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Checkpoint Responses in Cancer Therapy: Cancer Drug Discovery and Development

Editat de Wei Dai
en Limba Engleză Paperback – 19 noi 2010
Extensive research has uncovered a set of molecular surveillance mechanisms – commonly called “checkpoints” – which tightly monitor cell-cycle processes. Today’s anticancer drug development has identified many of these cell-cycle checkpoint molecules as effective targets. Research now promises to uncover a new generation of anticancer drugs with improved therapeutic indices based on their ability to target emerging checkpoint components. Checkpoint Responses in Cancer Therapy summarizes the advances made over the past 20 years, identifying components of cell-cycle checkpoints and their molecular regulation during checkpoint activation and validating the use of checkpoint proteins as targets for the development of anticancer drugs. This book’s distinguished panel of authors takes a close look at topics ranging from the major molecular players affecting DNA synthesis and the response to DNA damage to advances made in the identification of chemical compounds capable of inhibiting individual mitotic kinases. Illuminating and authoritative, Checkpoint Responses in Cancer Therapy offers a critical summary of findings for researchers in the pharmaceutical and biotechnology industries and a valuable resource for academic scientists in cancer research and the study of cell-cycle regulation, signal transduction and apoptosis.
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Specificații

ISBN-13: 9781617378478
ISBN-10: 161737847X
Pagini: 314
Ilustrații: XIV, 314 p. 33 illus., 3 illus. in color.
Dimensiuni: 155 x 235 x 18 mm
Greutate: 0.46 kg
Ediția:Softcover reprint of hardcover 1st ed. 2008
Editura: Humana Press Inc.
Colecția Humana
Seria Cancer Drug Discovery and Development

Locul publicării:Totowa, NJ, United States

Public țintă

Research

Cuprins

RB-Pathway.- Targeting the p53/MDM2 Pathway for Cancer Therapy.- DNA Topoisomerases as Targets for the Chemotherapeutic Treatment of Cancer.- Targeting ATM/ATR in the DNA Damage Checkpoint.- Compounds that Abrogate the G2 Checkpoint.- CDK Inhibitors as Anticancer Agents.- CHFR as a Potential Anticancer Target.- Antimicrotubule Agents.- Kinesin Motor Inhibitors as Effective Anticancer Drugs.- Targeting the Spindle Checkpoint in Cancer Chemotherapy.- Antiproliferation Inhibitors Targeting Aurora Kinases.- Plks as Novel Targets for Cancer Drug Design.- Do Histone Deacetylase Inhibitors Target Cell Cycle Checkpoints that Monitor Heterochromatin Structure?.

Textul de pe ultima copertă

Extensive research has uncovered a set of molecular surveillance mechanisms – commonly called "checkpoints" – which tightly monitor cell-cycle processes. Today’s anticancer drug development has identified many of these cell-cycle checkpoint molecules as effective targets. Research now promises to uncover a new generation of anticancer drugs with improved therapeutic indices based on their ability to target emerging checkpoint components. Checkpoint Responses in Cancer Therapy summarizes the advances made over the past 20 years, identifying components of cell-cycle checkpoints and their molecular regulation during checkpoint activation and validating the use of checkpoint proteins as targets for the development of anticancer drugs. This book’s distinguished panel of authors takes a close look at topics ranging from the major molecular players affecting DNA synthesis and the response to DNA damage to advances made in the identification of chemical compounds capable of inhibiting individual mitotic kinases. Illuminating and authoritative, Checkpoint Responses in Cancer Therapy offers a critical summary of findings for researchers in the pharmaceutical and biotechnology industries and a valuable resource for academic scientists in cancer research and the study of cell-cycle regulation, signal transduction and apoptosis.

Caracteristici

First book to summarize recent advances in identifying components of cell-cycle checkpoints and validating the use of checkpoint proteins as targets for the development of anticancer drugs Distinguished authors write on topics that range from the molecular players affecting DNA synthesis and the response to DNA damage, to advances in the identification of inhibitors for individual mitotic kinases Offers a summary of their findings for researchers in the pharmaceutical and biotechnology industries Valuable resource for cancer researchers studying of cell-cycle regulation, signal transduction, and apoptosis