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Showing results 681 to 700 of 17605

Pub YearTitleAuthor(s)
2014A novel delivery platform for therapeutic peptides.박준성
2014A novel designed screw with enhanced stability introduces new way of intermaxillary fixation.정규림
1999A novel disintegrin salmosin inhibits tumor angiogenesis.이영돈
2018A Novel Eosinophilia Diagnostics Using Label‐free Impedimetric Aptasensor for Soluble Interleukin‐5 Receptor Alpha박해심
1998A novel ets-related transcription factor, ERT/ESX/ESE-1, regulates expression of the transforming growth factor-beta type II receptor.함기백
2017A novel flexible drill device enabling arthroscopic transosseous repair of Bankart lesions원예연
2020A Novel Fracture Prediction Model Using Machine Learning in a Community-Based Cohort조남한
2004A Novel Gene Therapy for Uterine Cervical Cancer and Renal Cell Carcinoma Using MN/CA9 Promoter-based Replication Competent Adenovirus안미원
2000A novel germ line juxtamembrane Met mutation in human gastric cancer.이재호, 조혜성, 한상욱
2022A novel global ischemia-reperfusion rat model with asymmetric brain damage simulating post-cardiac arrest brain injury김민, 박소영, 홍지만
2010A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome.김옥화, 김현주, 정선용
2007A Novel Index of Microcirculatory Resistance for Invasively Assessing Myocardial Viability after Primary Angioplasty for Treating Acute Myocardial Infarction: Comparison with FDG-PET Imaging강수진, 신준한, 우성일, 윤명호, 임홍석, 최병주, 최소연, 최운정, 탁승제, 황교승, 황정원
2015A novel isoform of met receptor tyrosine kinase blocks hepatocyte growth factor/Met signaling and stimulates skeletal muscle cell differentiation.김철호, 이광, 이복순, 이재호, 조혜성
2022A Novel KCNA1 Variant Manifesting as Persistent Limb Myokymia Without Episodic Ataxia손성연, 주인수
2013A novel MLL2 gene mutation in a Korean patient with Kabuki syndrome손영배
2008A Novel Mouse Model of Asthma Induced by Cockroach신유섭
2000A novel mutation in the beta-hexosaminidase beta-subunit gene in a 14-month-old Korean boy with Sandhoff disease: first reported Korean case.한시훈
2014A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation.정주용
2024A novel nerve block technique for nail surgery최지웅
2004A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness.주인수, 허균

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