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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
2020	Regulation of CFTR Bicarbonate Channel Activity by WNK1: Implications for Pancreatitis and CFTR-Related Disorders	CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY
2020	Effect of dapagliflozin, a sodium-glucose co-transporter-2 inhibitor, on gluconeogenesis in proximal renal tubules	DIABETES OBESITY & METABOLISM
2020	High-throughput analysis of the activities of xCas9, SpCas9-NG and SpCas9 at matched and mismatched target sequences in human cells	NATURE BIOMEDICAL ENGINEERING
2020	Dynamic predictive model for postoperative nausea and vomiting for intravenous fentanyl patient-controlled analgesia	ANAESTHESIA
2020	Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation	EAR AND HEARING
2019	LIN28A loss of function is associated with Parkinson's disease pathogenesis	EMBO JOURNAL
2019	PANCREATITIS-ASSOCIATED PROTEIN-1 SUPPRESSES APOPTOSIS IN CERULEIN-STIMULATED PANCREATIC ACINAR CELLS IN RESPONSE TO NUCLEAR FACTOR-KAPPA B ACTIVATION	JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
2019	Diminished food-related motivation in adult rats treated with methamphetamine during adolescence	NEUROREPORT
2019	Functional Characterization of Pharmcogenetic Variants of Human Cytochrome P450 2C9 in Korean Populations	BIOMOLECULES & THERAPEUTICS
2019	Mutations of ADAMTS9 Cause Nephronophthisis-Related Ciliopathy	AMERICAN JOURNAL OF HUMAN GENETICS
2019	Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis	NATURE COMMUNICATIONS
2019	Autism-like behaviors in male mice with a Pcdh19 deletion	MOLECULAR BRAIN
2019	Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis	Human Genetics
2019	Optimal Dosing Regimen of Phenytoin for Korean Epilepsy Patients: From Premature Babies to the Elderly	Journal of Pharmaceutical Sciences
2019	Programmable Nuclease-Based Integration into Novel Extragenic Genomic Safe Harbor Identified from Korean Population-Based CNV Analysis	Molecular Therapy Oncolytics
2019	Therapeutic application of the CRISPR system: current issues and new prospects	Human Genetics
2019	Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency	Scientific Reports
2019	Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment	Experimental and Molecular Medicine
2019	En bloc and segmental deletions of human XIST reveal X chromosome inactivation-involving RNA elements	NUCLEIC ACIDS RESEARCH
2019	Reduced expression of pyruvate kinase in kidney proximal tubule cells is a potential mechanism of pravastatin altered glucose metabolism	SCIENTIFIC REPORTS

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