Browsing by Yonsei Author : Lee, Ji Hyun

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Name:
Lee, Ji Hyun [이지현]
Department :
College of Dentistry (치과대학) - Dept. of Oral Biology (구강생물학교실)

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Showing results 1 to 46 of 46

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Issue DateTitleJournal Title
2024Novel Clinical Anatomical Consideration of the Superficial and Deep Layers of the Deep Temporal FasciaPLASTIC AND RECONSTRUCTIVE SURGERY
2023Sonoanatomy and an ultrasound scanning protocol of the intramuscular innervation pattern of the infraspinatus muscleREGIONAL ANESTHESIA AND PAIN MEDICINE
2023Evaluating intramuscular neural distribution in the cricopharyngeus muscle for injecting botulinum toxinAURIS NASUS LARYNX
2022Novel Anatomical Proposal for Botulinum Neurotoxin Injection Targeting Lateral Canthal Rhytids TOXINS
2022The Superficial Temporal Artery and Zygomatico-Orbital Artery: Superficial Arterial Distribution of the Anterior Temple Area BIOMED RESEARCH INTERNATIONAL
2020Extracellular vesicles derived from macrophages display glycyl-tRNA synthetase 1 and exhibit anti-cancer activity JOURNAL OF EXTRACELLULAR VESICLES
2016Ecological changes in oral microcosm biofilm during maturation JOURNAL OF BIOMEDICAL OPTICS
2016First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy JOURNAL OF CLINICAL NEUROLOGY
2016Clinical assessment of oral malodor using autofluorescence of tongue coatingPHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY
2015Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1NEUROMUSCULAR DISORDERS
2015Genome-wide association study of recalcitrant atopic dermatitis in Korean childrenJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
2015Genetic association between VEGF polymorphisms and BRONJ in the Korean populationORAL DISEASES
2015Clinical features of familial hypercholesterolemia in Korea: Predictors of pathogenic mutations and coronary artery disease - A study supported by the Korean Society of Lipidology and AtherosclerosisATHEROSCLEROSIS
2015Evaluation of polygenic cause in Korean patients with familial hypercholesterolemia - A study supported by Korean Society of Lipidology and AtherosclerosisATHEROSCLEROSIS
2015GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsyEPILEPSY RESEARCH
2015Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis PLOS ONE
2015Targeted next-generation sequencing for the genetic diagnosis of dysferlinopathyNEUROMUSCULAR DISORDERS
2015Genetic testing of Korean familial hypercholesterolemia using whole-exome sequencing PLOS ONE
2015microDuMIP: target-enrichment technique for microarray-based duplex molecular inversion probes NUCLEIC ACIDS RESEARCH
2015Phase II clinical and exploratory biomarker study of dacomitinib in patients with recurrent and/or metastatic squamous cell carcinoma of head and neckCLINICAL CANCER RESEARCH
2014Perturbation of NCOA6 Leads to Dilated CardiomyopathyCELL REPORTS
2014Identification of somatic mutations in EGFR/KRAS/ALK-negative lung adenocarcinoma in never-smokers GENOME MEDICINE
2014Whole-Genome Analysis in Korean Patients with Autoimmune Myasthenia Gravis YONSEI MEDICAL JOURNAL
2014A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsySEIZURE-EUROPEAN JOURNAL OF EPILEPSY
2013Proximal Dominant Hereditary Motor and Sensory Neuropathy With Proximal Dominance Association With Mutation in the TRK-Fused GeneJAMA NEUROLOGY
2013Genetic Variations of ABCC2 Gene Associated with Adverse Drug Reactions to Valproic Acid in Korean Epileptic Patients Genomics & Informatics
2013Association between CDH13 Variants and Cardiometabolic and Vascular Phenotypes in a Korean Population YONSEI MEDICAL JOURNAL
2013Pharmacogenetic determinants associated with sunitinib-induced toxicity and ethnic difference in Korean metastatic renal cell carcinoma patientsCANCER CHEMOTHERAPY AND PHARMACOLOGY
2013Pharmacogenomic Assessment of Outcomes of Pemetrexed-Treated Patients with Adenocarcinoma of the Lung YONSEI MEDICAL JOURNAL
2013Association of genetic variation in chitotriosidase with atopy in Korean childrenANNALS OF ALLERGY ASTHMA & IMMUNOLOGY
2013Fibroblast Growth Factor Receptor 1 Gene Amplification Is Associated With Poor Survival and Cigarette Smoking Dosage in Patients With Resected Squamous Cell Lung CancerJOURNAL OF CLINICAL ONCOLOGY
2012EGFR polymorphism as a predictor of clinical outcome in advanced lung cancer patients treated with EGFR-TKI YONSEI MEDICAL JOURNAL
2012Activation of IL-6R/JAK1/STAT3 signaling induces de novo resistance to irreversible EGFR inhibitors in non-small cell lung cancer with T790M resistance mutationMOLECULAR CANCER THERAPEUTICS
2012TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's diseaseBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
2011A synonymous variation in protease-activated receptor-2 is associated with atopy in Korean childrenJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
2010Association between cystic fibrosis transmembrane conductance regulator gene mutations and susceptibility for childhood asthma in Korea YONSEI MEDICAL JOURNAL
2010MRP1 polymorphisms associated with citalopram response in patients with major depressionJOURNAL OF CLINICAL PSYCHOPHARMACOLOGY
2010A nonsynonymous variation in MRP2/ABCC2 is associated with neurological adverse drug reactions of carbamazepine in patients with epilepsy.PHARMACOGENETICS AND GENOMICS
2010Selective inhibition of MDR1 (ABCB1) by HM30181 increases oral bioavailability and therapeutic efficacy of paclitaxel.EUROPEAN JOURNAL OF PHARMACOLOGY
2010The L441P mutation of cystic fibrosis transmembrane conductance regulator and its molecular pathogenic mechanisms in a Korean patient with cystic fibrosis JOURNAL OF KOREAN MEDICAL SCIENCE
2009Genetic variation in the promoter region of chitinase 3-like 1 is associated with atopy.AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
2007MRP2 haplotypes confer differential susceptibility to toxic liver injuryPHARMACOGENETICS AND GENOMICS
2007Dynamic regulation of cystic fibrosis transmembrane conductance regulator by competitive interactions of molecular adaptors JOURNAL OF BIOLOGICAL CHEMISTRY
2005Gene SNPs and mutations in clinical genetic testing: Haplotype-based testing and analysisMUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
2004Inhibitory regulation of cystic fibrosis transmembrane conductance regulator anion-transporting activities by Shank2 JOURNAL OF BIOLOGICAL CHEMISTRY
2003A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases HUMAN MOLECULAR GENETICS
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