Related references
Note: Only part of the references are listed.Spontaneous abrogation of the G(2) DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients
Raphael Ceccaldi et al.
JOURNAL OF CLINICAL INVESTIGATION (2011)
Diagnosis of Myelodysplastic Syndrome Among a Cohort of 119 Patients With Fanconi Anemia Morphologic and Cytogenetic Characteristics
Adina M. Cioc et al.
AMERICAN JOURNAL OF CLINICAL PATHOLOGY (2010)
Genetic deletions in AML and MDS
Benjamin L. Ebert
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY (2010)
Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasms
Nils H. Thoennissen et al.
BLOOD (2010)
Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies
Christine O'Keefe et al.
BLOOD (2010)
Pathophysiology and management of inherited bone marrow failure syndromes
Akiko Shimamura et al.
BLOOD REVIEWS (2010)
Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia
Benoite Perez et al.
BRITISH JOURNAL OF HAEMATOLOGY (2010)
Clinical, Molecular, and Prognostic Significance of WHO Type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and Various Other 3q Abnormalities in Acute Myeloid Leukemia
Sanne Lugthart et al.
JOURNAL OF CLINICAL ONCOLOGY (2010)
Mutation analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 patients with MDS or secondary AML
F. Dicker et al.
LEUKEMIA (2010)
Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes
Gorica Nikoloski et al.
NATURE GENETICS (2010)
Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia
Maria Kleppe et al.
NATURE GENETICS (2010)
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
Thomas Ernst et al.
NATURE GENETICS (2010)
How the Fanconi Anemia Pathway Guards the Genome
George-Lucian Moldovan et al.
ANNUAL REVIEW OF GENETICS (2009)
The favorable impact of CEBPA mutations in patients with acute myeloid leukemia is only observed in the absence of associated cytogenetic abnormalities and FLT3 internal duplication
Aline Renneville et al.
BLOOD (2009)
Diagnosis of Fanconi anemia in patients with bone marrow failure
Fernando O. Pinto et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2009)
Myelodysplasia and Acute Leukemia as Late Complications of Marrow Failure: Future Prospects for Leukemia Prevention
Grover C. Bagby et al.
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA (2009)
The genetic and molecular basis of Fanconi anemia
Johan P. de Winter et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2009)
Finding the needle in the hay stack: Hematopoietic stem cells in Fanconi anemia
Lars U. W. Mueller et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2009)
Fanconi anemia and its diagnosis
Arleen D. Auerbach
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2009)
Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms
Masashi Sanada et al.
NATURE (2009)
Whole genome scanning as a cytogenetic tool in hematologic malignancies
Jaroslaw P. Maciejewski et al.
BLOOD (2008)
Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia
C. T. Storlazzi et al.
BLOOD CELLS MOLECULES AND DISEASES (2008)
Mutations of the TP53 gene in acute myeloid leukemia are strongly associated with a complex aberrant karyotype
C. Haferlach et al.
LEUKEMIA (2008)
Cooperating gene mutations in acute myeloid leukemia: a review of the literature
A. Renneville et al.
LEUKEMIA (2008)
Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia
Richard F. Schlenk et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Deregulation of signaling pathways in acute myeloid leukemia
Claudia Scholl et al.
SEMINARS IN ONCOLOGY (2008)
Hematopoietic stem cell transplantation in childhood inherited bone marrow failure syndrome
E. Gluckman et al.
BONE MARROW TRANSPLANTATION (2008)
Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes
Azim Mohamedali et al.
BLOOD (2007)
TNF-α induces leukemic clonal evolution ex vivo in Fanconi anemia group C murine stem cells
June Li et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children
Emmanuelle Clappier et al.
BLOOD (2007)
Amplification and translocation of 3q26 with overexpression of EVII in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD/BRCA2 disruption
Stefan Meyer et al.
GENES CHROMOSOMES & CANCER (2007)
Overexpression of PRDM16 in the presence and absence of the RUNX1/PRDM16 fusion gene in myeloid leukemias
Sawcene Hazourli et al.
GENES CHROMOSOMES & CANCER (2006)
Identification of truncated RUNX1 and RUNX1-PRDM16 fusion transcripts in a case of t(1;21)(p36;q22)-positive therapy-related AML
MJPL Stevens-Kroef et al.
LEUKEMIA (2006)
Ex vivo culture of Fancc-/- stem/progenitor cells predisposes cells to undergo apoptosis, and surviving stem/progenitor cells display cytogenetic abnormalities and an increased risk of malignancy
XX Li et al.
BLOOD (2005)
Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway
J Soulier et al.
BLOOD (2005)
Human fanconi anemia monoubiquitination pathway promotes homologous DNA repair
K Nakanishi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
The Fanconi anaemia gene FANCC promotes homologous recombination and error-prone DNA repair
W Niedzwiedz et al.
MOLECULAR CELL (2004)
Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients:: gains of the chromosomal segment 3q26q29 as an adverse risk factor
H Tönnies et al.
BLOOD (2003)
A 20-year perspective on the International Fanconi Anemia Registry (IFAR)
DI Kutler et al.
BLOOD (2003)
Distinct clinical outcomes for cytogenetic abnormalities evolving from aplastic anemia
JP Maciejewski et al.
BLOOD (2002)
Fanconi anemia: Myelodysplasia as a predictor of outcome
BP Alter et al.
CANCER GENETICS AND CYTOGENETICS (2000)
Share Paper
