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

Agoraphobia

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

神刊

Orchiectomy

anagen

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

Substance

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

刪減

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

cutlery

Hallmark