Browsing by Keyword : Genetic Variation

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Showing results 6 to 26 of 26

Pub YearTitleAuthor(s)
2015Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene.손영배
2019Differences in Expression of Human Leukocyte Antigen Class II Subtypes and T Cell Subsets in Behcet's Disease with Arthritis김현아, 서창희, 손성향, 정주양
2014Exonic variants associated with development of aspirin exacerbated respiratory diseases.박해심
2010Functional variability of the adenosine A3 receptor (ADORA3) gene polymorphism in aspirin-induced urticaria.김승현, 박해심, 예영민
2017Genetic variants of the gasdermin B gene associated with the development of aspirin-exacerbated respiratory diseases박해심
2017Identification and Functional Characterization of ST3GAL5 and ST8SIA1 Variants in Patients with Thyroid-Associated Ophthalmopathy국경훈
2004Identification of a novel HLA-B*55 variant (B*5513) from a Korean family.박해심
2018Identification of genomic aberrations associated with lymph node metastasis in diffuse-type gastric cancer김영배, 우현구, 이다근, 최지혜, 한상욱
2020Identification of Novel Genetic Variants Related to Trabecular Bone Score in Community-Dwelling Older Adults조남한
2019Maternal Perinatal Dietary Patterns Affect Food Allergy Development in Susceptible Infants이수영
2021Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus서창희
2018Nonsynonymous Variants in PAX4 and GLP1R Are Associated With Type 2 Diabetes in an East Asian Population조남한
1999Participation of the melanocortin-1 receptor in the UV control of pigmentation.임성빈
2018Population genetic structure and natural selection of Plasmodium falciparum apical membrane antigen-1 in Myanmar isolates신호준
2010Prevalence and diversity of carbapenemases among imipenem-nonsusceptible Acinetobacter isolates in Korea: emergence of a novel OXA-182.이위교
2012Prioritization of SNPs for genome-wide association studies using an interaction model of genetic variation, gene expression, and trait variation백효정
2011Replicated association between genetic variation in the PARK2 gene and blood pressure.정선용, 진현석
2010Spondylo-epiphyseal dysplasia, Maroteaux type (pseudo-Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations.김옥화
2020SWATH-MS analysis of cerebrospinal fluid to generate a robust battery of biomarkers for Alzheimer's disease박범희, 박선아
2006The 11482G >A polymorphism in the perilipin gene is associated with weight gain with rosiglitazone treatment in type 2 diabetes.김혜진
1995Variability of in vivo recovery of factor IX after infusion of monoclonal antibody purified factor IX concentrates in patients with hemophilia B. The Mononine Study Group.김효철
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