Browsing by Keyword : Genetic Variation

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Showing results 1 to 14 of 14

Publication YearTitleAJOU
Author
2013A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.정재연조성원
2008A polymorphism in the zinc transporter gene SLC30A8 confers resistance against posttransplantation diabetes mellitus in renal allograft recipients.한승진
2000Adaptive mutations in Sindbis virus E2 and Ross River virus E1 that allow efficient budding of chimeric viruses.김경민
2014Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations.서창희
2019Amino acid signatures of HLA Class-I and II molecules are strongly associated with SLE susceptibility and autoantibody production in Eastern Asians서창희
2010Functional variability of the adenosine A3 receptor (ADORA3) gene polymorphism in aspirin-induced urticaria.김승현예영민박해심
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
2019Maternal Perinatal Dietary Patterns Affect Food Allergy Development in Susceptible Infants이수영
1999Participation of the melanocortin-1 receptor in the UV control of pigmentation.임성빈
2010Prevalence and diversity of carbapenemases among imipenem-nonsusceptible Acinetobacter isolates in Korea: emergence of a novel OXA-182.이위교
2010Spondylo-epiphyseal dysplasia, Maroteaux type (pseudo-Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations.김옥화
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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