X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (21) 21
index medicus (19) 19
hematology (16) 16
leukemia, myeloid, acute - genetics (16) 16
female (15) 15
male (15) 15
middle aged (14) 14
adult (13) 13
adolescent (12) 12
prognosis (9) 9
young adult (9) 9
cancer (8) 8
mutation (8) 8
oncology (8) 8
abridged index medicus (7) 7
aged (6) 6
treatment outcome (6) 6
younger adults (6) 6
acute myeloid leukemia (5) 5
cohort studies (5) 5
diagnosis (5) 5
fms-like tyrosine kinase 3 - genetics (5) 5
leukemia, myeloid, acute - drug therapy (5) 5
mutation - genetics (5) 5
prognostic-significance (5) 5
survival rate (5) 5
austria (4) 4
colony-stimulating factor (4) 4
germany (4) 4
group-b (4) 4
leukemia, myeloid, acute - mortality (4) 4
leukemia, myeloid, acute - therapy (4) 4
mutations (4) 4
nuclear proteins - genetics (4) 4
trial (4) 4
acute myelogenous leukemia (3) 3
aged, 80 and over (3) 3
aml (3) 3
biomarkers, tumor - genetics (3) 3
ccaat-enhancer-binding proteins - genetics (3) 3
dna mutational analysis (3) 3
gene mutations (3) 3
genetic aspects (3) 3
kaplan-meier estimate (3) 3
leukemia (3) 3
leukemia, myeloid, acute - classification (3) 3
normal cytogenetics (3) 3
normal karyotype (3) 3
nucleophosmin npm1 (3) 3
oligonucleotide array sequence analysis (3) 3
pediatrics (3) 3
polymerase-chain-reaction (3) 3
recurrence (3) 3
study-group ulm (3) 3
acute myeloid-leukemia (2) 2
acute promyelocytic leukemia (2) 2
adults (2) 2
antineoplastic combined chemotherapy protocols - therapeutic use (2) 2
article (2) 2
bone marrow (2) 2
ccaat-enhancer-binding protein-alpha - genetics (2) 2
cebpa mutations (2) 2
cells, cultured (2) 2
chromosome aberrations (2) 2
chromosome inversion (2) 2
chromosomes, human, pair 8 (2) 2
core binding factors - genetics (2) 2
cytogenetic analysis (2) 2
cytogenetics (2) 2
disease-free survival (2) 2
drug resistance, neoplasm - genetics (2) 2
endothelium, vascular - metabolism (2) 2
favorable prognosis (2) 2
gene expression (2) 2
gene expression profiling (2) 2
gene expression profiling - methods (2) 2
genotype (2) 2
health aspects (2) 2
hemic and lymphatic diseases (2) 2
imaging (2) 2
infant (2) 2
interleukin-1 (2) 2
internal tandem duplication (2) 2
leukemia, myeloid, acute - pathology (2) 2
multidisciplinary sciences (2) 2
mutation - physiology (2) 2
myelodysplastic syndrome (2) 2
myelodysplastic syndromes (2) 2
myeloid leukemia (2) 2
myeloid-lymphoid leukemia protein - genetics (2) 2
polymerase chain reaction (2) 2
poor-prognosis (2) 2
prospective studies (2) 2
proto-oncogene proteins c-kit - genetics (2) 2
remission induction (2) 2
research (2) 2
risk factors (2) 2
science (2) 2
sensitivity and specificity (2) 2
stem-cells (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Clinical Oncology, ISSN 0732-183X, 04/2011, Volume 29, Issue 10, pp. 1364 - 1372
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 05/2008, Volume 358, Issue 18, pp. 1909 - 1918
Journal Article
Journal Article
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 05/2019, Volume 10, Issue 1, pp. 2031 - 11
Mutations in the nucleophosmin 1 (NPM1) gene are considered founder mutations in the pathogenesis of acute myeloid leukemia (AML). To characterize the genetic... 
AML | STEM-CELLS | HEMATOPOIESIS | MULTIDISCIPLINARY SCIENCES | DNMT3A | GENE-EXPRESSION | NORMAL CYTOGENETICS | PROGNOSTIC-SIGNIFICANCE | MINIMAL RESIDUAL DISEASE | YOUNGER ADULT PATIENTS | SOMATIC MUTATIONS | Myeloid leukemia | Pathogenesis | Leukemia | Mutation | Diagnosis | Ribonucleic acid--RNA | Acute myeloid leukemia | Gene sequencing
Journal Article
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 1207 - 1207
Abstract Background: Acute myeloid leukemia (AML) with t(8;21)(q22;q22) results in the formation of the RUNX1-RUNX1T1 fusion transcript which can be used to... 
Journal Article
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 3818 - 3818
Abstract Background: The ASXL2 (Additional Sex comb-like 2) gene on chromosome 2p23.3 encodes an epigenetic regulator that is thought to act through histone... 
Journal Article
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 226 - 226
Abstract Background: The DNA methyltransferase 3A (DNMT3A) is one of the most frequent mutated genes in AML with a hot spot mutation at codon R882 in 80% of... 
Journal Article
Nature genetics, ISSN 1061-4036, 09/2010, Volume 42, Issue 9, pp. 794 - 800
Journal Article
Blood, ISSN 0006-4971, 01/2013, Volume 121, Issue 1, pp. 170 - 177
Journal Article
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 227 - 227
Abstract Background: Nucleophosmin (NPM1mut) mutations represent one of the most common gene mutations in acute myeloid leukaemia (AML) and can be used for... 
Journal Article