2015 | | A Dunnione Compound MB12662 Improves Cisplatin-Induced Tissue Injury and Emesis. | 박동선 |
2011 | | A Factor of Fasting Blood Glucose and Dietary Patterns in Korean Adults Using Data From the 2007, 2008 and 2009 Korea National Health and Nutrition Examination Survey | 전기홍 |
1996 | | A Familial Case Report of May-Hegglin Anomaly | 강원형, 임영애, 전희선 |
2008 | | A Family Case of Complete Androgen Insensitivity Syndrome in Sisters due to a Novel Mutation in the Androgen Receptor Gene | 김미란, 김현주, 정윤석, 주희재 |
2011 | | A fatal case of flufenoxuron-containing insecticide poisoning complicated by lactic acidosis, shock, abdominal compartment syndrome. | 민영기, 박은정, 최상천 |
2019 | | A feasibility study of laparoscopic total gastrectomy for clinical stage I gastric cancer: a prospective multi-center phase II clinical trial, KLASS 03 | 한상욱 |
2012 | | A fibrous stromal component in hepatocellular carcinoma reveals a cholangiocarcinoma-like gene expression trait and epithelial-mesenchymal transition | 김영배, 우현구 |
2009 | | A Floppy Baby with Congenital Myotonic Dystrophy Complicated with Huge Subgaleal Hematoma Occurring in Non-instrumental Vaginal Delivery | 이일영, 임신영 |
2015 | | A focal marked hypoechogenicity within an isoechoic thyroid nodule: is it a focal malignancy or not? | 하은주 |
2019 | | A formulated red ginseng extract inhibits autophagic flux and sensitizes to doxorubicin-induced cell death | 김유선 |
2013 | | A formulated red ginseng extract upregulates CHOP and increases TRAIL-mediated cytotoxicity in human hepatocellular carcinoma cells. | 김유선 |
2011 | | A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia. | 김옥화 |
2003 | | A Four-year Follow-up Case of Oligomeganephronia Detected Early by School Screening Urinalysis | - |
2021 | | A framework (SOCRATex) for hierarchical annotation of unstructured electronic health records and integration into a standardized medical database: Development and usability study | 노진, 박래웅, 정재연, 최진욱 |
2011 | | A functional promoter polymorphism of the human IL18 gene is associated with aspirin-induced urticaria. | 김승현, 박해심 |
2001 | | A Functional Study of Gap Junction in GJB2 Mutations Associated with Hereditary Hearing Loss | 박홍준, 이준호, 정연훈 |
2013 | | A genetic effect of IL-5 receptor α polymorphism in patients with aspirin-exacerbated respiratory disease. | 김승현, 박해심, 신유섭, 예영민 |
2013 | | A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. | 정재연, 조성원 |
2013 | | A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. | 조남한 |
2017 | | A Genome-Wide Association Study Identifies UTRN Gene Polymorphism for Restless Legs Syndrome in a Korean Population | 우현구, 최지혜 |