2015 | Multiple primary cancers involving lung cancer at a single tertiary hospital: Clinical features and prognosis | 장중현; 이진화; 류연주; 공경애 | Article |
2013 | MULTIPLE PRIMARY MALIGNANCIES IN PATIENTS WITH LUNG CANCER: CLINICAL FEATURES AND PROGNOSIS | 장중현; 이진화; 류연주; 이석정 | Meeting Abstract |
2009 | Multiple sclerosis and peripheral multifocal demyelinating neuropathies | 박기덕 | Meeting Abstract |
2008 | Multiple sclerosis and peripheral multifocal demyelinating neuropathies occurring in a same patient | 박기덕; 정지향 | Article |
2008 | Multiplex analysis of cytokines in the serum and cerebrospinal fluid of patients with Alzheimer's disease by color-coded bead technology | 최경규; 강상원; 최철희; 권종범; 정지향 | Article |
2010 | Multiplexed amino acid array utilizing bioluminescent escherichia coli auxotrophs | 최병옥 | Article |
2018 | Multitarget effects of Korean Red Ginseng in animal model of Parkinson's disease: antiapoptosis, antioxidant, antiinflammation, and maintenance of blood–brain barrier integrity | 오세관 | Article |
2016 | Musashi-2 (MSI2) supports TGF-beta signaling and inhibits claudins to promote non-small cell lung cancer (NSCLC) metastasis | 안영호 | Article |
2014 | Muscle involvement in Dent disease 2 | 이승주 | Article |
2006 | Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer | 정화순; 이경은 | Article |
2015 | MUTATION ANALYSIS OF JAK2, MPL, CALR, ASXL1, TET2, IDH1, IDH2, DNMT3A, AND SF3B1 IN MYELOPROLIFERATIVE NEOPLASM | 문영철 | Meeting Abstract |
2014 | Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy) | 조안나 | Article |
2005 | Mutational analysis of myelin protein zero gene in Korean families with Charcot-Marie-Tooth disease | 최병옥 | Meeting Abstract |
2005 | Mutational analysis of neurofilarnent light chain (NEFL) gene in Korean patients with Charcot-Marie-Tooth disease | 박기덕; 최병옥 | Meeting Abstract |
2010 | Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases | 최병옥 | Article |
2007 | Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (CMTX5) | 최병옥 | Article |
2013 | Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease | 구혜수; 유정현; 최병옥 | Article |
2009 | Mutations of E3 Ubiquitin Ligase Cbl Family Members Constitute a Novel Common Pathogenic Lesion in Myeloid Malignancies | 허정원 | Article |
2007 | Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families | 최병옥 | Article |
2010 | Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns | 강덕희 | Article |