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Cyclin-Depende
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- Compralo SubitoCyclin-Dependent Kinase (CDK) Inhibitors by P.K. Vogt & S.I. Reed HC
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Ritiro:
Ritiro gratuito dell'oggetto in zona da Woburn, Massachusetts, Stati Uniti.
Spedizione:
US $4,40 (circa EUR 3,78) USPS Media MailTM.
Oggetto che si trova a: Woburn, Massachusetts, Stati Uniti
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Consegna prevista tra il mar 22 lug e il lun 28 lug
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Restituzioni entro 30 giorni. Le spese di spedizione del reso sono a carico dell'acquirente..
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Numero oggetto eBay:395250474583
Specifiche dell'oggetto
- Condizione
- ISBN
- 9783540634294
Informazioni su questo prodotto
Product Identifiers
Publisher
Springer
ISBN-10
3540634290
ISBN-13
9783540634294
eBay Product ID (ePID)
415331
Product Key Features
Number of Pages
Xii, 169 Pages
Language
English
Publication Name
Cyclin-Dependent Kinase (Cdk) Inhibitors
Publication Year
1997
Subject
Life Sciences / Molecular Biology, Immunology, Life Sciences / Biochemistry, Oncology
Type
Textbook
Subject Area
Science, Medical
Series
Current Topics in Microbiology and Immunology Ser.
Format
Hardcover
Dimensions
Item Weight
14.8 Oz
Item Length
9.3 in
Item Width
6.1 in
Additional Product Features
Intended Audience
Scholarly & Professional
Series Volume Number
227
Number of Volumes
1 vol.
Illustrated
Yes
Synopsis
More than 10 years ago, the discovery of cyclin-dependent ki nases (Cdks) ushered in a new era in the understanding of cell proliferation and its control. Not only were both of the known cell cycle transitions, from G 1 to S phase and G2 to M phase, found to be dependent on these protein kinases, but the reg ulatory assumption intrinsic to cyclin-dependent kinases, a stable inactive catalytic subunit (the Cdk) and an unstable requisite positive regulatory activating subunit (the cyclin), led to a simple model for cell cycle control. Modulation of cyclin accumulation, and thereby Cdk activation, was proposed to be the overarching principle governing the passage through cell cycle phases. An other reality to emerge from the discovery of Cdks was the ex ceptional degree of evolutionary conservation maintained in the machinery and organization of proliferation control. Not only were Cdks shown to be structurally conserved between yeast and man, but mammalian Cdks could substitute functionally for the endogenous enzymes in a yeast cell. The problem of cell cycle control was thought to have been virtually solved. The ensuing years have provided a much more complex view of cell cycle control and the role and regulation of Cdks. The uncritical enthusiasm with which many of the ideas were em braced has required tempering. For example, although Cdks appear to be highly conserved phylogenetically, cyclins are much less so., More than 10 years ago, the discovery of cyclin-dependent ki nases (Cdks) ushered in a new era in the understanding of cell proliferation and its control. Not only were both of the known cell cycle transitions, from G 1 to S phase and G2 to M phase, found to be dependent on these protein kinases, but the reg ulatory assumption intrinsic to cyclin-dependent kinases, a stable inactive catalytic subunit (the Cdk) and an unstable requisite positive regulatory activating subunit (the cyclin), led to a simple model for cell cycle control. Modulation of cyclin accumulation, and thereby Cdk activation, was proposed to be the overarching principle governing the passage through cell cycle phases. An other reality to emerge from the discovery of Cdks was the ex ceptional degree of evolutionary conservation maintained in the machinery and organization of proliferation control. Not only were Cdks shown to be structurally conserved between yeast and man, but mammalian Cdks could substitute functionally for the endogenous enzymes in a yeast cell. The problem of cell cycle control was thought to have been virtually solved. The ensuing years have provided a much more complex view of cell cycle control and the role and regulation of Cdks. The uncritical enthusiasm with which many of the ideas were em braced has required tempering. For example, although Cdks appear to be highly conserved phylogenetically, cyclins are much less so."
LC Classification Number
QR180-189.5QH573-67
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