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TranscriptomicsRNA-seq expression profiling of NPM1mutated normal-AML with methylome status for HIST1 gene, i.e. H3K27me3 high (N=16) and H3K27me3 low (N=11). Transcriptome was done with Affymetrix HG-133+2.0 and Affymetrix Human Gene 2.0 ST microarrays
The epigenetic machinery is frequently altered in acute myeloid leukemia (AML). Focusing on cytogenetically normal (CN) AML, we previously described an abnormal H3K27me3 enrichment covering 70 kb on the HIST1 cluster (6.p22). Here, we further investigate the molecular, functional, and prognosis sign...
ORGANISM(S): Homo sapiens 
2020-08-25 | E-MTAB-6997 | biostudies-arrayexpress
UnknownStatistical Approach of the Role of the Conserved CSB-PiggyBac Transposase Fusion Protein (CSB-PGBD3) in Genotype-Phenotype Correlation in Cockayne Syndrome Type B.
Not available
S-EPMC8891132 | biostudies-literature
UnknownTwo Different PRKN Compound Heterozygous Variants Combinations in the Same Family.
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S-EPMC10187002 | biostudies-literature
UnknownDeep intronic variation in splicing regulatory element of the ERCC8 gene associated with severe but long-term survival Cockayne syndrome.
Not available
S-EPMC5891492 | biostudies-literature
UnknownSepax-2 cell processing device: a study assessing reproducibility of concentrating thawed hematopoietic progenitor cells.
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S-EPMC9632571 | biostudies-literature
Unknown4-Substituted 2-Hydroxyisoquinoline-1,3(2H,4H)-diones as a Novel Class of HIV-1 Integrase Inhibitors.
Not available
S-EPMC4027527 | biostudies-literature
UnknownHomology Model Versus X-ray Structure in Receptor-based Drug Design: A Retrospective Analysis with the Dopamine D3 Receptor.
Not available
S-EPMC4018084 | biostudies-literature
UnknownDefective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome.
Not available
S-EPMC6981198 | biostudies-literature
UnknownClinical and molecular overlap between nucleotide excision repair (NER) disorders and <i>DYRK1A</i> haploinsufficiency syndrome.
Not available
S-EPMC11979163 | biostudies-literature
UnknownIdentification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B.
Not available
S-EPMC8701866 | biostudies-literature
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