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Showing results 21421 to 21440 of 73652

Issue DateTitleAuthor(s)Type
2019Muscle Talk Online and Impression Formation Based on Body Type: Comparisons Between Asian American and Caucasian American Males이혜은Article
2020Muscle-based Real-time Facial Animation using Shell Elements and Force Decomposition김정민Master's Thesis
2013Musculoskeletal problems need more attention in deep brain stimulation for parkinson's disease윤지영Article
2015Music analysis as poetry조현리Article
2012Music in Words이현지Master's Thesis
2017Music perception training for pediatric cochlear implant recipients ages 3 to 5 years: A pilot study김수지Article
2017Mutable Properties of Nonheme Iron(III)-Iodosylarene Complexes Result in the Elusive Multiple-Oxidant Mechanism남원우Article
2006Mutagenesis and modeling of the peroxiredoxin (Prx) complex with the NMR structure of ATP-bound human sulfiredoxin implicate aspartate 187 of Prx I as the catalytic residue in ATP hydrolysis이서구; 정우진Article
1997Mutagenesis를 이용한 무스카린성 아세틸콜린 수용체 subtype Hm2와 Hm3의 길항제 선택성에 관여하는 부위규명에 대한 연구우예봉Master's Thesis
2011Mutant generation for embedded systems using kernel-based software and hardware fault simulation최병주Article
2006Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer정화순; 이경은Article
2015MUTATION ANALYSIS OF JAK2, MPL, CALR, ASXL1, TET2, IDH1, IDH2, DNMT3A, AND SF3B1 IN MYELOPROLIFERATIVE NEOPLASM문영철Meeting Abstract
2014Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy)조안나Article
2005Mutational analysis of myelin protein zero gene in Korean families with Charcot-Marie-Tooth disease최병옥Meeting Abstract
2005Mutational analysis of neurofilarnent light chain (NEFL) gene in Korean patients with Charcot-Marie-Tooth disease박기덕; 최병옥Meeting Abstract
2004Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients.최경규; 최병옥Article
2010Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases최병옥Article
2013Mutational biosynthesis of a FK506 analogue containing a non-natural starter unit윤여준; 모상준Article
2015Mutations Decouple Proton Transfer from Phosphate Cleavage in the dUTPase Catalytic ReactionPankaz Kumar SharmaArticle
2007Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (CMTX5)최병옥Article

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