- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1756-8935
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Generation of bivalent chromatin domains during cell fate decisions ; volume:4 ; number:1 ; day:6 ; month:6 ; year:2011 ; pages:1-12 ; date:12.2011
Epigenetics & chromatin ; 4, Heft 1 (6.6.2011), 1-12, 12.2011
- Creator
-
De Gobbi, Marco
Garrick, David
Lynch, Magnus
Vernimmen, Douglas
Hughes, Jim R.
Goardon, Nicolas
Luc, Sidinh
Lower, Karen M.
Sloane-Stanley, Jacqueline A.
Pina, Cristina
Soneji, Shamit
Renella, Raffaele
Enver, Tariq
Taylor, Stephen
Jacobsen, Sten Eirik W.
Vyas, Paresh
Gibbons, Richard J.
Higgs, Douglas R.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/1756-8935-4-9
- URN
-
urn:nbn:de:101:1-2021081621193411693317
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:52 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- De Gobbi, Marco
- Garrick, David
- Lynch, Magnus
- Vernimmen, Douglas
- Hughes, Jim R.
- Goardon, Nicolas
- Luc, Sidinh
- Lower, Karen M.
- Sloane-Stanley, Jacqueline A.
- Pina, Cristina
- Soneji, Shamit
- Renella, Raffaele
- Enver, Tariq
- Taylor, Stephen
- Jacobsen, Sten Eirik W.
- Vyas, Paresh
- Gibbons, Richard J.
- Higgs, Douglas R.
- SpringerLink (Online service)
Other Objects (12)
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Mechanisms of force-mediated regulation of transcription, chromatin remodeling and cell fate decisions
A low-input high resolution sequential chromatin immunoprecipitation method captures genome-wide dynamics of bivalent chromatin
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Stochastic T-cell fate decisions
Binding the boundaries of chromatin domains
Chromatin accessibility dynamics during cell fate reprogramming
Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer
Dynamic simulation of active, inactive chromatin domains
Identification of alternative topological domains in chromatin
Poised chromatin and bivalent domains facilitate the mitosis-to-meiosis transition in the male germline
Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state
Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state
Mechanisms of force-mediated regulation of transcription, chromatin remodeling and cell fate decisions
A low-input high resolution sequential chromatin immunoprecipitation method captures genome-wide dynamics of bivalent chromatin
„Stochastic T cell fate decisions“
Stochastic T-cell fate decisions
Binding the boundaries of chromatin domains
Chromatin accessibility dynamics during cell fate reprogramming
Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer
Dynamic simulation of active, inactive chromatin domains
Identification of alternative topological domains in chromatin
Poised chromatin and bivalent domains facilitate the mitosis-to-meiosis transition in the male germline
Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state
Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state
Mechanisms of force-mediated regulation of transcription, chromatin remodeling and cell fate decisions
A low-input high resolution sequential chromatin immunoprecipitation method captures genome-wide dynamics of bivalent chromatin
„Stochastic T cell fate decisions“
Stochastic T-cell fate decisions
Binding the boundaries of chromatin domains
Chromatin accessibility dynamics during cell fate reprogramming
Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer
Dynamic simulation of active, inactive chromatin domains