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