2017 | A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD | GUT |
2003 | A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases
| HUMAN MOLECULAR GENETICS |
2002 | A molecular mechanism for aberrant CFTR-dependent HCO3- transport in cystic fibrosis
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2014 | A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy | SEIZURE-EUROPEAN JOURNAL OF EPILEPSY |
2010 | A nonsynonymous variation in MRP2/ABCC2 is associated with neurological adverse drug reactions of carbamazepine in patients with epilepsy. | PHARMACOGENETICS AND GENOMICS |
2015 | A Novel BEST1 Mutation in Autosomal Recessive Bestrophinopathy | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE |
2000 | A novel effect of rebamipide: generation of Ca oscillations through activation of CCk1 receptors in rat pancreatic acinar cells | European Journal of Pharmacology |
2021 | A pilot study to investigate the utility of NAT2 genotype-guided isoniazid monotherapy regimens in NAT2 slow acetylators | PHARMACOGENETICS AND GENOMICS |
2002 | A protein sequence that can encode native structure by disfavoring alternate conformations | NATURE STRUCTURAL BIOLOGY |
2019 | A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators | HUMAN MUTATION |
2011 | A small molecule that binds to an ATPase domain of Hsc70 promotes membrane trafficking of mutant cystic fibrosis transmembrane conductance regulator. | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY |
2011 | A synonymous variation in protease-activated receptor-2 is associated with atopy in Korean children | JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY |
2001 | Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis
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2020 | ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY |
2017 | Adult-Onset Vitelliform Macular Dystrophy caused by BEST1 p.Ile38Ser Mutation is a Mild Form of Best Vitelliform Macular Dystrophy
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2022 | Amelioration of SARS-CoV-2 infection by ANO6 phospholipid scramblase inhibition
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2015 | Analysis of conventional and unconventional trafficking of CFTR and other membrane proteins | Methods in Molecular Biology (Clifton, N.J.) |
2017 | ANO9/TMEM16J promotes tumourigenesis via EGFR and is a novel therapeutic target for pancreatic cancer | BRITISH JOURNAL OF CANCER |
2010 | Association between cystic fibrosis transmembrane conductance regulator gene mutations and susceptibility for childhood asthma in Korea
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2011 | Association of a synonymous GAT3 polymorphism with antiepileptic drug pharmacoresistance | JOURNAL OF HUMAN GENETICS |
2010 | Association of ABCB1 polymorphisms with the efficacy of ondansetron for postoperative nausea and vomiting. | ANAESTHESIA |
2013 | Association of genetic variation in chitotriosidase with atopy in Korean children | ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY |
2012 | Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function | NATURE |
2022 | Autophagy-Related Pathways in Vesicular Unconventional Protein Secretion
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2005 | Base Treatment Corrects Defects Due to Misfolding of Mutant Cystic Fibrosis Transmembrane Conductance Regulator | GASTROENTEROLOGY |
2016 | Benefit of Adjuvant Chemotherapy After Curative Resection of Lung Metastasis in Colorectal Cancer | ANNALS OF SURGICAL ONCOLOGY |
2015 | Benzopyrimido-pyrrolo-oxazine-dione (R)-BPO-27 Inhibits CFTR Chloride Channel Gating by Competition with ATP | MOLECULAR PHARMACOLOGY |
2010 | BetaPix up-regulates Na+/H+ exchanger 3 through a Shank2-mediated protein-protein interaction
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2020 | Bicarbonate permeation through anion channels: its role in health and disease | PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY |
2003 | Ca2+ Activates Cystic Fibrosis Transmembrane Conductance Regulator- and Cl−-dependent HCOFormula Transport in Pancreatic Duct Cells
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2009 | Chloride intracellular channel 1 regulates osteoblast differentiation | BONE |
2012 | Cholesterol modulates cell signaling and protein networking by specifically interacting with PDZ domain-containing scaffold proteins
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2017 | Chronological Change of Right Ventricle by Chronic Intermittent Hypoxia in Mice | SLEEP |
2016 | Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations
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2013 | Combined effects of an antioxidant and caspase inhibitor on the reversal of hepatic fibrosis in rats | APOPTOSIS |
2017 | Comparison of clinical outcomes between wavefront-optimized versus corneal wavefront-guided transepithelial photorefractive keratectomy for myopic astigmatism | JOURNAL OF CATARACT AND REFRACTIVE SURGERY |
1999 | Cystic fibrosis transmembrane conductance regulator regulates luminal Cl-/HCO3- exchange in mouse submandibular and pancreatic ducts
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2022 | Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation
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2020 | Digenic Inheritance of Mutations in EPHA2 and SLC26A4 in Pendred Syndrome
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2020 | Distinct Mechanisms of Over-Representation of Landmarks and Rewards in the Hippocampus
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2020 | DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model
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2015 | Does calmodulin regulate the bicarbonate permeability of ANO1/TMEM16A or not?
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1999 | Dynamic association of proteasomal machinery with the centrosome
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2013 | Dynamic modulation of ANO1/TMEM16A HCO3− permeability by Ca2+/calmodulin
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2010 | Dynamic regulation of CFTR bicarbonate permeability by [Cl-]i and its role in pancreatic bicarbonate secretion. | GASTROENTEROLOGY |
2007 | Dynamic regulation of cystic fibrosis transmembrane conductance regulator by competitive interactions of molecular adaptors
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2016 | Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice
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2007 | Effect of Slc26a6 deletion on apical Cl−/HCO3− exchanger activity and cAMP-stimulated bicarbonate secretion in pancreatic duct
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2009 | Effects of KR-33028, a novel Na+/H+ exchanger-1 inhibitor, on glutamate-induced neuronal cell death and ischemia-induced cerebral infarct | BRAIN RESEARCH |
2010 | Effects of SLCO1B1 and ABCB1 genotypes on the pharmacokinetics of atorvastatin and 2-hydroxyatorvastatin in healthy Korean subjects | INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS |
2017 | Enhancing inhibitory synaptic function reverses spatial memory deficits in Shank2 mutant mice | NEUROPHARMACOLOGY |
1996 | Evaluation of anti-influenza effects of camostat in mice infected with non-adapted human influenza viruses | ARCHIVES OF VIROLOGY |
2005 | Expression of Na+/H+ exchanger isoforms in normal human nasal epithelial cells and functional activity of Na+/H+ exchanger 1 in intracellular pH regulation | ACTA OTO-LARYNGOLOGICA |
2019 | Functional Characterization of Pharmcogenetic Variants of Human Cytochrome P450 2C9 in Korean Populations
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2005 | Gene SNPs and mutations in clinical genetic testing: Haplotype-based testing and analysis | MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS |
2016 | Generation of ΔF508-CFTR T84 cell lines by CRISPR/Cas9-mediated genome editing | BIOTECHNOLOGY LETTERS |
2015 | Genetic testing of Korean familial hypercholesterolemia using whole-exome sequencing
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2009 | Genetic variation in the promoter region of chitinase 3-like 1 is associated with atopy. | AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE |
2013 | Genetic Variations of ABCC2 Gene Associated with Adverse Drug Reactions to Valproic Acid in Korean Epileptic Patients
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2024 | Genome-wide association analysis reveals the associations of NPHP4, TYW1-AUTS2 and SEMA6D for Behçet's disease and HLA-B*46:01 for its intestinal involvement | DIGESTIVE AND LIVER DISEASE |