YUHSpace: 1. Journal Papers

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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
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	Optimal Dosing Regimen of Phenytoin for Korean Epilepsy Patients: From Premature Babies to the Elderly	Journal of Pharmaceutical Sciences
2019	Therapeutic application of the CRISPR system: current issues and new prospects	Human Genetics
2019	Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment	Experimental and Molecular Medicine
2019	Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency	Scientific Reports
2019	Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis	Human Genetics
2019	Temperature-dependent increase in the calcium sensitivity and acceleration of activation of ANO6 chloride channel variants	Scientific Reports
2019	En bloc and segmental deletions of human XIST reveal X chromosome inactivation-involving RNA elements	NUCLEIC ACIDS RESEARCH
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	Overexpression and Implications of Melanoma-associated Antigen A12 in Pathogenesis of Human Cutaneous Squamous Cell Carcinoma	ANTICANCER RESEARCH
2019	Reduced expression of pyruvate kinase in kidney proximal tubule cells is a potential mechanism of pravastatin altered glucose metabolism	SCIENTIFIC REPORTS
2019	The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report	BMC MEDICAL GENETICS
2018	Population pharmacokinetic model of levetiracetam in Korean neonates with seizures	INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS
2019	Mutations of ADAMTS9 Cause Nephronophthisis-Related Ciliopathy	AMERICAN JOURNAL OF HUMAN GENETICS
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	A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction	EUROPEAN JOURNAL OF MEDICAL GENETICS
2018	Rapid-Onset Obesity with Hypoventilation, Hypothalamic, Autonomic Dysregulation, and Neuroendocrine Tumors (ROHHADNET) Syndrome: A Systematic Review	BIOMED RESEARCH INTERNATIONAL
2018	Population PK-PD Model of Pegylated Interferon Alfa-2a in Healthy Korean Men	JOURNAL OF PHARMACEUTICAL SCIENCES
2018	Hyperpolarized [1-13C] pyruvate MR spectroscopy detect altered glycolysis in the brain of a cognitively impaired mouse model fed high-fat diet	MOLECULAR BRAIN
2017	소아에서 비전형적인 임상양상을 보인 스피츠모반 1예	Korean Journal of Dermatology (대한피부과학회지)

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