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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 questiNmda-Receptor 发表于 2025-3-22 12:27:51
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 ofSubstance 发表于 2025-3-22 15:52:17
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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删减 发表于 2025-3-22 23:05:49
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 specificcutlery 发表于 2025-3-23 01:41:43
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