Cystic Fibrosis : Diagnosis and Protocols, Volume II: Methods and Resources to Understand Cystic Fibrosis /
Autor Corporativo: | |
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Otros Autores: | , |
Formato: | eBook |
Lenguaje: | English |
Publicado: |
Totowa, NJ :
Humana Press : Imprint: Humana,
2011.
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Edición: | 1st ed. 2011. |
Colección: | Methods in Molecular Biology,
742 |
Materias: |
Tabla de Contenidos:
- Introduction to Part I: Overview of Approaches to Study Cystic Fibrosis Pathophysiology
- Imaging CFTR Protein Localization in Cultured Cells and Tissues
- CFTR Regulation of Epithelial Sodium Channel
- Methods for Evaluating Inflammation in Cystic Fibrosis
- Methods for ASL Measurements and Mucus Transport Rates in Cell Cultures
- Measurement of Fluid Secretion from Intact Airway Submucosal Glands
- Measurements of Intracellular Calcium Signals in Polarized Primary Cultures of Normal and Cystic Fibrosis Human Airway Epithelia
- Identification and Quantification of Mucin Expression
- Methods to Classify Bacterial Pathogens in Cystic Fibrosis
- Approaches to Study Differentiation and Repair of Human Airway Epithelial Cells
- Introduction to Part II: Omics in the Biology of Cystic Fibrosis
- Microarray mRNA Expression Profiling to Study Cystic Fibrosis
- Quantitative Differential Proteomics of Cystic Fibrosis Cell Models by SILAC (Stable Isotope Labelling in Cell Culture)
- Application of Mass Spectrometry to Study Proteomics and Interactomics in Cystic Fibrosis
- Functional Genomics Assays to Study CFTR Traffic and ENaC Function
- New Lipidomic Approaches in Cystic Fibrosis
- Introduction to Part III: Resources for CFTR Research
- Primary Epithelial Cell Models for Cystic Fibrosis Research
- Comparative Biology of Cystic Fibrosis Animal Models
- CFTR Folding Consortium: Methods Available for Studies of CFTR Folding and Correction
- Evaluation of the Disease Liability of CFTR Variants.