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Showing results 21501 to 21520 of 73751

Issue DateTitleAuthor(s)Type
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
2010Mutations in SOHLH1 gene associate with nonobstructive azoospermia권영주Article
2013Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease구혜수; 유정현; 최병옥Article
2011Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiency여성희Article
2009Mutations of E3 Ubiquitin Ligase Cbl Family Members Constitute a Novel Common Pathogenic Lesion in Myeloid Malignancies허정원Article
2007Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families최병옥Article
2010Mutations of the GLA gene in Korean patients with Fabry disease and frequency of the E66Q allele as a functional variant in Korean newborns강덕희Article
2013Mutations of the TATA-binding protein confer enhanced tolerance to ethanol and hyperosmotic stress in Saccharomyces cerevisiae권혜지Master's Thesis
2013Mutations of the TATA-binding protein confer enhanced tolerance to hyperosmotic stress in Saccharomyces cerevisiae최원자Article

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