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Showing results 8581 to 8600 of 13855

Pub YearTitleAuthor(s)
2018Multiple Wavelength Optical Coherence Tomography Assessments for Enhanced Ex Vivo Intra-Cochlear Microstructural Visualization장정훈
2016Multisite Evaluation of a Data Quality Tool for Patient-Level Clinical Data Sets박래웅
2014Multistage genome-wide association meta-analyses identified two new loci for bone mineral density.조남한
2023Multivalent Carbohydrate Nanocomposites for Tumor Microenvironment Remodeling to Enhance Antitumor Immunity김유선
2020Multivariate analyses of MRI findings for predicting osteomyelitis of the foot in diabetic patients곽규성, 박성훈, 박영욱
2021Multivariate analysis of early surgical management factors affecting posttraumatic penoscrotal avulsion injury: a level I trauma center study김민지, 박동하, 이일재
2001Murine model of atopic dermatitis associated with food hypersensitivity.이수영
2005Murine model of buckwheat allergy by intragastric sensitization with fresh buckwheat flour extract.이수영, 장영주
2014Muscle involvement in Dent disease 2.박세진
2012Mutagenesis by imprecise excision of the piggyBac transposon in Drosophila melanogaster김송희
2004Mutant p53 protein in the serum of patients with cervical carcinoma: correlation with the level of serum epidermal growth factor receptor and prognostic significance.최진혁
2000Mutation analysis of Korean patients with citrullinemia.한시훈
2005Mutation analysis of the MCM gene in Korean patients with MMA.김성환, 박준은, 정조원, 황진순
2022Mutation spectrum and genotype–phenotype correlations in 157 Korean CADASIL patients: a multicenter study박서진
2013Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.김현주, 손영배, 정선용
2012Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism김현주, 정선용
2018Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinics장정훈, 정연훈
2017Mutations acquired by hepatocellular carcinoma recurrence give rise to an aggressive phenotype권소미, 왕희정, 우현구
2014Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy김옥화
2020Mutations in the SARS-CoV-2 spike RBD are responsible for stronger ACE2 binding and poor anti-SARS-CoV mAbs cross-neutralizationSHAH, MASAUD, 우현구

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