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Accession: PRJNA472052 ID: 472052

Epigenetic drugs selectively target a population of AML cells which are positive for CD123 cell surface markers and are chemoresistant

This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series
AccessionPRJNA472052; GEO: GSE114649
TypeUmbrella project
Publications
  • Yan B et al., "Low-frequency TP53 hotspot mutation contributes to chemoresistance through clonal expansion in acute myeloid leukemia.", Leukemia, 2020 Jul;34(7):1816-1827
  • Yan B et al., "Histone deacetylase inhibitor targets CD123/CD47-positive cells and reverse chemoresistance phenotype in acute myeloid leukemia.", Leukemia, 2019 Apr;33(4):931-944
SubmissionRegistration date: 18-May-2018
University of Florida
RelevanceSuperseries
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments6
Publications
PubMed2
PMC1
Other datasets
BioSample6
GEO DataSets3
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes3
SRA Data Details
ParameterValue
Data volume, Gbases46
Data volume, Mbytes19880
Epigenetic drugs selectively target a population of AML cells which are positive for CD123 cell surface markers and are chemoresistant encompasses the following 2 sub-projects:
Project TypeNumber of Projects
Transcriptome or Gene expression2
BioProject
accession
OrganismTitle
PRJNA472053Homo sapiensEpigenetic drugs selectively target a population of AML cells which are positive for CD123 cell surface markers and are chemoresistant II (University of Florida)
PRJNA422583Homo sapiensEpigenetic drugs selectively target a population of AML cells which are positive for CD123 cell surface markers and are chemoresistant I (University of Florida)

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