The Clinical, Molecular, and Mechanistic Basis of RUNX1 Mutations Identified in Hematological Malign...
The Clinical, Molecular, and Mechanistic Basis of RUNX1 Mutations Identified in Hematological Malignancies
About this item
Full title
Author / Creator
Yokota, Asumi , Huo, Li , Lan, Fengli , Wu, Jianqiang and Huang, Gang
Publisher
Korean Society for Molecular and Cellular Biology
Journal title
Language
English
Formats
Publication information
Publisher
Korean Society for Molecular and Cellular Biology
Subjects
More information
Scope and Contents
Contents
RUNX1 plays an important role in the regulation of normal hematopoiesis.
RUNX1
mutations are frequently found and have been intensively studied in hematological malignancies. Germline mutations in
RUNX1
cause familial platelet disorder with predisposition to acute myeloid leukemia (FPD/AML). Somatic mutations of
RUNX1
are observed...
Alternative Titles
Full title
The Clinical, Molecular, and Mechanistic Basis of RUNX1 Mutations Identified in Hematological Malignancies
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_nrf_kci_oai_kci_go_kr_ARTI_6898275
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_nrf_kci_oai_kci_go_kr_ARTI_6898275
Other Identifiers
ISSN
1016-8478
E-ISSN
0219-1032
DOI
10.14348/molcells.2019.0252
