A fellowship of Ring1 maintains AML stem cells

Polycomb repressive complex 1 (PRC1) and PRC2 are transcriptional repressors that function as key regulators of the self-renewal and differentiation (cell lineage specification) pathways in stem cells. In this issue of Blood, Shima et al1 report that 2 ubiquitin ligases (Ring1A and Ring1B), which ar...

Full description

Bibliographic Details
Main Author: Heery, David M.
Format: Article
Language:English
English
Published: American Society of Hematology 2018
Online Access:https://eprints.nottingham.ac.uk/52899/
_version_ 1848798835347816448
author Heery, David M.
author_facet Heery, David M.
author_sort Heery, David M.
building Nottingham Research Data Repository
collection Online Access
description Polycomb repressive complex 1 (PRC1) and PRC2 are transcriptional repressors that function as key regulators of the self-renewal and differentiation (cell lineage specification) pathways in stem cells. In this issue of Blood, Shima et al1 report that 2 ubiquitin ligases (Ring1A and Ring1B), which are key components of PRC1 complexes, are essential for the establishment and maintenance of acute myeloid leukemia (AML) in mouse models.
first_indexed 2025-11-14T20:26:05Z
format Article
id nottingham-52899
institution University of Nottingham Malaysia Campus
institution_category Local University
language English
English
last_indexed 2025-11-14T20:26:05Z
publishDate 2018
publisher American Society of Hematology
recordtype eprints
repository_type Digital Repository
spelling nottingham-528992019-04-19T04:30:27Z https://eprints.nottingham.ac.uk/52899/ A fellowship of Ring1 maintains AML stem cells Heery, David M. Polycomb repressive complex 1 (PRC1) and PRC2 are transcriptional repressors that function as key regulators of the self-renewal and differentiation (cell lineage specification) pathways in stem cells. In this issue of Blood, Shima et al1 report that 2 ubiquitin ligases (Ring1A and Ring1B), which are key components of PRC1 complexes, are essential for the establishment and maintenance of acute myeloid leukemia (AML) in mouse models. American Society of Hematology 2018-04-19 Article PeerReviewed application/pdf en https://eprints.nottingham.ac.uk/52899/1/A%20Fellowship%20of%20RING%20Proteins%20in%20AML%20Stem%20Cells.pdf image/tiff en https://eprints.nottingham.ac.uk/52899/7/Figure_v2.tif Heery, David M. (2018) A fellowship of Ring1 maintains AML stem cells. Blood, 131 (16). pp. 1771-1773. ISSN 1528-0020 http://dx.doi.org/10.1182/blood-2018-02-832121 doi:10.1182/blood-2018-02-832121 doi:10.1182/blood-2018-02-832121
spellingShingle Heery, David M.
A fellowship of Ring1 maintains AML stem cells
title A fellowship of Ring1 maintains AML stem cells
title_full A fellowship of Ring1 maintains AML stem cells
title_fullStr A fellowship of Ring1 maintains AML stem cells
title_full_unstemmed A fellowship of Ring1 maintains AML stem cells
title_short A fellowship of Ring1 maintains AML stem cells
title_sort fellowship of ring1 maintains aml stem cells
url https://eprints.nottingham.ac.uk/52899/
https://eprints.nottingham.ac.uk/52899/
https://eprints.nottingham.ac.uk/52899/