderzoeker
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researcher
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հետազոտող
@hy
name
Nam Keun Kim
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Nam Keun Kim
@en
Nam Keun Kim
@es
Nam Keun Kim
@nl
Nam Keun Kim
@sl
type
label
Nam Keun Kim
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Nam Keun Kim
@en
Nam Keun Kim
@es
Nam Keun Kim
@nl
Nam Keun Kim
@sl
prefLabel
Nam Keun Kim
@ast
Nam Keun Kim
@en
Nam Keun Kim
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Nam Keun Kim
@nl
Nam Keun Kim
@sl
P106
P108
P1153
35074187200
P31
P496
0000-0003-0541-3528