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J-GLOBAL ID：201902219502761455   Reference number：19A2148574

慢性閉塞性肺疾患におけるCFTR機能異常機構の解明

Author (1)： OKIYONEDA TSUKASA (関西学院大 理工)
Material： 医科学応用研究財団研究報告(CD-ROM)  (Research Papers of the Suzuken Memorial Foundation (CD-ROM))
Volume： 35  Page： 169-174  Publication year： Feb. 2018 
JST Material Number： L0786B  ISSN： 2185-2561  CODEN： IOKHEP  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： JAPANESE (JA)

Thesaurus term： *chronic obstructive pulmonary disease ,...
Semi thesaurus term： Cystic Fibrosis Transmembrane Conductance Regulator ,...

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JST classification (1)： Basic medicine on respiratory system  (GI01020H)

Substance index (1)： Dynasore

Reference (23)：

• M. Osthoff, C. Jenkins, J. Leuppi:Chronic obstructive pulmonary disease--a treatable disease. Swiss Med Wkly. 143:w13777, 2013.
• M. Tzetis, A. Efthymiadou, S. Doudounakis, E. Kanavakis:Qualitative and quantitative analysis of mRNA associated with four putative splicing mutations (621+3A-->G, 2751+2T-->A, 296+1G-->C, 1717-9T-->C-D565G) and one nonsense mutation(E822X) in the CFTR gene. Hum Genet. 109:592-601, 2001.
• A. Divac et al:High frequency of the R75Q CFTR variation in patients with chronic obstructive pulmonary disease. J Cyst Fibros. 3:189-191, 2004.
• M. Stankovic et al:The CFTR M470V gene variant as a potential modifier of COPD severity: study of Serbian population. Genet Test. 12:357-362, 2008.
• M. T. Dransfield et al:Acquired cystic fibrosis transmembrane conductance regulator dysfunction in the lower airways in COPD. Chest. 144:498-506, 2013.

Terms in the title (3)： 慢性閉塞性肺疾患 ,  CFTR ,  機能異常