| 2017 | Enhancing inhibitory synaptic function reverses spatial memory deficits in Shank2 mutant mice | NEUROPHARMACOLOGY |
| 2017 | Targeted Next-Generation Sequencing for Comprehensive Genetic Profiling of Pharmacogenes | CLINICAL PHARMACOLOGY & THERAPEUTICS |
| 2017 | Sec16A is critical for both conventional and unconventional secretion of CFTR
| SCIENTIFIC REPORTS |
| 2017 | Sustained Mutant KIT Activation in the Golgi Complex Is Mediated by PKC-θ in Gastrointestinal Stromal Tumors | CLINICAL CANCER RESEARCH |
| 2016 | The clinical implication of single nucleotide polymorphisms in deoxycytidine kinase in chronic hepatitis B patients treated with lamivudine | JOURNAL OF MEDICAL VIROLOGY |
| 2016 | Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice
| NATURE COMMUNICATIONS |
| 2016 | Knockdown of RPL9 expression inhibits colorectal carcinoma growth via the inactivation of Id-1/NF-κB signaling axis | INTERNATIONAL JOURNAL OF ONCOLOGY |
| 2016 | Benefit of Adjuvant Chemotherapy After Curative Resection of Lung Metastasis in Colorectal Cancer | ANNALS OF SURGICAL ONCOLOGY |
| 2016 | Pilot Study of a Next-Generation Sequencing-Based Targeted Anticancer Therapy in Refractory Solid Tumors at a Korean Institution
| PLOS ONE |
| 2016 | Next-generation sequencing reveals somatic mutations that confer exceptional response to everolimus
| ONCOTARGET |
| 2016 | Generation of ΔF508-CFTR T84 cell lines by CRISPR/Cas9-mediated genome editing | BIOTECHNOLOGY LETTERS |
| 2016 | Resistance to pathologic cardiac hypertrophy and reduced expression of CaV1.2 in Trpc3-depleted mice | MOLECULAR AND CELLULAR BIOCHEMISTRY |
| 2016 | HLA-C*01 is a Risk Factor for Crohn's Disease | INFLAMMATORY BOWEL DISEASES |
| 2016 | Monomerization and ER Relocalization of GRASP Is a Requisite for Unconventional Secretion of CFTR | TRAFFIC |
| 2016 | SESN2/sestrin2 suppresses sepsis by inducing mitophagy and inhibiting NLRP3 activation in macrophages | AUTOPHAGY |
| 2016 | Prognostic Scoring Index for Patients with Metastatic Pancreatic Adenocarcinoma.
| CANCER RESEARCH AND TREATMENT |
| 2016 | Pore dilatation increases the bicarbonate permeability of CFTR, ANO1 and glycine receptor anion channels. | JOURNAL OF PHYSIOLOGY-LONDON |
| 2016 | Mutations in SLC26A1 Cause Nephrolithiasis. | AMERICAN JOURNAL OF HUMAN GENETICS |
| 2016 | The HSP70 co-chaperone DNAJC14 targets misfolded pendrin for unconventional protein secretion.
| NATURE COMMUNICATIONS |
| 2016 | Pharmacogenetic analysis of advanced non-small-cell lung cancer patients treated with first-line paclitaxel and carboplatin chemotherapy | PHARMACOGENETICS AND GENOMICS |
| 2016 | Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations
| YONSEI MEDICAL JOURNAL |
| 2015 | Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure | PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY |
| 2015 | A Novel BEST1 Mutation in Autosomal Recessive Bestrophinopathy | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE |
| 2015 | Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and Secretion | HUMAN MUTATION |
| 2015 | The full repertoire of Drosophila gustatory receptors for detecting an aversive compound
| NATURE COMMUNICATIONS |
| 2015 | Analysis of conventional and unconventional trafficking of CFTR and other membrane proteins | Methods in Molecular Biology (Clifton, N.J.) |
| 2015 | Benzopyrimido-pyrrolo-oxazine-dione (R)-BPO-27 Inhibits CFTR Chloride Channel Gating by Competition with ATP | MOLECULAR PHARMACOLOGY |
| 2015 | Non-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene
| EXPERIMENTAL AND MOLECULAR MEDICINE |
| 2015 | Regulation of phagocytosis and cytokine secretion by store-operated calcium entry in primary isolated murine microglia | CELLULAR SIGNALLING |
| 2015 | GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy | EPILEPSY RESEARCH |
| 2015 | Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis
| PLOS ONE |
| 2015 | Proprotein convertase 5/6a is associated with bone morphogenetic protein-2-induced squamous cell differentiation | AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY |
| 2015 | Targeted next-generation sequencing for the genetic diagnosis of dysferlinopathy | NEUROMUSCULAR DISORDERS |
| 2015 | Genetic testing of Korean familial hypercholesterolemia using whole-exome sequencing
| PLOS ONE |
| 2015 | microDuMIP: target-enrichment technique for microarray-based duplex molecular inversion probes
| NUCLEIC ACIDS RESEARCH |
| 2015 | Phase II clinical and exploratory biomarker study of dacomitinib in patients with recurrent and/or metastatic squamous cell carcinoma of head and neck | CLINICAL CANCER RESEARCH |
| 2015 | Does calmodulin regulate the bicarbonate permeability of ANO1/TMEM16A or not?
| JOURNAL OF GENERAL PHYSIOLOGY |
| 2014 | Identification of somatic mutations in EGFR/KRAS/ALK-negative lung adenocarcinoma in never-smokers
| GENOME MEDICINE |
| 2014 | Mechanisms of CFTR Functional Variants That Impair Regulated Bicarbonate Permeation and Increase Risk for Pancreatitis but Not for Cystic Fibrosis.
| PLOS GENETICS |
| 2014 | Role of calcium signaling in epithelial bicarbonate secretion | CELL CALCIUM |
| 2014 | Shank2 mutant mice display a hypersecretory response to cholera toxin | JOURNAL OF PHYSIOLOGY-LONDON |
| 2014 | Na+/H+ Exchanger Regulatory Factor 3 Is Critical for Multidrug Resistance Protein 4-Mediated Drug Efflux in the Kidney | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY |
| 2014 | A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy | SEIZURE-EUROPEAN JOURNAL OF EPILEPSY |
| 2013 | Increased systemic exposure of fimasartan, an angiotensin II receptor antagonist, by ketoconazole and rifampicin | JOURNAL OF CLINICAL PHARMACOLOGY |
| 2013 | Proximal Dominant Hereditary Motor and Sensory Neuropathy With Proximal Dominance Association With Mutation in the TRK-Fused Gene | JAMA NEUROLOGY |
| 2013 | Genetic Variations of ABCC2 Gene Associated with Adverse Drug Reactions to Valproic Acid in Korean Epileptic Patients
| Genomics & Informatics |
| 2013 | Combined effects of an antioxidant and caspase inhibitor on the reversal of hepatic fibrosis in rats | APOPTOSIS |
| 2013 | WNK4 inhibits plasma membrane targeting of NCC through regulation of syntaxin13 SNARE formation | CELLULAR SIGNALLING |
| 2013 | Association of genetic variation in chitotriosidase with atopy in Korean children | ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY |
| 2013 | Dynamic modulation of ANO1/TMEM16A HCO3− permeability by Ca2+/calmodulin
| PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA |
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