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Results 1 - 20 of 54  for All Library Resources

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1
Unveiling Genetic Variants Underlying Vitamin D Deficiency in Multiple Korean Cohorts by a Genome-Wide Association Study
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Unveiling Genetic Variants Underlying Vitamin D Deficiency in Multiple Korean Cohorts by a Genome-Wide Association Study

Endocrinology and Metabolism, 2021, 36(6), , pp.1189-1200 [Peer Reviewed Journal]

Copyright © 2021 Korean Endocrine Society 2021 ;ISSN: 2093-596X ;EISSN: 2093-5978 ;DOI: 10.3803/EnM.2021.1241 ;PMID: 34852423

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2
Association between Alcohol Consumption and Serum Cortisol Levels: a Mendelian Randomization Study
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Association between Alcohol Consumption and Serum Cortisol Levels: a Mendelian Randomization Study

Journal of Korean Medical Science, 2021, 36(30), , pp.1-9 [Peer Reviewed Journal]

2021 The Korean Academy of Medical Sciences. ;2021 The Korean Academy of Medical Sciences. 2021 The Korean Academy of Medical Sciences ;ISSN: 1011-8934 ;EISSN: 1598-6357 ;DOI: 10.3346/jkms.2021.36.e195 ;PMID: 34342185

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3
IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis
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IL-10 Polymorphisms and Tuberculosis Susceptibility: An Updated Meta-Analysis

Yonsei Medical Journal, 2015, 56(5), , pp.1274-1287 [Peer Reviewed Journal]

Copyright: Yonsei University College of Medicine 2015 2015 ;ISSN: 0513-5796 ;EISSN: 1976-2437 ;DOI: 10.3349/ymj.2015.56.5.1274 ;PMID: 26256970

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4
DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population
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DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population

Annals of Laboratory Medicine, 2016, 36(2), , pp.145-153 [Peer Reviewed Journal]

The Korean Society for Laboratory Medicine. 2016 ;ISSN: 2234-3806 ;EISSN: 2234-3814 ;DOI: 10.3343/alm.2016.36.2.145 ;PMID: 26709262

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5
HLA Allele Frequencies in 5802 Koreans: Varied Allele Types Associated with SJS/TEN According to Culprit Drugs
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HLA Allele Frequencies in 5802 Koreans: Varied Allele Types Associated with SJS/TEN According to Culprit Drugs

Yonsei Medical Journal, 2016, 57(1), , pp.118-126 [Peer Reviewed Journal]

Copyright: Yonsei University College of Medicine 2016 2016 ;ISSN: 0513-5796 ;EISSN: 1976-2437 ;DOI: 10.3349/ymj.2016.57.1.118 ;PMID: 26632391

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6
Association between ALDH2 Polymorphism and Gastric Cancer Risk in a Korean Population
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Association between ALDH2 Polymorphism and Gastric Cancer Risk in a Korean Population

Journal of Korean Medical Science, 2020, 35(17), , pp.1-6 [Peer Reviewed Journal]

2020 The Korean Academy of Medical Sciences. ;2020 The Korean Academy of Medical Sciences. 2020 The Korean Academy of Medical Sciences ;ISSN: 1011-8934 ;EISSN: 1598-6357 ;DOI: 10.3346/jkms.2020.35.e148 ;PMID: 32356421

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7
Effects of CYP2C19 Genetic Polymorphisms on PK/PD Responses of Omeprazole in Korean Healthy Volunteers
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Effects of CYP2C19 Genetic Polymorphisms on PK/PD Responses of Omeprazole in Korean Healthy Volunteers

Journal of Korean Medical Science, 2017, 32(5), 227, pp.729-736 [Peer Reviewed Journal]

2017 The Korean Academy of Medical Sciences. ;2017 The Korean Academy of Medical Sciences. 2017 ;ISSN: 1011-8934 ;EISSN: 1598-6357 ;DOI: 10.3346/jkms.2017.32.5.729 ;PMID: 28378544

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8
Genetic Association for P2X7R rs3751142 and CARD8 rs2043211 Polymorphisms for Susceptibility of Gout in Korean Men: Multi-Center Study
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Genetic Association for P2X7R rs3751142 and CARD8 rs2043211 Polymorphisms for Susceptibility of Gout in Korean Men: Multi-Center Study

Journal of Korean Medical Science, 2016, 31(10), 220, pp.1566-1570 [Peer Reviewed Journal]

2016 The Korean Academy of Medical Sciences. 2016 ;ISSN: 1011-8934 ;EISSN: 1598-6357 ;DOI: 10.3346/jkms.2016.31.10.1566 ;PMID: 27550484

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9
Certain Polymorphisms in SP110 Gene Confer Susceptibility to Tuberculosis: A Comprehensive Review and Updated Meta-Analysis
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Certain Polymorphisms in SP110 Gene Confer Susceptibility to Tuberculosis: A Comprehensive Review and Updated Meta-Analysis

Yonsei Medical Journal, 2017, 58(1), , pp.165-173 [Peer Reviewed Journal]

Copyright: Yonsei University College of Medicine 2017 2017 ;ISSN: 0513-5796 ;EISSN: 1976-2437 ;DOI: 10.3349/ymj.2017.58.1.165 ;PMID: 27873510

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10
Development and Validation of a Novel Warfarin Dosing Algorithm for Korean Patients With VKORC1 1173C
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Development and Validation of a Novel Warfarin Dosing Algorithm for Korean Patients With VKORC1 1173C

Annals of Laboratory Medicine, 2020, 40(3), , pp.216-223 [Peer Reviewed Journal]

The Korean Society for Laboratory Medicine. ;The Korean Society for Laboratory Medicine 2020 The Korean Society for Laboratory Medicine ;ISSN: 2234-3806 ;EISSN: 2234-3814 ;DOI: 10.3343/alm.2020.40.3.216 ;PMID: 31858761

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11
ABCG2 Polymorphism Is Associated with Hyperuricemia in a Study of a Community-Based Korean Cohort
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ABCG2 Polymorphism Is Associated with Hyperuricemia in a Study of a Community-Based Korean Cohort

Journal of Korean Medical Science, 2017, 32(9), 231, pp.1451-1459 [Peer Reviewed Journal]

2017 The Korean Academy of Medical Sciences. ;2017 The Korean Academy of Medical Sciences. 2017 ;ISSN: 1011-8934 ;EISSN: 1598-6357 ;DOI: 10.3346/jkms.2017.32.9.1451 ;PMID: 28776340

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12
Replication of the results of genome-wide and candidate gene association studies on telomere length in a Korean population
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Replication of the results of genome-wide and candidate gene association studies on telomere length in a Korean population

The Korean Journal of Internal Medicine, 2015, 30(5), , pp.719-726 [Peer Reviewed Journal]

Copyright © 2015 The Korean Association of Internal Medicine 2015 ;ISSN: 1226-3303 ;EISSN: 2005-6648 ;DOI: 10.3904/kjim.2015.30.5.719 ;PMID: 26354067

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13
The FOXO1 Gene-Obesity Interaction Increases the Risk of Type 2 Diabetes Mellitus in a Chinese Han Population
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The FOXO1 Gene-Obesity Interaction Increases the Risk of Type 2 Diabetes Mellitus in a Chinese Han Population

Journal of Korean Medical Science, 2017, 32(2), 224, pp.264-271 [Peer Reviewed Journal]

2017 The Korean Academy of Medical Sciences. 2017 ;ISSN: 1011-8934 ;EISSN: 1598-6357 ;DOI: 10.3346/jkms.2017.32.2.264 ;PMID: 28049237

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14
Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses
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Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses

Annals of Laboratory Medicine, 2019, 39(6), , pp.545-551 [Peer Reviewed Journal]

The Korean Society for Laboratory Medicine. ;The Korean Society for Laboratory Medicine 2019 The Korean Society for Laboratory Medicine ;ISSN: 2234-3806 ;EISSN: 2234-3814 ;DOI: 10.3343/alm.2019.39.6.545 ;PMID: 31240882

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15
Single nucleotide polymorphisms of toll-like receptor 7 and toll-like receptor 9 in hepatitis C virus infection patients from central China
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Single nucleotide polymorphisms of toll-like receptor 7 and toll-like receptor 9 in hepatitis C virus infection patients from central China

Yonsei Medical Journal, 2014, 55(2), , pp.428-434 [Peer Reviewed Journal]

Copyright: Yonsei University College of Medicine 2014 2014 ;ISSN: 0513-5796 ;EISSN: 1976-2437 ;DOI: 10.3349/ymj.2014.55.2.428 ;PMID: 24532514

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16
An Analysis of the Filaggrin Gene Polymorphism in Korean Atopic Dermatitis Patients
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An Analysis of the Filaggrin Gene Polymorphism in Korean Atopic Dermatitis Patients

Journal of Korean Medical Science, 2016, 31(7), 217, pp.1136-1142 [Peer Reviewed Journal]

2016 The Korean Academy of Medical Sciences. 2016 ;ISSN: 1011-8934 ;EISSN: 1598-6357 ;DOI: 10.3346/jkms.2016.31.7.1136 ;PMID: 27366014

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17
The First Korean Family With Hereditary Gelsolin Amyloidosis Caused by p.D214Y Mutation in the GSN Gene
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The First Korean Family With Hereditary Gelsolin Amyloidosis Caused by p.D214Y Mutation in the GSN Gene

Annals of Laboratory Medicine, 2016, 36(3), , pp.259-262 [Peer Reviewed Journal]

The Korean Society for Laboratory Medicine. 2016 ;ISSN: 2234-3806 ;EISSN: 2234-3814 ;DOI: 10.3343/alm.2016.36.3.259 ;PMID: 26915616

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18
VEGF Promoter Polymorphism Confers an Increased Risk of Pulmonary Arterial Hypertension in a Chinese Population
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VEGF Promoter Polymorphism Confers an Increased Risk of Pulmonary Arterial Hypertension in a Chinese Population

Yonsei Medical Journal, 2017, 58(2), , pp.305-311 [Peer Reviewed Journal]

Copyright: Yonsei University College of Medicine 2017 2017 ;ISSN: 0513-5796 ;EISSN: 1976-2437 ;DOI: 10.3349/ymj.2017.58.2.305 ;PMID: 28120560

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19
Association of COL2A1 gene polymorphism with degenerative lumbar scoliosis
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Association of COL2A1 gene polymorphism with degenerative lumbar scoliosis

Clinics in Orthopedic Surgery, 2014, 6(4), , pp.379-384 [Peer Reviewed Journal]

Copyright © 2014 by The Korean Orthopaedic Association 2014 ;ISSN: 2005-291X ;EISSN: 2005-4408 ;DOI: 10.4055/cios.2014.6.4.379 ;PMID: 25436060

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20
Mutation Analysis of the TGFBI Gene in Consecutive Korean Patients With Corneal Dystrophies
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Mutation Analysis of the TGFBI Gene in Consecutive Korean Patients With Corneal Dystrophies

Annals of Laboratory Medicine, 2015, 35(3), , pp.336-340 [Peer Reviewed Journal]

The Korean Society for Laboratory Medicine. 2015 ;ISSN: 2234-3806 ;EISSN: 2234-3814 ;DOI: 10.3343/alm.2015.35.3.336 ;PMID: 25932442

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