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YUHSpace1. College of Medicine (의과대학)Dept. of Pharmacology (약리학교실)

1. Journal Papers

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Issue DateTitleJournal Title
2017A novel missense mutation in NR0B1 causes delayed-onset primary adrenal insufficiency in adultsCLINICAL GENETICS
2017Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome JOURNAL OF CLINICAL INVESTIGATION
2017Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report BMC MEDICAL GENETICS
2017ANO9/TMEM16J promotes tumourigenesis via EGFR and is a novel therapeutic target for pancreatic cancerBRITISH JOURNAL OF CANCER
2017Targeted Genome Engineering to Control VEGF Expression in Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells: Potential Implications for the Treatment of Myocardial Infarction STEM CELLS TRANSLATIONAL MEDICINE
2017RanBPM: a potential therapeutic target for modulating diverse physiological disordersDRUG DISCOVERY TODAY
2017Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus SyndromeJAMA OPHTHALMOLOGY
2017NLRP3 Inflammasome Contributes to Lipopolysaccharide-induced Depressive-Like Behaviors via Indoleamine 2,3-dioxygenase Induction INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY
2017Glutamatergic stimulation of the left dentate gyrus abolishes depressive-like behaviors in a rat learned helplessness paradigmNEUROIMAGE
2017Changes in brain metabolic connectivity underlie autistic-like social deficits in a rat model of autism spectrum disorder SCIENTIFIC REPORTS
2017Chronological Change of Right Ventricle by Chronic Intermittent Hypoxia in MiceSLEEP
2017Oxytocin receptor gene polymorphisms exert a modulating effect on the onset age in patients with obsessive-compulsive disorderPSYCHONEUROENDOCRINOLOGY
2017Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly NATURE GENETICS
2017Constriction of the mitochondrial inner compartment is a priming event for mitochondrial division. NATURE COMMUNICATIONS
2017Cystic kidneys in fetal Walker-Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literatureAMERICAN JOURNAL OF MEDICAL GENETICS PART A
2017Ezetimibe ameliorates steatohepatitis via AMP activated protein kinase-TFEB-mediated activation of autophagy and NLRP3 inflammasome inhibitionAUTOPHAGY
2017Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract INVESTIGATIVE AND CLINICAL UROLOGY
2017A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBDGUT
2017Oncogenic BRAF fusions in mucosal melanomas activate the MAPK pathway and are sensitive to MEK/PI3K inhibition or MEK/CDK4/6 inhibitionONCOGENE
2017Green Teeth Associated Hyperbilirubinemia in Primary Dentition Journal of the Korean Academy of Pediatric Dentistry (대한소아치과학회지)
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