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Mammalian TRP Channels as Molecular Targets
Novartis Foundation
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Description for Mammalian TRP Channels as Molecular Targets
Transient Receptor Potential (TRP) genes were originally identified as encoding critical components of phototransduction in Drosophila. Since the discovery of the first mammalian transient receptor potential channel (TRPC) some eight years ago, more than 20 mammalian homologues have been reported. Series: Novartis Foundation Symposia. Num Pages: 286 pages, Illustrations. BIC Classification: PSAK; PSVW7. Category: (P) Professional & Vocational. Dimension: 237 x 164 x 19. Weight in Grams: 588.
This book brings together contributions from key investigators in the area of Transient Receptor Potential (TRP) channel structure and function. It covers the structure, function and regulation of mammalian TRP channels and mechanisms of signal transduction. The discussions indicate research that would improve understanding of the role of TRP channels in normal cellular physiology, the involvement of TRP channels in disease states and their potential use as molecular targets for novel therapeutic agents.
This book brings together contributions from key investigators in the area of Transient Receptor Potential (TRP) channel structure and function. It covers the structure, function and regulation of mammalian TRP channels and mechanisms of signal transduction. The discussions indicate research that would improve understanding of the role of TRP channels in normal cellular physiology, the involvement of TRP channels in disease states and their potential use as molecular targets for novel therapeutic agents.
Product Details
Publication date
2004
Publisher
John Wiley and Sons Ltd United Kingdom
Number of pages
286
Condition
New
Series
Novartis Foundation Symposia
Number of Pages
288
Format
Hardback
Place of Publication
New York, United States
ISBN
9780470862544
SKU
V9780470862544
Shipping Time
Usually ships in 15 to 20 working days
Ref
99-15
About Novartis Foundation
Derek J. Chadwick and Jamie A. Goode are editors for Mammalian TRP Channels as Molecular Targets and other scientific titles.
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