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

Agoraphobia

书目名称Cystic Fibrosis影响因子(影响力)




书目名称Cystic Fibrosis影响因子(影响力)学科排名




书目名称Cystic Fibrosis网络公开度




书目名称Cystic Fibrosis网络公开度学科排名




书目名称Cystic Fibrosis被引频次




书目名称Cystic Fibrosis被引频次学科排名




书目名称Cystic Fibrosis年度引用




书目名称Cystic Fibrosis年度引用学科排名




书目名称Cystic Fibrosis读者反馈




书目名称Cystic Fibrosis读者反馈学科排名

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Book 2011the 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 working tools to address pressing questi

Nmda-Receptor

Introduction to Section II: Omics in the Biology of Cystic Fibrosisand CF pathophysiology, a new era of technologies and methodologies focused on systems-level approaches to analysis of cell and tissue function has emerged. These technologies focus our understanding on the environment supporting protein function (referred to genomics) and the protein composition of

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Substance

Introduction to Section I: Overview of Approaches to Study Cystic Fibrosis Pathophysiologyological changes occurring in CF lung disease with the mutation of a chloride channel is ongoing. The failure of innate lung defense in CF, and the subsequent cyclical microbial colonization of airways, explains the gross anatomical changes that occur in CF pathophysiology. However, ongoing research

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Imaging CFTR Protein Localization in Cultured Cells and Tissuescommonly used to assess the subcellular localization and relative abundance of CFTR. Visualization of heterologously overexpressed CFTR is typically unproblematic and straightforward, whereas detection of small quantities of endogenous CFTR in tissues can be challenging and requires highly specific

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