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SCIDIR_ocn973396828 |
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OCoLC |
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20231120112214.0 |
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170222s2017 maua ob 001 0 eng d |
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|a 0128123915
|q (electronic bk.)
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|a Chromatin Proteins and Transcription Factors as Therapeutic Targets /
|c edited by Rossen Donev.
|
264 |
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1 |
|a Cambridge, MA :
|b Academic Press is an imprint of Elsevier,
|c 2017.
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300 |
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|a 1 online resource (xvi, 369 pages :
|b color illustrations
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336 |
|
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|a text
|b txt
|2 rdacontent
|
337 |
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|a computer
|b c
|2 rdamedia
|
338 |
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|a online resource
|b cr
|2 rdacarrier
|
490 |
1 |
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|a Advances in protein chemistry and structural biology ;
|v volume 107
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546 |
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|a Text in English.
|
500 |
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|a Includes indexes.
|
588 |
0 |
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|a Online resource; title from PDF title page (ScienceDirect, viewed February 24, 2017).
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505 |
8 |
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|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
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505 |
8 |
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|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
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504 |
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|a Includes bibliographical references and indexes.
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650 |
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0 |
|a Chromatin.
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650 |
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0 |
|a Transcription factors.
|
650 |
|
6 |
|a Chromatine.
|0 (CaQQLa)201-0062726
|
650 |
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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 |
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|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 |
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|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
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880 |
0 |
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|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
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