Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1756-8935
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state ; volume:10 ; number:1 ; day:25 ; month:9 ; year:2017 ; pages:1-19 ; date:12.2017
Epigenetics & chromatin ; 10, Heft 1 (25.9.2017), 1-19, 12.2017
- Classification
-
Biowissenschaften, Biologie
- Creator
- Contributor
- DOI
-
10.1186/s13072-017-0153-1
- URN
-
urn:nbn:de:1111-2017112339432
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:31 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
- Mauser, Rebekka
- Kungulovski, Goran
- Keup, Corinna
- Reinhardt, Richard
- Jeltsch, Albert
- SpringerLink (Online service)
Other Objects (12)
Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state
Generation of bivalent chromatin domains during cell fate decisions
Biochemical investigations of multivalent chromatin reading domains
Poised chromatin and bivalent domains facilitate the mitosis-to-meiosis transition in the male germline
A low-input high resolution sequential chromatin immunoprecipitation method captures genome-wide dynamics of bivalent chromatin
Binding the boundaries of chromatin domains
Development of artificial single and double reading domains to analyze chromatin modification patterns
Dynamic simulation of active, inactive chromatin domains
Identification of alternative topological domains in chromatin
Chromatin
Analysis of three-dimensional chromatin packing domains by chromatin scanning transmission electron microscopy (ChromSTEM)
Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer
Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state
Generation of bivalent chromatin domains during cell fate decisions
Biochemical investigations of multivalent chromatin reading domains
Poised chromatin and bivalent domains facilitate the mitosis-to-meiosis transition in the male germline
A low-input high resolution sequential chromatin immunoprecipitation method captures genome-wide dynamics of bivalent chromatin
Binding the boundaries of chromatin domains
Development of artificial single and double reading domains to analyze chromatin modification patterns
Dynamic simulation of active, inactive chromatin domains
Identification of alternative topological domains in chromatin
Chromatin
Analysis of three-dimensional chromatin packing domains by chromatin scanning transmission electron microscopy (ChromSTEM)
Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer
Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state
Generation of bivalent chromatin domains during cell fate decisions
Biochemical investigations of multivalent chromatin reading domains
Poised chromatin and bivalent domains facilitate the mitosis-to-meiosis transition in the male germline
A low-input high resolution sequential chromatin immunoprecipitation method captures genome-wide dynamics of bivalent chromatin
Binding the boundaries of chromatin domains
Development of artificial single and double reading domains to analyze chromatin modification patterns
Dynamic simulation of active, inactive chromatin domains
Identification of alternative topological domains in chromatin
Chromatin
Analysis of three-dimensional chromatin packing domains by chromatin scanning transmission electron microscopy (ChromSTEM)