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
2019Autism-like behaviors in male mice with a Pcdh19 deletion MOLECULAR BRAIN
2019Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairmentExperimental and Molecular Medicine
2019Programmable Nuclease-Based Integration into Novel Extragenic Genomic Safe Harbor Identified from Korean Population-Based CNV Analysis Molecular Therapy Oncolytics
2019Optimal Dosing Regimen of Phenytoin for Korean Epilepsy Patients: From Premature Babies to the ElderlyJournal of Pharmaceutical Sciences
2019Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency Scientific Reports
2019Therapeutic application of the CRISPR system: current issues and new prospectsHuman Genetics
2019Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasisHuman Genetics
2019Low binding affinity and reduced complement-dependent cell death efficacy of ofatumumab produced using a plant system (Nicotiana benthamiana L.)PROTEIN EXPRESSION AND PURIFICATION
2019Predicting Disease Progression in Patients with Bicuspid Aortic Stenosis Using Mathematical Modeling Journal of Clinical Medicine
2019The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report BMC MEDICAL GENETICS
2019Reduced expression of pyruvate kinase in kidney proximal tubule cells is a potential mechanism of pravastatin altered glucose metabolism SCIENTIFIC REPORTS
2019Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndromeKIDNEY INTERNATIONAL
2019Contribution of SLC22A12 on hypouricemia and its clinical significance for screening purposes SCIENTIFIC REPORTS
2019Hyperpolarized [1-13C]lactate flux increased in the hippocampal region in diabetic mice MOLECULAR BRAIN
2019SpCas9 activity prediction by DeepSpCas9, a deep learning-based model with high generalization performance Science Advances
2019β-catenin activation down-regulates cell-cell junction-related genes and induces epithelial-to-mesenchymal transition in colorectal cancers SCIENTIFIC REPORTS
2019Assessment of mGluR5 KO mice under conditions of low stress using a rodent touchscreen apparatus reveals impaired behavioural flexibility driven by perseverative responses Molecular Brain
2019Temperature-dependent increase in the calcium sensitivity and acceleration of activation of ANO6 chloride channel variants Scientific Reports
2019A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunctionEUROPEAN JOURNAL OF MEDICAL GENETICS
2019A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activatorsHUMAN MUTATION

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