Abrogation of RUNX1 gene expression in de novo myelodysplastic syndrome with t(4;21)(q21;q22).
about
A neonate with congenital amegakaryocytic thrombocytopenia associated with a chromosomal microdeletion at 21q22.11 including the gene RUNX1.Review of therapeutic options and the management of patients with myelodysplastic syndromes.Genetics and Epigenetics of Myelodysplastic Syndromes and Response to Drug Therapy: New Insights.Regulation of RUNX1 dosage is crucial for efficient blood formation from hemogenic endothelium.
P2860
Abrogation of RUNX1 gene expression in de novo myelodysplastic syndrome with t(4;21)(q21;q22).
description
2011 nî lūn-bûn
@nan
2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Abrogation of RUNX1 gene expre ...... yndrome with t(4;21)(q21;q22).
@ast
Abrogation of RUNX1 gene expre ...... yndrome with t(4;21)(q21;q22).
@en
type
label
Abrogation of RUNX1 gene expre ...... yndrome with t(4;21)(q21;q22).
@ast
Abrogation of RUNX1 gene expre ...... yndrome with t(4;21)(q21;q22).
@en
prefLabel
Abrogation of RUNX1 gene expre ...... yndrome with t(4;21)(q21;q22).
@ast
Abrogation of RUNX1 gene expre ...... yndrome with t(4;21)(q21;q22).
@en
P2093
P2860
P50
P1433
P1476
Abrogation of RUNX1 gene expre ...... yndrome with t(4;21)(q21;q22).
@en
P2093
Ana Rio-Machín
Bibiana I Ferreira
Francesco Acquadro
Juan C Cigudosa
Karmele A Juaristi
Sara Alvarez
P2860
P304
P356
10.3324/HAEMATOL.2011.050567
P577
2011-11-18T00:00:00Z