Cystic Fibrosis Methods and Protocols

Name: Cystic Fibrosis Methods and Protocols
Brand: Humana Press Inc.
SKU: 9780896038974
Price: 889.56 RON
Availability: InStock

Autor: William R. Skach

Limbă:

Legare: Copertă tare

Editura: Humana Press Inc.

Disponibilitate: În depozitul extern în cantități mici

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889.56 lei

Since the cloning of the cystic fibrosis transmembrane conductance re- lator (CFTR) nearly a decade...

Informații despre carte

Autor

William R. Skach

Limbă

engleză

Legare

Carte - Copertă tare

Publicat

2002

Pagini

615

EAN

9780896038974

ISBN

0896038971

Enbook ID

01400893

Editura

Humana Press Inc.

Greutate

1084

Dimensiuni

155 x 235 x 36

Descriere completă

Since the cloning of the cystic fibrosis transmembrane conductance re- lator (CFTR) nearly a decade ago, cystic fibrosis (CF) research has witnessed a dramatic expansion into new scientific areas. Basic researchers, clinicians, and patients increasingly rely on fundamental techniques of genetics, molecular biology, electrophysiology, biochemistry, cell biology, microbiology, and immunology to understand the molecular basis of this complex disease. Research into the pathophysiology of CF has established numerous paradigms of ion channel dysfunction that extend from inflammation and infection in the airways of patients to basic mechanisms of protein processing and regulation in intracellular components. With these rapid advances has come an increasing need for research scientists to understand and utilize a growing array of basic laboratory tools. This volume of Methods in Molecular Medicine, Cystic Fibrosis Methods and Protocols satisfies that need by providing detailed protocols for the laboratory techniques used throughout CF research. From electrophysiology and cell biology, to animal models and gene therapy, the comprehensive set of methods covered here provide step-by-step instructions needed for investigators to incorporate new approaches into their research programs. Contributions have been chosen to reflect the rich diversity of techniques and to provide a cohesive framework for understanding challenges that are currently at the forefront of CF research. It is hoped that this volume will serve as a valuable reference that will not only foster interdisciplinary investigations into current problems encountered in CF, but also facilitate the translation of new scientific discoveries into clinical solutions.

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