Chromatin Signaling and Diseases

Forfatter: info mangler
Bog
  • Format
  • Bog, hardback
  • Engelsk

Beskrivelse

Chromatin Signaling and Diseases covers the molecular mechanisms that regulate gene expression, which govern everything from embryonic development, growth, and human pathologies associated with aging, such as cancer. This book helps researchers learn about or keep up with the quickly expanding field of chromatin signaling. After reading this book, clinicians will be more capable of explaining the mechanisms of gene expression regulation to their patients to reassure them about new drug developments that target chromatin signaling mechanisms. For example, several epigenetic drugs that act on chromatin signaling factors are in clinical trials or even approved for usage in cancer treatments, Alzheimer's, and Huntington's diseases. Other epigenetic drugs are in development to regulate various class of chromatin signaling factors. To keep up with this changing landscape, clinicians and doctors will need to stay familiar with genetic advances that translate to clinical practice, such as chromatin signaling. Although sequencing of the human genome was completed over a decade ago and its structure investigated for nearly half a century, molecular mechanisms that regulate gene expression remain largely misunderstood. An emerging concept called chromatin signaling proposes that small protein domains recognize chemical modifications on the genome scaffolding histone proteins, facilitating the nucleation of enzymatic complexes at specific loci that then open up or shut down the access to genetic information, thereby regulating gene expression. The addition and removal of chemical modifications on histones, as well as the proteins that specifically recognize these, is reviewed in Chromatin Signaling and Diseases. Finally, the impact of gene expression defects associated with malfunctioning chromatin signaling is also explored.

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Detaljer
  • SprogEngelsk
  • Sidetal480
  • Udgivelsesdato06-09-2016
  • ISBN139780128023891
  • Forlag Academic Press Inc
  • FormatHardback
Størrelse og vægt
  • Vægt1540 g
  • coffee cup img
    10 cm
    book img
    21,6 cm
    27,6 cm

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    Stress DNA Cancer Aging Gene expression. Pharmacology Transcription DNA repair Yeast Gene silencing Infection Cell division DNA damage Hats Phosphorylation Therapeutics Chromatin Inhibitors Crosstalk Parasites Bile acids Endoplasmic reticulum Histones Mitosis Non-coding RNA DNA Methylation Reader Saga Epigenetics Indole MicroRNA HP1 Transcription factor Nuclear receptors Epigenome Ubiquitination Senescence Short Chain Fatty Acids Oncogene Programmed cell death Kinase Chromatin dynamics Operon Chromatin modifications Human disease Gene transcription Epigenetic Therapeutic Histone modifications PTMs Outline Chromatin structure Histone modification Keyword EMT DNA transcription Signaling pathway Unfolded Protein response Phosphatase Biomarker M¿ll Prognostic BRD4 Amino acid Proteostasis Histone methylation Pancreatic cancer Histone Tumor suppressor Virulence DNA damage response Lysine Polycomb Nucleosome EZH2 H3K9 methylation HDACs Acetylation Multivalent Alcoholic liver disease (ALD)Epigenetic reprogramming Arginine methylation Aromatic cage Cancer stem-like cells Cancer cell plasticity Bmi1 Chromatin structure and dynamics Chromatin function Chromo domain Bacterial metabolite Arginine residues Chromo shadow domain BET bromodomain Bromodomain Diagnostic DNA methylation Double-strand break repair Chromatin remodeling enzymes Chromo helicase Epigenetic diseases H3K4 methylation H4K20 methylation H3K36 methylation Histone marks Gcn5 (general control nonderepressible 5)Histone acetyltransferases (HATs)Lysine acetyltransferase Histone lysine methyltransferases (HKMTs)Lysine methylation Histone mark writers H3K27 methylation Histone-modifying enzymes Histone tails H3K79 methylation IDH Epigenetic drugs Lysine demethylases Methyl-arginine Methyl-lysine Nucleosome assembly Metabolome Phd Finger PHD and YEATS domains Posttranslational modification (PTM)Protein arginine methyltransferases (PRMTs)Precision medicine Receiver operating characteristic Royal Family Human Embryonic Stem Cell SWI/SNF Synergic inhibition Methyllysine reader SUZ12 Lysine methylation Mechanisms of adaptation Trithorax SWI/SNF complex Tudor domain

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