Dept. of Pharmacology (약리학교실)

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STIM1 carboxyl-terminus activates native SOC, Icrac and TRPC1 channels

Guo N. Huang ; Weizhong Zeng ; Joo Young Kim ; Joseph P. Yuan ; Linhuang Han ... NATURE CELL BIOLOGY, Vol.8(9) : 1003-1010, 2006

Autistic-like social behaviour in Shank2-mutant mice improved by restori...

Hyejung Won ; Hye-Ryeon Lee ; Heon Yung Gee ; Won Mah ; Jae-Ick Kim ; Jiseok ... NATURE, Vol.486(7402) : 261-265, 2012

Dynamic association of proteasomal machinery with the centrosome

W. Christian Wigley ; Rosalind P. Fabunmi ; Min Goo Lee ; Christopher R. Mari... JOURNAL OF CELL BIOLOGY, Vol.145(3) : 481-490, 1999
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Issue DateTitleJournal Title
2017Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency JOURNAL OF CLINICAL INVESTIGATION
2017Biological efficacy of two mineral trioxide aggregate (MTA)-based materials in a canine model of pulpotomy DENTAL MATERIALS JOURNAL
2017Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical DysplasiaAMERICAN JOURNAL OF HUMAN GENETICS
2017Optimizing reproducibility of operant testing through reinforcer standardization: identification of key nutritional constituents determining reward strength in touchscreens MOLECULAR BRAIN
2017Hippocampus-Dependent Goal Localization by Head-Fixed Mice in Virtual Reality ENEURO
2017Adopting automated image analysis tool for fibrin network: Can we obtain clot properties for practical application?INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
2017소아에서 비전형적인 임상양상을 보인 스피츠모반 1예Korean Journal of Dermatology (대한피부과학회지)
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
2017Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease NATURE GENETICS
2017Oncogenic BRAF fusions in mucosal melanomas activate the MAPK pathway and are sensitive to MEK/PI3K inhibition or MEK/CDK4/6 inhibitionONCOGENE
2017A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBDGUT
2017Green Teeth Associated Hyperbilirubinemia in Primary Dentition Journal of the Korean Academy of Pediatric Dentistry (대한소아치과학회지)
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
2017Constriction of the mitochondrial inner compartment is a priming event for mitochondrial division. NATURE COMMUNICATIONS
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
2017Glutamatergic stimulation of the left dentate gyrus abolishes depressive-like behaviors in a rat learned helplessness paradigmNEUROIMAGE
2017Ezetimibe ameliorates steatohepatitis via AMP activated protein kinase-TFEB-mediated activation of autophagy and NLRP3 inflammasome inhibitionAUTOPHAGY
2017Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly NATURE GENETICS

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