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YUHSpace1. College of Medicine (의과대학)Dept. of Pharmacology (약리학교실)1. Journal Papers

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Issue Date	Title	Journal Title
2017	Concise Review: Fate Determination of Stem Cells by Deubiquitinating Enzymes	STEM CELLS
2017	Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population	SCIENTIFIC REPORTS
2017	A Review of Modeling Approaches to Predict Drug Response in Clinical Oncology	YONSEI MEDICAL JOURNAL
2017	Quantitative Assessment of Food Effect on the Pharmacokinetics of Nano-Crystallized Megestrol Acetate	BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
2017	UDP-Induced Phagocytosis and ATP-Stimulated Chemotactic Migration Are Impaired in STIM1-/- Microglia In Vitro and In Vivo	MEDIATORS OF INFLAMMATION
2017	Sec16A is critical for both conventional and unconventional secretion of CFTR	SCIENTIFIC REPORTS
2017	Targeted Next-Generation Sequencing for Comprehensive Genetic Profiling of Pharmacogenes	CLINICAL PHARMACOLOGY & THERAPEUTICS
2017	Relationships between Psychosocial Difficulties and Oxidative Stress Biomarkers in Women Subject to Intimate Partner Violence	HEALTH & SOCIAL WORK
2017	Adult-Onset Vitelliform Macular Dystrophy caused by BEST1 p.Ile38Ser Mutation is a Mild Form of Best Vitelliform Macular Dystrophy	SCIENTIFIC REPORTS
2017	Oxytocin receptor gene polymorphisms exert a modulating effect on the onset age in patients with obsessive-compulsive disorder	PSYCHONEUROENDOCRINOLOGY
2017	Glutamatergic stimulation of the left dentate gyrus abolishes depressive-like behaviors in a rat learned helplessness paradigm	NEUROIMAGE
2017	MPSR1 is a cytoplasmic PQC E3 ligase for eliminating emergent misfolded proteins in Arabidopsis thaliana	PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
2017	Changes in brain metabolic connectivity underlie autistic-like social deficits in a rat model of autism spectrum disorder	SCIENTIFIC REPORTS
2017	Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome	JAMA OPHTHALMOLOGY
2017	Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly	NATURE GENETICS
2017	Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease	NATURE GENETICS
2017	Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract	INVESTIGATIVE AND CLINICAL UROLOGY
2017	RanBPM: a potential therapeutic target for modulating diverse physiological disorders	DRUG DISCOVERY TODAY
2017	Sustained Mutant KIT Activation in the Golgi Complex Is Mediated by PKC-θ in Gastrointestinal Stromal Tumors	CLINICAL CANCER RESEARCH
2017	Chronological Change of Right Ventricle by Chronic Intermittent Hypoxia in Mice	SLEEP

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