Sort   by:  
 Page size 
UnknownRandomized open-label phase II study of decitabine in patients with low- or intermediate-risk myelodysplastic syndromes.
Not available
S-EPMC4878053 | biostudies-literature
ModelsGiantsosAdams2013 - Growth of glycocalyx under static conditions
Giantsos-Adams2013 - Growth of glycocalyx under static conditions This model is described in the article: Heparan Sulfate Regrowth Profiles Under Laminar Shear Flow Following Enzymatic Degradation. Giantsos-Adams KM, Koo AJ, Song...
2024-09-02 | BIOMD0000000830 | BioModels
ModelsGiantsos-Adams2013 - Growth of glycocalyx under static conditions
Giantsos-Adams2013 - Growth of glycocalyx under static conditions This model is described in the article: Heparan Sulfate Regrowth Profiles Under Laminar Shear Flow Following Enzymatic Degradation. Giantsos-Adams KM, Koo AJ, Song S, Sakai J, Sankaran J, Shin JH, Garcia-Carde...
2016-09-28 | MODEL1609100001 | BioModels
UnknownPhase I study of oral azacitidine in myelodysplastic syndromes, chronic myelomonocytic leukemia, and acute myeloid leukemia.
Not available
S-EPMC3675699 | biostudies-literature
UnknownValidation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes.
Not available
S-EPMC3438234 | biostudies-literature
ProteomicsHigh mobility group protein-mediated transcription requires DNA damage marker γ-H2AX
The eukaryotic genome is organized into chromatins, the physiological template for DNA-dependent processes including replication, recombination, repair, and transcription. Chromatin-mediated transcription regulation involves DNA methylation, chromatin remodeling, and histone modifications. However, ...
ORGANISM(S): Mus musculus (Mouse) 
2020-12-15 | PXD016586 | Pride
R-loops H2a.x Hmga2 Dna demethylation Tgfb1 Fact 
UnknownClearance of Somatic Mutations at Remission and the Risk of Relapse in Acute Myeloid Leukemia.
Not available
S-EPMC6008108 | biostudies-literature
TranscriptomicsDetection of chromothripsis-like patterns from custom array platform for chronic lymphocytic leukemia diagnosis (qchip Hemo custom array v3)
Chronic lymphocytic leukemia (CLL) is the most frequent leukemia in Western countries. The main genetic alterations associated to this disease are loss of 13q14, loss of 11q23, trisomy 12 and, less frequently, 17p13 losses, and are routinely studied using fluorescence in situ hybridization. These ge...
ORGANISM(S): Homo sapiens 
2015-08-31 | E-GEOD-66922 | biostudies-arrayexpress
UnknownMyroides species, pathogenic spectrum and clinical microbiology sight in Mexican isolates.
Not available
S-EPMC11534234 | biostudies-literature
TranscriptomicsCCND2 rearrangements are the most frequent genetic events in Cyclin D1-negative mantle cell lymphoma [Agilent]
Cyclin D1-negative mantle cell lymphomas (MCL) are not well characterized, in part due to the difficulties in their recognition. SOX11 has been recently identified as a reliable biomarker of MCL, also expressed in the cyclin D1-negative variant. We investigated 40 lymphomas with MCL morphology and i...
ORGANISM(S): Homo sapiens 
2012-12-19 | E-GEOD-42917 | biostudies-arrayexpress
Sort   by:  
 Page size