Cystic Fibrosis : Diagnosis and Protocols, Volume II: Methods and Resources to Understand Cystic Fibrosis /

Detalles Bibliográficos
Autor Corporativo: SpringerLink (Online service)
Otros Autores: Amaral, Margarida D. (Editor ), Kunzelmann, Karl. (Editor )
Formato: eBook
Lenguaje:English
Publicado: Totowa, NJ : Humana Press : Imprint: Humana, 2011.
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.