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Cystic Fibrosis Transmembrane Conductance Regulator
. Ed(S): Kirk, Kevin L. (Department Of Physiology And Biophysics, University Of Alabama At Birmingham, Usa); Dawson, David C. (Department Of Physiolo
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Description for Cystic Fibrosis Transmembrane Conductance Regulator
Hardback. The CFTR chloride channel is one of the important transport proteins in biology. This book addresses a select series of topics that relate to the function of CFTR, and the links between CFTR dysfunction and human disease - cystic fibrosis. It is designed for a readership with interests in CFTR, cystic fibrosis, ion channels, and ABC transporters. Editor(s): Kirk, Kevin L. (Department of Physiology and Biophysics, University of Alabama at Birmingham, USA); Dawson, David C. (Department of Physiology and Pharmacology, Oregon Health and Science University, Portland, USA). Series: Molecular Biology Intelligence Unit. Num Pages: 227 pages, biography. BIC Classification: PSB; PSF. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 19. Weight in Grams: 1110.
The CFTR chloride channel is one of the most well studied transport proteins in biology. Yet there remain many mysteries about the functional properties and biological roles of this ABC transporter. The Cystic Fibrosis Transmembrane Conductance Regulator addresses a select series of `hot' topics that relate to the function of CFTR, and the links between CFTR dysfunction and human disease (i.e., cystic fibrosis). The timeliness of these topics distinguishes this collection from previous volumes of this type. Given the general interest in CFTR, this collection will appeal to a broad readership with interests in CFTR, cystic fibrosis, ion channels and ... Read more
The CFTR chloride channel is one of the most well studied transport proteins in biology. Yet there remain many mysteries about the functional properties and biological roles of this ABC transporter. The Cystic Fibrosis Transmembrane Conductance Regulator addresses a select series of `hot' topics that relate to the function of CFTR, and the links between CFTR dysfunction and human disease (i.e., cystic fibrosis). The timeliness of these topics distinguishes this collection from previous volumes of this type. Given the general interest in CFTR, this collection will appeal to a broad readership with interests in CFTR, cystic fibrosis, ion channels and ... Read more
Product Details
Format
Hardback
Publication date
2003
Publisher
Springer Science+Business Media United States
Number of pages
227
Condition
New
Series
Molecular Biology Intelligence Unit
Number of Pages
215
Place of Publication
, United States
ISBN
9780306478376
SKU
V9780306478376
Shipping Time
Usually ships in 15 to 20 working days
Ref
99-15
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