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YUHSpace1. College of Medicine (의과대학)Dept. of Pharmacology (약리학교실)1. Journal Papers

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Issue DateTitleJournal Title
2017Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population SCIENTIFIC REPORTS
2017A randomized controlled trial of various MTA materials for partial pulpotomy in permanent teethJOURNAL OF DENTISTRY
2017Adult-Onset Vitelliform Macular Dystrophy caused by BEST1 p.Ile38Ser Mutation is a Mild Form of Best Vitelliform Macular Dystrophy SCIENTIFIC REPORTS
2017Experience and pharmacokinetics of Levetiracetam in Korean neonates with neonatal seizures Korean Journal of Pediatrics
2017UDP-Induced Phagocytosis and ATP-Stimulated Chemotactic Migration Are Impaired in STIM1-/- Microglia In Vitro and In Vivo MEDIATORS OF INFLAMMATION
2017Relationships between Psychosocial Difficulties and Oxidative Stress Biomarkers in Women Subject to Intimate Partner ViolenceHEALTH & SOCIAL WORK
2017Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency JOURNAL OF CLINICAL INVESTIGATION
2017Biological efficacy of two mineral trioxide aggregate (MTA)-based materials in a canine model of pulpotomy DENTAL MATERIALS JOURNAL
2017Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical DysplasiaAMERICAN JOURNAL OF HUMAN GENETICS
2017Optimizing reproducibility of operant testing through reinforcer standardization: identification of key nutritional constituents determining reward strength in touchscreens MOLECULAR BRAIN
2017Hippocampus-Dependent Goal Localization by Head-Fixed Mice in Virtual Reality ENEURO
2017Adopting automated image analysis tool for fibrin network: Can we obtain clot properties for practical application?INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY
2017소아에서 비전형적인 임상양상을 보인 스피츠모반 1예Korean Journal of Dermatology (대한피부과학회지)
2017A novel missense mutation in NR0B1 causes delayed-onset primary adrenal insufficiency in adultsCLINICAL GENETICS
2017Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome JOURNAL OF CLINICAL INVESTIGATION
2017Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease NATURE GENETICS
2017Oncogenic BRAF fusions in mucosal melanomas activate the MAPK pathway and are sensitive to MEK/PI3K inhibition or MEK/CDK4/6 inhibitionONCOGENE
2017A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBDGUT
2017Green Teeth Associated Hyperbilirubinemia in Primary Dentition Journal of the Korean Academy of Pediatric Dentistry (대한소아치과학회지)
2017Cystic kidneys in fetal Walker-Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literatureAMERICAN JOURNAL OF MEDICAL GENETICS PART A
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