Differential SIRT1 Expression in Hepatocellular Carcinomas and Cholangiocarcinoma of the Liver
Beta-catenin Expression Patterns in Matched Pre- and Post-Neoadjuvant Chemotherapy-Resistant Breast Cancer
Fibroblast Growth Factor 23 Predicts Coronary Calcification and Poor Prognosis in Patients with Chronic Kidney Disease Stages 3–5D
Prevalence of Howell-Jolly Body-Like Inclusions in HIV Patients and Their Correlation with CD4 Counts and HIV RNA Viral Load
Everolimus Method Comparison between Waters MassTrak™ Immunosuppressants XE (IUO) Kit and an In-house Laboratory Developed LC-MS/MS Method in Renal Transplant Patients
Identification of Mycobacterium tuberculosis and Rifampin Resistance in Clinical Specimens Using the Xpert MTB/RIF Assay
Immune Responses to a Recombinant Rv0057-Rv1352 Fusion Protein of Mycobacterium tuberculosis
Association between Serum Free Thyroxine (FT4) and Uric Acid Levels in Populations without Overt Thyroid Dysfunction
Serum Myosin Light Chain Kinase in Type 2 Diabetes Mellitus: a Cross-Sectional Study
Effect of Small Interference RNA on the Acetylcholine-Sensitive Potassium Channel in H9c2 Cells
Selection of Superior Reference Genes’ Combination for Quantitative Real-time PCR in B-cell Lymphomas
T-cell/Histiocyte-Rich Large B-cell Lymphoma in Pediatric Patients: an Under-Recognized Entity?
The Utility of B-cell Receptor Gene Rearrangement Studies in Diagnosing Diffuse Large B-cell Lymphoma with Plasmacytic Differentiation
Congenital Peribronchial Myofibroblastic Tumor: Case Report of an Asymptomatic Infant with a Rapidly Enlarging Pulmonary Mass and Review of the Literature
A Novel Splice Site Mutation in the PAX6 Gene in a Korean Family with Isolated Aniridia
Mutation Screening in Candidate Genes in Four Chinese Brachydactyly Families
Osteogenesis Imperfecta Type I Caused by a Novel Mutation in the Start Codon of the COL1A1 Gene in a Korean Family
A Case Report of a Fetus with Mosaic Autosomal Variegated Aneuploidies and Literature Review
A Novel NOTCH2 Mutation Identified in a Korean Family with Hajdu-Cheney Syndrome Showing Phenotypic Diversity
Letter to the Editor: A Working Model for Real Time Quality Assurance in Anatomic Pathology