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Issue DateTitleJournal Title
201115-deoxy-D12,14-prostaglandin J2 suppresses RANTES expression by inhibiting NADPH oxidase activation in Helicobacter pylori-infected gastric epithelial cells JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
200915-Deoxy-delta 12, 14,-prostaglandin J2 suppresses nuclear factor-kappaB-mediated apoptosis of Helicobacter pylori-infected gastric epithelial cellsANNALS OF THE NEW YORK ACADEMY OF SCIENCES
201017-베타 에스트라디올이 OLETF 쥐의 지방세포 Lipin-1 발현에 미치는 영향 Journal of Korea Society of Endocrinology (대한내분비학회지)
2015[(18)F]FPEB and [(18)F]FDEGPECO comparative study of mGlu5 quantification in rodent brainAPPLIED RADIATION AND ISOTOPES
20032nd International Symposium: Frontiers in Pancreatic Research—From Basics to Clinic and Exocrine Glands, Japan–KoreaPANCREAS
2010A case of combined hepatocellular-cholangiocarcinoma with favorable response to systemic chemotherapy CANCER RESEARCH AND TREATMENT
2017A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBDGUT
2022A database of 5305 healthy Korean individuals reveals genetic and clinical implications for an East Asian population EXPERIMENTAL AND MOLECULAR MEDICINE
2012A facile approach for the delivery of inorganic nanoparticles into the brain by passing through the blood-brain barrier (BBB).CHEMICAL COMMUNICATIONS
2016A genetic variant in GLP1R is associated with response to DPP-4 inhibitors in patients with type 2 diabetes MEDICINE
2003A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases HUMAN MOLECULAR GENETICS
2011A low-risk ZnT-8 allele (W325) for post-transplantation diabetes mellitus is protective against cyclosporin A-induced impairment of insulin secretionPHARMACOGENOMICS JOURNAL
2002A molecular mechanism for aberrant CFTR-dependent HCO3- transport in cystic fibrosis EMBO JOURNAL
2018A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes CELL REPORTS
2014A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsySEIZURE-EUROPEAN JOURNAL OF EPILEPSY
2010A nonsynonymous variation in MRP2/ABCC2 is associated with neurological adverse drug reactions of carbamazepine in patients with epilepsy.PHARMACOGENETICS AND GENOMICS
2015A Novel BEST1 Mutation in Autosomal Recessive BestrophinopathyINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
2019A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunctionEUROPEAN JOURNAL OF MEDICAL GENETICS
2000A novel effect of rebamipide: generation of Ca oscillations through activation of CCk1 receptors in rat pancreatic acinar cellsEuropean Journal of Pharmacology
2018A novel HIF1AN substrate KANK3 plays a tumor-suppressive role in hepatocellular carcinomaCELL BIOLOGY INTERNATIONAL

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