YUHSpace: Dept. of Pharmacology (약리학교실)

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

Dept. of Pharmacology (약리학교실)

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Highly Cited Articles

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 Date	Title	Journal Title
2019	β-catenin activation down-regulates cell-cell junction-related genes and induces epithelial-to-mesenchymal transition in colorectal cancers	SCIENTIFIC REPORTS
2019	Assessment of mGluR5 KO mice under conditions of low stress using a rodent touchscreen apparatus reveals impaired behavioural flexibility driven by perseverative responses	Molecular Brain
2019	A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators	HUMAN MUTATION
2019	Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis	NATURE COMMUNICATIONS
2019	Programmable Nuclease-Based Integration into Novel Extragenic Genomic Safe Harbor Identified from Korean Population-Based CNV Analysis	Molecular Therapy Oncolytics
2019	Low binding affinity and reduced complement-dependent cell death efficacy of ofatumumab produced using a plant system (Nicotiana benthamiana L.)	PROTEIN EXPRESSION AND PURIFICATION
2019	En bloc and segmental deletions of human XIST reveal X chromosome inactivation-involving RNA elements	NUCLEIC ACIDS RESEARCH
2019	The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report	BMC MEDICAL GENETICS
2019	Reduced expression of pyruvate kinase in kidney proximal tubule cells is a potential mechanism of pravastatin altered glucose metabolism	SCIENTIFIC REPORTS
2019	Predicting Disease Progression in Patients with Bicuspid Aortic Stenosis Using Mathematical Modeling	Journal of Clinical Medicine
2019	Temperature-dependent increase in the calcium sensitivity and acceleration of activation of ANO6 chloride channel variants	Scientific Reports
2019	A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction	EUROPEAN JOURNAL OF MEDICAL GENETICS
2019	Contribution of SLC22A12 on hypouricemia and its clinical significance for screening purposes	SCIENTIFIC REPORTS
2018	Aβ pathology downregulates brain mGluR5 density in a mouse model of Alzheimer	NEUROPHARMACOLOGY
2018	Deep learning improves prediction of CRISPR-Cpf1 guide RNA activity	NATURE BIOTECHNOLOGY
2018	Population PK-PD Model of Pegylated Interferon Alfa-2a in Healthy Korean Men	JOURNAL OF PHARMACEUTICAL SCIENCES
2018	Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss	SCIENTIFIC REPORTS
2018	Novel association between CDKAL1 and cholesterol efflux capacity: Replication after GWAS-based discovery	ATHEROSCLEROSIS
2018	Mechanistic Model for Blood Pressure and Heart Rate Changes Produced by Telmisartan in Human Beings	BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
2018	Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis	KIDNEY INTERNATIONAL