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Titlebook: Cystic Fibrosis; Diagnosis and Protoc Margarida D. Amaral,Karl Kunzelmann Book 2011 Springer Science+Business Media, LLC 2011 CF.CFTR expre

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書目名稱Cystic Fibrosis
副標題Diagnosis and Protoc
編輯Margarida D. Amaral,Karl Kunzelmann
視頻videohttp://file.papertrans.cn/243/242592/242592.mp4
概述Features cutting-edge protocols from the highly supportive CF scientific community.Contains expert tips and key implementation advice.Focuses on Cystic fibrosis transmembrane conductance regulator def
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Cystic Fibrosis; Diagnosis and Protoc Margarida D. Amaral,Karl Kunzelmann Book 2011 Springer Science+Business Media, LLC 2011 CF.CFTR expre
描述.Despite the many milestones in cystic fibrosis (CF) research, progress towards curing the disease has been slow, and it is increasingly difficult to grasp and use the already wide and still growing range of diverse methods currently employed to study CF so as to understand it in its multidisciplinary nature.? .Cystic Fibrosis: Diagnosis and Protocols. aims to provide the CF research community and related researchers with a very wide range of high-quality experimental tools, as an easy way to grasp and use classical and novel methods applied to cystic fibrosis.? .Volume I: Approaches to Study and Correct CFTR Defects. focuses on the cystic fibrosis transmembrane conductance regulator (CFTR)?and its expression, biogenesis, structure, and function in terms of the defects causing CF.? Written in the highly successful .Methods in Molecular Biology.? series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls..?.Comprehensive and practical, .Cystic Fibrosis: Diagnosis and Protocols. will provide readers with optimal
出版日期Book 2011
關(guān)鍵詞CF; CFTR expression; Human clinical trials; Protein biogenesis and folding; RNA methods; Structure and fu
版次1
doihttps://doi.org/10.1007/978-1-61779-117-8
isbn_softcover978-1-4939-5787-3
isbn_ebook978-1-61779-117-8Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC 2011
The information of publication is updating

書目名稱Cystic Fibrosis影響因子(影響力)




書目名稱Cystic Fibrosis影響因子(影響力)學(xué)科排名




書目名稱Cystic Fibrosis網(wǎng)絡(luò)公開度




書目名稱Cystic Fibrosis網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Cystic Fibrosis被引頻次




書目名稱Cystic Fibrosis被引頻次學(xué)科排名




書目名稱Cystic Fibrosis年度引用




書目名稱Cystic Fibrosis年度引用學(xué)科排名




書目名稱Cystic Fibrosis讀者反饋




書目名稱Cystic Fibrosis讀者反饋學(xué)科排名




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In Vitro Methods for CFTR Biogenesisgth CFTR expression can be markedly increased using mRNA lacking a 5.-cap analog (G(5.)ppp(5.)G), whereas the reverse usually holds for smaller proteins and individual CFTR domains. In the context of the full-length mRNA, translation was further stimulated by the presence of a long 3.-UTR. The secon
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Book 2011ons to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls..?.Comprehensive and practical, .Cystic Fibrosis: Diagnosis and Protocols. will provide readers with optimal
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1064-3745 p, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls..?.Comprehensive and practical, .Cystic Fibrosis: Diagnosis and Protocols. will provide readers with optimal978-1-4939-5787-3978-1-61779-117-8Series ISSN 1064-3745 Series E-ISSN 1940-6029
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