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Issue DateTitleJournal Title
2016Diagnosis of Severe Protein C Deficiency Confirmed by Presence of Rare PROC Gene Mutation Neonatal Medicine
2008Differential gene expression profiles of metastases in paired primary and metastatic colorectal carcinomasONCOLOGY
2010Effect of severe neonatal morbidities on long term outcome in extremely low birthweight infants Korean Journal of Pediatrics
2001Expression of genes involved in mammalian meiosis during the transition from egg to embryoMOLECULAR REPRODUCTION AND DEVELOPMENT
2007Frequent inactivation of SPARC by promoter hypermethylation in colon cancersINTERNATIONAL JOURNAL OF CANCER
2011Gene expression changes in patient-matched gastric normal mucosa, adenomas, and carcinomasEXPERIMENTAL AND MOLECULAR PATHOLOGY
2012Genetic and epileptic features in Rett syndrome YONSEI MEDICAL JOURNAL
2014Germline mutation of Glu70Lys is highly frequent in Korean patients with von Hippel–Lindau (VHL) diseaseJOURNAL OF HUMAN GENETICS
2016Identification of disease comorbidity through hidden molecular mechanisms SCIENTIFIC REPORTS
2014Isolated cerebellar variant of adrenoleukodystrophy with a de novo adenosine triphosphate-binding cassette D1 (ABCD1) gene mutation. YONSEI MEDICAL JOURNAL
2008Macrophage migration inhibitory factor may be used as an early diagnostic marker in colorectal carcinomas AMERICAN JOURNAL OF CLINICAL PATHOLOGY
2009MedRefSNP: a database of medically investigated SNPsHUMAN MUTATION
2016Mucocutaneous Telangiectasia as a Diagnostic Clue of Hereditary Hemorrhagic Telangiectasia: An Activin Receptor-Like Kinase-1 Mutation in a Korean Patient ANNALS OF DERMATOLOGY
2011Neural Stem Cells: Properties and Therapeutic Potentials for Neonatal Hypoxic-Ischemic Brain InjuryVascular Neurology
2014Novel mutations of KIT gene in two Korean patients: Variegated shades of phenotypes in tyrosine kinase 1 domainJOURNAL OF DERMATOLOGICAL SCIENCE
2004Proteomic analysis distinguishes basaloid carcinoma as a distinct subtype of nonsmall cell lung carcinomaPROTEOMICS
2012The first case of familial Mediterranean fever associated with renal amyloidosis in Korea YONSEI MEDICAL JOURNAL
2016Unravelling the mechanism of action of enzyme replacement therapy in Fabry diseaseJOURNAL OF HUMAN GENETICS
2016Variations in plasma and urinary lipids in response to enzyme replacement therapy for Fabry disease patients by nanoflow UPLC-ESI-MS/MS.ANALYTICAL AND BIOANALYTICAL CHEMISTRY
2013신생아 저산소성 허혈성 뇌손상에서 신경줄기세포의 치료적 적용 Neonatal Medicine
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