Bradshaw / Dennis | Regulation of Organelle and Cell Compartment Signaling | Buch | 978-0-12-382213-0 | sack.de

Buch, Englisch, 550 Seiten, Format (B × H): 218 mm x 274 mm, Gewicht: 1592 g

Bradshaw / Dennis

Regulation of Organelle and Cell Compartment Signaling


Erscheinungsjahr 2011
ISBN: 978-0-12-382213-0
Verlag: Elsevier Science

Buch, Englisch, 550 Seiten, Format (B × H): 218 mm x 274 mm, Gewicht: 1592 g

ISBN: 978-0-12-382213-0
Verlag: Elsevier Science


This must-have cell signaling title will appeal to researchers across molecular biology, biochemistry, cell biology and genetics. The articles are written and edited by experts in the field and emphasize signaling to and from intracellular compartments including transcriptional responses to cytoplasmic and nuclear signaling events, chromatin remodeling and stress responses, the regulation of endoplasmic reticulum function, control of cell cycle progression and apoptosis and the modulation of the activities of mitochondria and other organelles.

Bradshaw / Dennis Regulation of Organelle and Cell Compartment Signaling jetzt bestellen!

Zielgruppe


<p>Professionals, researchers and graduate students in molecular biology, biochemistry, cell biology, biomedicine, structural biology, systems biology, and genetics.</p>

Weitere Infos & Material


244 Nuclear Receptor Coactivators

245 Corepressors in Mediating Repression by Nuclear Receptors

246 Steroid Hormone Receptor Signaling

247 Role of COUP-TFII in Congenital Diaphragmatic Hernia

248 Nuclear Receptors in Drosophila melanogaster

249 JAK-STAT Signaling

250 FOXO Transcription Factors: Key Targets of the PI3K-Akt Pathway

251 The Multi-gene Family of Transcription Factor AP-1

252 NF-KB: a Key Integrator of Cell Signaling

253 Transcriptional Regulation via the cAMP Responsive Activator CREB

254 The NFAT Family: Structure, Regulation and Biological Functions

255 Ubiquitination/Proteasome

256 The SMADs

257 Complexity of Stress Signaling

258 Signal Transduction in the Escherichia coli SOS Response

259 Oxidative Stress and Free Radical Signal Transduction

260 Screening Approaches to Identify Genes Required for DNA Double-Strand Break

261 Radiation Responses in Drosophila

262 Double-strand Break Recognition and its Repair by Non-homologous End Joining

263 ATM-Mediated Signaling Defends the Integrity of the Genome

264 Signaling to the p53 Tumor Suppressor through Pathways

265 The p53 Master Regulator and Rules of Engagement with Target Sequences

266 Nuclear and Cytoplasmic Functions of Abl Tyrosine Kinase

267 Radiation-induced Cytoplasmic Signaling

268 The Heat-Shock Response and the Stress of Misfolded Proteins

269 Hypoxia-Mediated Signaling Pathways

270 Regulation of mRNA Turnover by Cellular Stress

271 Oncogenic Stress Responses

272 Ubiquitin and FANC Stress Responses

273 Stress and g -H2AX

274 Translational Control by Amino Acids and Energy

275 Translation Control and Insulin Signaling

276 ER and oxidative stress: Implications in disease

277 Regulation of mRNA Turnover

278 Signaling to Cytoplasmic Polyadenylation and Translation

279 Translational Control in Invertebrate Development

280 The Role of Alternative Splicing During the Cell Cycle and Programmed Cell Death

281 Signaling Pathways that Mediate Translational Control of Ribosome Recruitment

282 The SWI/SNF and RSC Nucleosome Remodeling Complexes

283 ISWI Chromatin Remodeling Complexes

284 The INO80 Chromatin Remodeling Complex

285 Histone Acetylation Complexes

286 Regulation of Histone Deacetylase Activities and Functions by Phosphorylation and

287 Histone Methylation: Chemically Inert But Chromatin Dynamic

288 Histone Phosphorylation: Chromatin Modifications

289 Histone Variants: Signaling or Structural Modules?

290 Silent Chromatin Formation and Regulation in the Yeast Saccharomyces cerevisiae

291 Gene Silencing and Chromatin Modification by Polycomb Complexes

292 Histone Ubiquitination

293 Chromatin-mediated Control of Gene Expression in Innate Immunity and Inflammation


Dennis, Edward A
Edward A. Dennis is Distinguished Professor and former Chair of the Department of Chemistry and Biochemistry and Professor in the Department of Pharmacology in the School of Medicine at the University of California, San Diego. He is also Editor-in-Chief of the Journal of Lipid Research.

Bradshaw, Ralph A
Ralph A. Bradshaw is Professor Emeritus in the Department of Physiology and Biophysics at the University of California, Irvine. Prior to that he was on the faculty of the Department of Biological Chemistry, Washington University, and Professor and Chair of the Department of Biological Chemistry, University of California Irvine. He presently is Professor of Pharmacology at the University of California, San Diego. He served as president of FASEB, was the founding president of the Protein Society and was the treasurer of the ASBMB. He was the founding editor of Molecular and Cellular Proteomics. His research has focused on protein chemistry and proteomics, with emphasis on the structure and function of growth factors and their receptors, particularly nerve growth factor and ?broblast growth factor, and the involvement of receptor tyrosine kinases in cell signaling. He has also studied the role of proteolytic processing and N-terminal modi?cation in protein stability and turnover.

Edited by Ralph A. Bradshaw, Department of Chemistry and Pharmaceutical Chemistry; and Mass Spectrometry Facility, University of California, San Francisco, Department of Physiology and Biophysics, College of Medicine, University of California, Irvine, Irvine, CA. and Edward A. Dennis, Department of Chemistry and Biochemistry and Department of Pharmacology in the School of Medicine at the University of California, San Diego



Ihre Fragen, Wünsche oder Anmerkungen
Vorname*
Nachname*
Ihre E-Mail-Adresse*
Kundennr.
Ihre Nachricht*
Lediglich mit * gekennzeichnete Felder sind Pflichtfelder.
Wenn Sie die im Kontaktformular eingegebenen Daten durch Klick auf den nachfolgenden Button übersenden, erklären Sie sich damit einverstanden, dass wir Ihr Angaben für die Beantwortung Ihrer Anfrage verwenden. Selbstverständlich werden Ihre Daten vertraulich behandelt und nicht an Dritte weitergegeben. Sie können der Verwendung Ihrer Daten jederzeit widersprechen. Das Datenhandling bei Sack Fachmedien erklären wir Ihnen in unserer Datenschutzerklärung.