Lista de obras - Nam Keun Kim - Dominio Público Uruguay

3'-UTR Polymorphisms in the Vascular Endothelial Growth Factor Gene (VEGF) Contribute to Susceptibility to Recurrent Pregnancy Loss (RPL)

scientific article published on 05 July 2019

3'-UTR Polymorphisms of MTHFR and TS Associated with Osteoporotic Vertebral Compression Fracture Susceptibility in Postmenopausal Women.

artículo científico publicado en 2018

3'-UTR Polymorphisms of Vitamin B-Related Genes Are Associated with Osteoporosis and Osteoporotic Vertebral Compression Fractures (OVCFs) in Postmenopausal Women

scientific article published on 02 June 2020

MiR-10a, 27a, 34b/c, and 300 Polymorphisms are Associated with Ischemic Stroke Susceptibility and Post-Stroke Mortality

scientific article published on 25 November 2020

ADAMTS13 gene mutations in children with hemolytic uremic syndrome

artículo científico publicado en 2011

Analysis of the Association Between MicroRNA Biogenesis Gene Polymorphisms and Venous Thromboembolism in Koreans

scientific article published on 01 August 2019

Association between Five Common Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphisms and Colorectal Cancer Susceptibility

artículo científico publicado en 2020

Association between Platelet-Specific Collagen Receptor Glycoprotein 6 Gene Variants, Selected Biomarkers, and Recurrent Pregnancy Loss in Korean Women

artículo científico publicado en 2020

Association between folate metabolism-related gene polymorphisms and methylation of p16(INK4A) and hMLH1 genes in spontaneously aborted embryos with normal chromosomal integrity

artículo científico publicado en 2008

Association between kinase insert domain-containing receptor polymorphisms (-604T>C, 1192G>A, 1719A>T) and premature ovarian failure in Korean women.

artículo científico publicado en 2012

Association between polymorphisms in renin-angiotensin system genes and primary ovarian insufficiency in Korean women.

artículo científico publicado en 2013

Association of VEGF and KDR single nucleotide polymorphisms with colorectal cancer susceptibility in Koreans ⬇️

artículo científico publicado el 20 de noviembre de 2012

Association of an APBA3 Missense Variant with Risk of Premature Ovarian Failure in the Korean Female Population

artículo científico publicado en 2020

Association of kinase insert domain-containing receptor (KDR) gene polymorphisms with idiopathic recurrent spontaneous abortion in Korean women

artículo científico publicado en 2012

Association of methionine synthase and thymidylate synthase genetic polymorphisms with idiopathic recurrent pregnancy loss ⬇️

artículo científico publicado el 14 de febrero de 2013

Association of methylenetetrahydrofolate reductase (MTHFR 677C>T) and thymidylate synthase (TSER and TS 1494del6) polymorphisms with premature ovarian failure in Korean women

artículo científico publicado en 2012

Association of rs2075575 and rs9951307 polymorphisms of AQP-4 gene with leukoaraiosis.

artículo científico publicado en 2014

Association of the miR-146a , miR-149 , miR-196a2 , and miR-499 Polymorphisms With Ischemic Stroke and Silent Brain Infarction Risk ⬇️

artículo científico publicado el 29 de noviembre de 2012

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

artículo científico publicado en 2012

Association of transforming growth factor-beta 1 gene polymorphism with genetic susceptibility to ossification of the posterior longitudinal ligament in Korean patients

artículo científico publicado en 2013

Association study of AGO1 and AGO2 genes polymorphisms with recurrent pregnancy loss

artículo científico publicado en 2019

Association study of five functional polymorphisms in matrix metalloproteinase-2, -3, and -9 genes with risk of primary ovarian insufficiency in Korean women

artículo científico publicado en 2014

Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility

artículo científico publicado en 2006

Association study of vascular endothelial growth factor polymorphisms with the risk of recurrent spontaneous abortion

artículo científico publicado en 2009

Correction: Kim, N.K., et al. Study of the Association between microRNA (miR-25T>C, miR-32C>A, miR-125C>T, and miR-222G>T) Polymorphisms and the Risk of Recurrent Pregnancy Loss in Korean Women. Genes 2020, 11, 354

artículo científico publicado en 2020

Deficiency of von Willebrand factor-cleaving protease activity in the plasma of malignant patients.

artículo científico publicado en 2002

Distribution of Intracranial Major Artery Stenosis/Occlusion According to RNF213 Polymorphisms

artículo científico publicado en 2020

Effect of methylenetetrahydrofolate reductase and thymidylate synthase enhancer region polymorphisms on the risk of idiopathic recurrent spontaneous abortion in a Korean population

artículo científico publicado en 2008

Enhancing the Therapeutic Potential of CCL2-Overexpressing Mesenchymal Stem Cells in Acute Stroke

artículo científico publicado en 2020

Gender-specific association between polymorphism of vascular endothelial growth factor (VEGF 936C>T) gene and patients with stomach cancer

artículo científico publicado en 2008

Genetic polymorphisms of the cobalamin transport system are associated with idiopathic recurrent implantation failure

scientific article published on 23 May 2019

Genetic variants in 3'-UTRs of methylenetetrahydrofolate reductase (MTHFR) predict colorectal cancer susceptibility in Koreans.

artículo científico publicado en 2015

Increased expression and localization of a serine protease inhibitor, protease nexin-1 (PN-1), in the ovary and uterus during implantation in rat

scientific journal article

Influence of combined methylenetetrahydrofolate reductase (MTHFR) and thymidylate synthase enhancer region (TSER) polymorphisms to plasma homocysteine levels in Korean patients with recurrent spontaneous abortion

artículo científico publicado en 2005

Inheritance of Charcot-Marie-Tooth disease 1A with rare nonrecurrent genomic rearrangement.

artículo científico publicado en 2010

Interplay between 3'-UTR polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene and the risk of ischemic stroke

artículo científico publicado en 2017

MPG and NPRL3 Polymorphisms are Associated with Ischemic Stroke Susceptibility and Post-Stroke Mortality

scientific article published on 13 November 2020

Polymorphisms in the DNA repair gene XRCC1 associated with basal cell carcinoma and squamous cell carcinoma of the skin in a Korean population

artículo científico publicado en 2007

Polymorphisms in tumor necrosis factor-alpha (-863C>A, -857C>T and +488G>A) are associated with idiopathic recurrent pregnancy loss in Korean women

artículo científico publicado en 2016

Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase in squamous cell carcinoma and basal cell carcinoma of the skin ⬇️

artículo científico publicado el 8 de julio de 2010

Polymorphisms of platelet ADP receptor P2RY12 in the risk of venous thromboembolism in the Korean population

scientific article published on 23 January 2012

Preimplantation diagnosis of non-deletion Duchenne muscular dystrophy (DMD) by linkage polymerase chain reaction analysis

artículo científico publicado en 1998

Prevalent genotypes of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) in spontaneously aborted embryos

scientific article published on 13 November 2006

Single nucleotide polymorphisms at miR-146a/196a2 and their primary ovarian insufficiency-related target gene regulation in granulosa cells

artículo científico publicado en 2017

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.

artículo científico publicado en 2012

The 677C>T Mutation of the MTHFR Gene Increases the Risk of Venous Thromboembolism in Koreans and a Meta-Analysis From Asian Population ⬇️

artículo científico publicado el 12 de febrero de 2012

The 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 disease

artículo científico publicado en 2014

The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea

artículo científico publicado en 2017

The Role of VEGF and KDR Polymorphisms in Moyamoya Disease and Collateral Revascularization ⬇️

artículo científico publicado el 12 de octubre de 2012

The Synergistic Effect of Plasminogen Activator Inhibitor-1 (PAI-1) Polymorphisms and Metabolic Syndrome on Coronary Artery Disease in the Korean Population

artículo científico publicado en 2020

The luteinizing hormone beta-subunit exon 3 (Gly102Ser) gene mutation is rare in Korean women with endometriosis and polycystic ovary syndrome

artículo científico publicado en 2001

The relationships between endothelial nitric oxide synthase polymorphisms and the formation of intracranial aneurysms in the Korean population ⬇️

artículo científico publicado el 1 de junio de 2011

Thymic carcinoma with brain metastasis mimicking meningioma

artículo científico publicado en 2002

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.

artículo científico publicado en 2014

Vascular endothelial growth factor gene polymorphisms in Korean patients with premature ovarian failure

artículo científico publicado en 2011

miR-27a and miR-449b polymorphisms associated with a risk of idiopathic recurrent pregnancy loss

artículo científico publicado en 2017

Lista de obras de Nam Keun Kim

3'-UTR Polymorphisms in the Vascular Endothelial Growth Factor Gene (VEGF) Contribute to Susceptibility to Recurrent Pregnancy Loss (RPL)

3'-UTR Polymorphisms of MTHFR and TS Associated with Osteoporotic Vertebral Compression Fracture Susceptibility in Postmenopausal Women.

3'-UTR Polymorphisms of Vitamin B-Related Genes Are Associated with Osteoporosis and Osteoporotic Vertebral Compression Fractures (OVCFs) in Postmenopausal Women

<i>MiR-10a</i>, <i>27a</i>, <i>34b/c</i>, and <i>300</i> Polymorphisms are Associated with Ischemic Stroke Susceptibility and Post-Stroke Mortality

ADAMTS13 gene mutations in children with hemolytic uremic syndrome

Analysis of the Association Between MicroRNA Biogenesis Gene Polymorphisms and Venous Thromboembolism in Koreans

Association between Five Common Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphisms and Colorectal Cancer Susceptibility

Association between Platelet-Specific Collagen Receptor Glycoprotein 6 Gene Variants, Selected Biomarkers, and Recurrent Pregnancy Loss in Korean Women

Association between folate metabolism-related gene polymorphisms and methylation of p16(INK4A) and hMLH1 genes in spontaneously aborted embryos with normal chromosomal integrity

Association between kinase insert domain-containing receptor polymorphisms (-604T>C, 1192G>A, 1719A>T) and premature ovarian failure in Korean women.

Association between polymorphisms in renin-angiotensin system genes and primary ovarian insufficiency in Korean women.

Association of VEGF and KDR single nucleotide polymorphisms with colorectal cancer susceptibility in Koreans ⬇️

Association of an APBA3 Missense Variant with Risk of Premature Ovarian Failure in the Korean Female Population

Association of kinase insert domain-containing receptor (KDR) gene polymorphisms with idiopathic recurrent spontaneous abortion in Korean women

Association of methionine synthase and thymidylate synthase genetic polymorphisms with idiopathic recurrent pregnancy loss ⬇️

Association of methylenetetrahydrofolate reductase (MTHFR 677C>T) and thymidylate synthase (TSER and TS 1494del6) polymorphisms with premature ovarian failure in Korean women

Association of rs2075575 and rs9951307 polymorphisms of AQP-4 gene with leukoaraiosis.

Association of the miR-146a , miR-149 , miR-196a2 , and miR-499 Polymorphisms With Ischemic Stroke and Silent Brain Infarction Risk ⬇️

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

Association of transforming growth factor-beta 1 gene polymorphism with genetic susceptibility to ossification of the posterior longitudinal ligament in Korean patients

Association study of AGO1 and AGO2 genes polymorphisms with recurrent pregnancy loss

Association study of five functional polymorphisms in matrix metalloproteinase-2, -3, and -9 genes with risk of primary ovarian insufficiency in Korean women

Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility

Association study of vascular endothelial growth factor polymorphisms with the risk of recurrent spontaneous abortion

Correction: Kim, N.K., et al. Study of the Association between microRNA (miR-25T>C, miR-32C>A, miR-125C>T, and miR-222G>T) Polymorphisms and the Risk of Recurrent Pregnancy Loss in Korean Women. Genes 2020, 11, 354

Deficiency of von Willebrand factor-cleaving protease activity in the plasma of malignant patients.

Distribution of Intracranial Major Artery Stenosis/Occlusion According to RNF213 Polymorphisms

Effect of methylenetetrahydrofolate reductase and thymidylate synthase enhancer region polymorphisms on the risk of idiopathic recurrent spontaneous abortion in a Korean population

Enhancing the Therapeutic Potential of CCL2-Overexpressing Mesenchymal Stem Cells in Acute Stroke

Gender-specific association between polymorphism of vascular endothelial growth factor (VEGF 936C>T) gene and patients with stomach cancer

Genetic polymorphisms of the cobalamin transport system are associated with idiopathic recurrent implantation failure

Genetic variants in 3'-UTRs of methylenetetrahydrofolate reductase (MTHFR) predict colorectal cancer susceptibility in Koreans.

Increased expression and localization of a serine protease inhibitor, protease nexin-1 (PN-1), in the ovary and uterus during implantation in rat

Influence of combined methylenetetrahydrofolate reductase (MTHFR) and thymidylate synthase enhancer region (TSER) polymorphisms to plasma homocysteine levels in Korean patients with recurrent spontaneous abortion

Inheritance of Charcot-Marie-Tooth disease 1A with rare nonrecurrent genomic rearrangement.

Interplay between 3'-UTR polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene and the risk of ischemic stroke

MPG and NPRL3 Polymorphisms are Associated with Ischemic Stroke Susceptibility and Post-Stroke Mortality

Polymorphisms in the DNA repair gene XRCC1 associated with basal cell carcinoma and squamous cell carcinoma of the skin in a Korean population

Polymorphisms in tumor necrosis factor-alpha (-863C>A, -857C>T and +488G>A) are associated with idiopathic recurrent pregnancy loss in Korean women

Polymorphisms of 5,10-methylenetetrahydrofolate reductase and thymidylate synthase in squamous cell carcinoma and basal cell carcinoma of the skin ⬇️

Polymorphisms of platelet ADP receptor P2RY12 in the risk of venous thromboembolism in the Korean population

Preimplantation diagnosis of non-deletion Duchenne muscular dystrophy (DMD) by linkage polymerase chain reaction analysis

Prevalent genotypes of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) in spontaneously aborted embryos

Single nucleotide polymorphisms at miR-146a/196a2 and their primary ovarian insufficiency-related target gene regulation in granulosa cells

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.

The 677C&gt;T Mutation of the MTHFR Gene Increases the Risk of Venous Thromboembolism in Koreans and a Meta-Analysis From Asian Population ⬇️

The 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 disease

The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea

The Role of VEGF and KDR Polymorphisms in Moyamoya Disease and Collateral Revascularization ⬇️

The Synergistic Effect of Plasminogen Activator Inhibitor-1 (PAI-1) Polymorphisms and Metabolic Syndrome on Coronary Artery Disease in the Korean Population

The luteinizing hormone beta-subunit exon 3 (Gly102Ser) gene mutation is rare in Korean women with endometriosis and polycystic ovary syndrome

The relationships between endothelial nitric oxide synthase polymorphisms and the formation of intracranial aneurysms in the Korean population ⬇️

Thymic carcinoma with brain metastasis mimicking meningioma

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.

Vascular endothelial growth factor gene polymorphisms in Korean patients with premature ovarian failure

miR-27a and miR-449b polymorphisms associated with a risk of idiopathic recurrent pregnancy loss

The 677C>T Mutation of the MTHFR Gene Increases the Risk of Venous Thromboembolism in Koreans and a Meta-Analysis From Asian Population ⬇️