Chromatin Readers in Health and Disease, Volume 32, a new release in the Translational Epigenetics series, gathers and makes actionable our current understanding of how chromatin readers regulate access to genetic information, and how their aberrant regulation can contribute to human pathologies. Chromatin readers discussed include 14-3-3 Dinshaw, ADD, Ankyrin, BAH, BET, BIR, BRCT, bromodomains and Kac readers, chromodomains and chromobarrel readers, citrullination readers, macrodomains and poly-ADP-ribose readers, MBT, PHD and double PHD, PWWP, SUMO (H4K12) readers, Tudor and TTD, UDR and ubiquitin, WD40, YEATS (crotonyl reader)?, MBD, SRA, and Methyl-RNA readers.
In the book, more than a dozen leaders in the field examine a range of protein readers, their relationship to human disease, and the early therapeutics that act as chromatin signaling factors to treat cancers and Huntington's disease, among other disorders.
- Enables researchers and clinicians to understand chromatin signaling mechanisms that regulate gene expression through chromatin readers
- Highlights the role of chromatin readers in a variety of human pathologies, as well as early therapeutics that act on chromatin signaling
- Includes chapter contributions from international leaders in the field
1. ADD domains a regulatory hub in chromatin biology and disease
2. BAH
3. BIR
4. BRCT Domains as Chromatin Readers: Structure, Function, and Clinical
Implications
5. The bromodomain acyl-lysine readers in human health and disease
6. Chromodomains
7. CW-type zinc fingers
8. Macrodomains and PAR readers
9. MBT
10. PHD and double PHD finger
11. PWWP
12. SPIN repeats and human pathologies
13. Tudor and TTD
14. UDR and Ubiquitin
15. WD40
16. YEATS
17. Multivalent readers and interplay among different readers
18. DNA Methylation and Reader- or Writer-Proteins: Differentiation and
Disease
19. R-loops readers
20. CUT&RUN and CUT&Tag: Low-input methods for genome-wide mapping of
chromatin proteins
Dr. Olivier Binda is a Researcher at the University of Ottawa, specializing in epigenetics and gene expression as it relates to human diseases. Dr. Binda co-edited Chromatin Signaling and Diseases (Elsevier 2016), a volume in Elseviers Translational Epigenetics series, and has published 20 scientific papers in such peer reviewed journals as the Molecular Cell, Journal of Biological Chemistry, Biochemistry, Epigenetics, Oncogene, Scientific Reports, and Stem Cell Research. In past positions he has served as a postdoctoral fellow at McGill University and Stanford University, and he completed his PhD in Biochemistry at McGill University in 2007.
Affiliations and expertise
University of Ottawa, Department of Cellular and Molecular Medicine, Ottawa, CANADA.
Dr. Tollefsbol is a Distinguished Professor at the University of Alabama at Birmingham. He holds doctorates in molecular biology and osteopathic medicine, trained with National Academy of Science members and has over 200 peer-reviewed publications. Reports highlighting the translatability to the lay public of the discoveries made in his laboratory have appeared in international media representing >50 million readers. Dr. Tollefsbol has been featured as an Investigator in the Spotlight by the NIH as well as a Scientist in the Spotlight by ScienceNow. He is an Associate Editor for Frontiers in Genetics, a contributor to Lewins GENES classic textbook and Lead Editor for Elseviers Translational Epigenetics Series. Dr. Tollefsbol has been named a Highly Ranked Scholar” worldwide (ScholarGPS). He has been invited for numerous endowed keynote presentations, his research has been highlighted in eScience News and ScienceDaily and he has published 20 scholarly books on topics related to his research.
Lisainfo e-raamatute kohta