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Chromatin Proteins and Transcription Factors as Therapeutic Targets /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Donev, Rossen (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Cambridge, MA : Academic Press is an imprint of Elsevier, 2017.
Colección:Advances in protein chemistry and structural biology ; v. 107.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Chromatin Proteins and Transcription Factors as Therapeutic Targets /  |c edited by Rossen Donev. 
264 1 |a Cambridge, MA :  |b Academic Press is an imprint of Elsevier,  |c 2017. 
300 |a 1 online resource (xvi, 369 pages :  |b color illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Advances in protein chemistry and structural biology ;  |v volume 107 
546 |a Text in English. 
500 |a Includes indexes. 
588 0 |a Online resource; title from PDF title page (ScienceDirect, viewed February 24, 2017). 
505 8 |a 2.2.1. Posttranslational Acetylation2.2.2. Oxidation; 2.3. HMGB1-Receptor Families; 2.3.1. Receptor for Advanced Glycation End Products; 2.3.2. Toll-Like Receptors; 2.3.3. Recently Discovered HMGB1 Receptors; 3. HMGB1 in the Nucleus-An Architectural Factor; 3.1. Nucleolar Functions; 3.1.1. DNA Replication, Repair, and V(D)J Recombination; 3.1.2. Gene Transcription Transfer and Delivery; 3.1.3. Nucleosome Structure and Dynamics; 3.1.4. Telomere Homeostasis; 3.2. HMGB1 as a Damage Recognition Protein Mediating the Antitumor Effect of the Chemotherapeutic Drug cis-Platin 
505 8 |a 3.3. HMGB1 Protein-An Important Player in cis-platin-Based Therapy3.3.1. HMGB1 Affects the Repair of DNA Damaged by the Antitumor Drug cis-Platin In Vitro; 3.3.2. The Impact of HMGB1 Protein for the Repair Potential of Human Cancer Cell Lines: A Significant Issue for Therapeut ... ; 4. HMGB1 Outside the Cell; 4.1. HMGB1 as a Signaling Molecule; 4.2. HMGB1 and Diseases; 5. HMGB1 as a Therapeutic Target; 5.1. Antibody-Based Targeting; 5.2. Peptides and Protein Inhibitors of HMGB1; 5.3. Blockage of HMGB1-Receptor Signaling; 5.4. Small Molecules Inhibiting HMGB1 
504 |a Includes bibliographical references and indexes. 
650 0 |a Chromatin. 
650 0 |a Transcription factors. 
650 6 |a Chromatine.  |0 (CaQQLa)201-0062726 
650 6 |a Facteurs de transcription.  |0 (CaQQLa)201-0242208 
650 7 |a SCIENCE  |x Life Sciences  |x Biochemistry.  |2 bisacsh 
650 7 |a Chromatin  |2 fast  |0 (OCoLC)fst00859922 
650 7 |a Transcription factors  |2 fast  |0 (OCoLC)fst01154564 
700 1 |a Donev, Rossen,  |e editor. 
776 0 8 |i Print version:  |t Chromatin Proteins and Transcription Factors as Therapeutic Targets.  |d Cambridge, MA : Academic Press is an imprint of Elsevier, 2017  |z 0128123907  |z 9780128123904  |w (OCoLC)959869209 
830 0 |a Advances in protein chemistry and structural biology ;  |v v. 107. 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/bookseries/18761623/107  |z Texto completo 
880 8 |6 505-00/(S  |a 7. Effects of the Mesenchymal Cell-State Change on Innate Responses7.1. Dysregulation of Innate Signaling Pathways; 7.2. Epigenetic Silencing of Antiviral Interferons; 8. Therapeutic Targets in the RelA-Triggered Innate/Fibrotic Pathway; 8.1. NFκB/RelA; 8.2. Cyclin-Dependent Kinase 9; 8.3. Bromodomain-Containing Protein 4; 8.4. EZH2 of the PRC2 Repressor Complex; 9. Discussion and Outlook; Acknowledgments; References; Chapter Two: HMGB1 Protein: A Therapeutic Target Inside and Outside the Cell; 1. Introduction; 2. HMGB1-General Overview; 2.1. Structure; 2.2. Posttranslational Modifications 
880 8 |6 505-00/(S  |a 5.5. Oligonucleotide (ODN)-Based HMGB1 Inhibitors6. HMGB1 as a Target of miRs; 6.1. HMGB1 as a Direct Target of miRs; 6.2. HMGB1 as a Regulator of miR Expression; 7. Concluding Remarks; References; Chapter Three: Targeting IKK and NF-κB for Therapy; 1. IKK and NF-κB Signaling; 2. NF-κB Target Gene Specificity; 3. NF-κB in Inflammation, Survival, and Proliferation; 4. IKK and NF-κB Signaling in Disease; 5. Targeting IKK and NF-κB Signaling; 5.1. Receptor Inhibition; 5.2. Adaptor Inhibition as a Potential Strategy; 5.3. IKK Inhibition; 5.4. IκB Stabilization; 5.5. Blocking Nuclear Translocation 
880 0 |6 505-00/(S  |a Front Cover; Chromatin Proteins and Transcription Factors as Therapeutic Targets; Copyright; Contents; Contributors; Preface; Chapter One: Targeting Chromatin Remodeling in Inflammation and Fibrosis; 1. Inflammation Initiation in Mucosal Surfaces; 2. Central Role of NFκB in Regulating the Innate Immune Response; 3. Mechanisms of Inducible Gene Expression; 4. Transcriptional Elongation in Rapid Inflammatory Responses; 5. Mechanisms Linking Chronic Inflammation to Mesenchymal Transition and Airway Fibrosis; 6. The RelA-BRD4 Pathway Links Inflammation, Fibrosis, and Airway Remodeling