G-CSF receptor (CSF3R) mutations in X-linked neutropenia evolving to acute myeloid leukemia or myelodysplasia.
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Actin cytoskeletal defects in immunodeficiencyCongenital neutropenia: diagnosis, molecular bases and patient management.Inference of surface membrane factors of HIV-1 infection through functional interaction networks.Neutropenia in primary immunodeficiencySevere congenital neutropenia, a genetically heterogeneous disease group with an increased risk of AML/MDS.Dysplasia has A differential diagnosis: distinguishing genuine myelodysplastic syndromes (MDS) from mimics, imitators, copycats and impostors.A Truncated Granulocyte Colony-stimulating Factor Receptor (G-CSFR) Inhibits Apoptosis Induced by Neutrophil Elastase G185R Mutant: IMPLICATION FOR UNDERSTANDING CSF3R GENE MUTATIONS IN SEVERE CONGENITAL NEUTROPENIA.Case 2: Where have all the white cells gone?Molecular basis of congenital neutropenia.Incidence of severe congenital neutropenia in Sweden and risk of evolution to myelodysplastic syndrome/leukaemia
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G-CSF receptor (CSF3R) mutations in X-linked neutropenia evolving to acute myeloid leukemia or myelodysplasia.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on October 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
G-CSF receptor (CSF3R) mutatio ...... id leukemia or myelodysplasia.
@en
G-CSF receptor
@nl
type
label
G-CSF receptor (CSF3R) mutatio ...... id leukemia or myelodysplasia.
@en
G-CSF receptor
@nl
prefLabel
G-CSF receptor (CSF3R) mutatio ...... id leukemia or myelodysplasia.
@en
G-CSF receptor
@nl
P2860
P1433
P1476
G-CSF receptor (CSF3R) mutatio ...... oid leukemia or myelodysplasia
@en
P2093
Karolien Beel
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P304
P356
10.3324/HAEMATOL.2009.009001
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2009-10-01T00:00:00Z