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Showing results 22361 to 22380 of 57409

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Issue DateTitleYonsei Author(s)Type
2008Mutation in the transcriptional regulator PhoP contributes to avirulence of Mycobacterium tuberculosis H37Ra strain. 곽정연, 전보영, 조상래Article
2020Mutation landscape of germline and somatic BRCA1/2 in patients with high-grade serous ovarian cancer 김상운, 김성훈, 김영태, 김혜민, 남은지, 어경진, 이정윤Article
2013Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype지헌영Article
2016Mutation profiling of 19 candidate genes in acute myeloid leukemia suggests significance of DNMT3A mutations 이승태Article
2012Mutation spectrum of NIPBL gene in Korean patients with Cornelia de Lange syndrome 왕지영Thesis
2005Mutation spectrum of the APC gene in 83 Korean FAP families김남규Article
2013Mutational Analysis of EYA1, SIX1 and SIX5 Genes and Strategies for Management of Hearing Loss in Patients with BOR/BO Syndrome 이원상, 최재영Article
2015Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance 조병철Article
2005Mutational spectrum of NF1 gene in Korean patients with neurofibromatosis type 1 이철호Thesis
2008Mutations in both KRAS and BRAF may contribute to the methylator phenotype in colon cancer 신성관Article
2017Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease 지헌영Article
2014Mutations in EMP2 cause childhood-onset nephrotic syndrome 지헌영Article
2010Mutations in extensively drug-resistant Mycobacterium tuberculosis that do not code for known drug-resistance mechanisms 조상래Article
2011Mutations in isocitrate dehydrogenase isoforms 1 and 2 are rare events in primary central nervous system and non-central nervous system diffuse large B cell lymphoma김세훈Article
2017Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly 지헌영Article
2019Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome지헌영Article
2017Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis지헌영Article
2018Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome 지헌영Article
2008Mutations in NALP12 cause hereditary periodic fever syndromes 유제욱Article
2016Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome. 지헌영Article

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