Related references
Note: Only part of the references are listed.Gatekeeper function of the RUNX1 transcription factor in acute leukemia
Birte Niebuhr et al.
BLOOD CELLS MOLECULES AND DISEASES (2008)
Amplification at 7q22 targets cyclin-dependent kinase 6 in T-cell lymphoma
S. Nagel et al.
LEUKEMIA (2008)
Integrated profiling of basal and luminal breast cancers
Jose Adelaide et al.
CANCER RESEARCH (2007)
Gene expression profiling separates chronic myelomonocytic leukemia in two molecular subtypes
V. Gelsi-Boyer et al.
LEUKEMIA (2007)
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype
Hilde Brems et al.
NATURE GENETICS (2007)
Germline gain-of-function mutations in RAF1 cause Noonan syndrome
M. Abdur Razzaque et al.
NATURE GENETICS (2007)
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
Bhaswati Pandit et al.
NATURE GENETICS (2007)
Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11
C. Flotho et al.
ONCOGENE (2007)
Chronic myelomonocytic leukemia in the light of the WHO proposals
Ulrich Germing et al.
HAEMATOLOGICA (2007)
Rearrangements involving 12q in myeloproliferative disorders:: possible role of HMGA2 and SOCS2 genes
Anne Etienne et al.
CANCER GENETICS AND CYTOGENETICS (2007)
Targeting RAS signaling pathways in juvenile myelomonocytic leukemia
Christian Flotho et al.
CURRENT DRUG TARGETS (2007)
Mutations of the PTPNII gene in therapy-related MDS and AML with rare balanced chromosome translocations
Debes H. Christiansen et al.
GENES CHROMOSOMES & CANCER (2007)
Cdk6 blocks myeloid differentiation by interfering with Runx1 DNA binding and Runx1-C/EBPα interaction
T. Fujimoto et al.
EMBO JOURNAL (2007)
Neurofibromatosis 1
Rosalie E. Ferner
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
Germline gain-of-function mutations in SOS1 cause Noonan syndrome
Amy E. Roberts et al.
NATURE GENETICS (2007)
Hyperactive Ras in developmental disorders and cancer
Suzanne Schubbert et al.
NATURE REVIEWS CANCER (2007)
The impact of translocations and gene fusions on cancer causation
Felix Mitelman et al.
NATURE REVIEWS CANCER (2007)
AML1/Runx1 as a versatile regulator of hematopoiesis: Regulation of its function and a role in adult hematopoiesis
Mineo Kurokawa
INTERNATIONAL JOURNAL OF HEMATOLOGY (2006)
Recurrent KRAS Codon 146 mutations in human colorectal cancer
Sarah Edkins et al.
CANCER BIOLOGY & THERAPY (2006)
Inherited predispositions and hyperactive Ras in myeloid leukemogenesis
JO Lauchle et al.
PEDIATRIC BLOOD & CANCER (2006)
The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease
CP Kratz et al.
BLOOD (2005)
Acquired PTPN11 mutations occur rarely in adult patients with myelodysplastic syndromes and chronic myelomonocytic leukemia
ML Loh et al.
LEUKEMIA RESEARCH (2005)
HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;p11.2)
C Morerio et al.
CANCER RESEARCH (2004)
Endogenous oncogenic K-rasG12D stimulates proliferation and widespread neoplastic and developmental defects
DA Tuveson et al.
CANCER CELL (2004)
Somatic activation of oncogenic Kras in hematopoietic cells initiates a rapidly fatal myeloproliferative disorder
BS Braun et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA
MT Barrett et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Activating mutations of the Noonan syndrome-associated SHP2/PTPN11 gene in human solid tumors and adult acute myelogenous leukemia
M Bentires-Alj et al.
CANCER RESEARCH (2004)
AML1/Runx1 recruits calcineurin to regulate granulocyte macrophage colony-stimulating factor by Ets1 activation
HB Liu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Point mutations in the RUNX1/AML1 gene:: another actor in RUNX leukemia
M Osato
ONCOGENE (2004)
Breakpoints at 1p36.3 in three MDS/AML(M4) patients with t(1;3)(p36;q21) occur in the first intron and in the 5′ region of MEL1
PT Xinh et al.
GENES CHROMOSOMES & CANCER (2003)
The World Health Organization (WHO) classification of the myeloid neoplasms
JW Vardiman et al.
BLOOD (2002)
Two groups of chronic myelomonocytic leukaemia:: myelodysplastic and myeloproliferative.: Prognostic implications in a series of a single center
I González-Medina et al.
LEUKEMIA RESEARCH (2002)
Prognostic factors and scoring systems in chronic myelomonocytic leukemia: a retrospective analysis of 213 patients
F Onida et al.
BLOOD (2002)
Dysplastic versus proliferative CMML -: a retrospective analysis of 91 patients from a single institution
T Nösslinger et al.
LEUKEMIA RESEARCH (2001)
Share Paper
