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Displaying 20 of 74 results for "ASXL1"
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  1. Loss of Asxl1 Alters Self-Renewal and Cell Fate of Bone Marrow Stromal Cell BioProject

    ID: PRJNA305430

    Keywords: Transcriptome or Gene expression

    Access Type: download

  2. ASXL1 Interacts with the Cohesin Complex to Maintain Chromatid Separation and Gene Expression for Normal Hematopoiesis [RNA-Seq] BioProject

    ID: PRJNA327564

    Keywords: Transcriptome or Gene expression

    Access Type: download

  3. Cancer-associated ASXL1 mutations may act as gain-of-function mutations of the ASXL1-BAP1 complex BioProject

    ID: PRJNA274361

    Keywords: Other

    Access Type: download

  4. ASXL1 Knock Down in Normal CD34+ Cord Blood and UKE1 Cell Lines BioProject

    ID: PRJNA168443

    Keywords: Transcriptome or Gene expression

    Access Type: download

  5. Cancer-associated ASXL1 mutations may act as gain-of-function mutations of the ASXL1-BAP1 complex OmicsDI

    ID: E-GEOD-65555

    Date Released: 03-21-2015

    Description: ASXL1 is the obligate regulatory subunit of a deubiquitinase complex whose catalytic subunit is BAP1. Heterozygous mutations of

  6. Cancer-associated ASXL1 mutations may act as gain-of-function mutations of the ASXL1-BAP1 complex ArrayExpress

    ID: E-GEOD-65555

    Description: ASXL1 is the obligate regulatory subunit of a deubiquitinase complex whose catalytic subunit is BAP1. Heterozygous mutations of

  7. Mus musculus strain:C57BL/6 : Collaborative effects of SETBP1-D868N with ASXL1-MT in inducing AML BioProject

    ID: PRJDB3156

    Keywords: Transcriptome or Gene expression

    Access Type: download

  8. ASXL1 Mutations Promote Myeloid Transformation Through Loss of PRC2-Mediated Gene Repression BioProject

    ID: PRJNA169078

    Keywords: Epigenomics

    Access Type: download

  9. Loss of Asxl1 Alters Mesenchymal Stem Cell Fate through H3K4me3 BioProject

    ID: PRJNA305426

    Access Type: download

  10. Loss of Asxl1 Alters Self-Renewal and Cell Fate of Bone Marrow Stromal Cell ArrayExpress

    ID: E-GEOD-75787

    Description: De novo ASXL1 mutations are found in patients with Bohring-Opitz syndrome, a disease with severe developmental defects and early childhood ...

  11. ASXL1 Interacts with the Cohesin Complex to Maintain Chromatid Separation and Gene Expression for Normal Hematopoiesis [ChIP-Seq] BioProject

    ID: PRJNA327562

    Keywords: Epigenomics

    Access Type: download

  12. ASXL1 Mutations Promote Myeloid Transformation Through Loss of PRC2-Mediated Gene Repression ArrayExpress

    ID: E-GEOD-38861

    Description: Recurrent somatic ASXL1 mutations occur in patients with myelodysplasia (MDS), myeloproliferative neoplasms (MPN), and acute myeloid leukemia (AML), ...

  13. Chromatin maps of human ASXL1, FOXK1 and O-GlcNAc BioProject

    ID: PRJNA224307

    Keywords: Epigenomics

    Access Type: download

  14. Transcription profiling by array of human UKE-1 cells with shRNA mediated knock-down of ASXL1 ArrayExpress

    ID: E-GEOD-38692

    Description: d UKE1 cell lines treated with hairpins targeting ASXL1. Two independent studies where 1) CD34+ cord blood from normal donors were treated with either A) GFP Vector or B) ASXL1 specific short hairp...

  15. Loss of Asxl1 Alters Mesenchymal Stem Cell Fate through H3K4me3 ArrayExpress

    ID: E-GEOD-75788

    Description: This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

  16. Loss of Asxl1 Alters Self-Renewal and Cell Fate of Bone Marrow Stromal Cell OmicsDI

    ID: E-GEOD-75787

    Date Released: 06-30-2016

    Description: De novo ASXL1 mutations are found in patients with Bohring-Opitz syndrome, a disease with severe developmental defects and early childhood ...

  17. ASXL1 Mutations Promote Myeloid Transformation Through Loss of PRC2-Mediated Gene Repression OmicsDI

    ID: E-GEOD-38861

    Date Released: 09-26-2012

    Description: Recurrent somatic ASXL1 mutations occur in patients with myelodysplasia (MDS), myeloproliferative neoplasms (MPN), and acute myeloid leukemia (AML), ...

  18. Expression analysis of 32Dcl3 cells expressing ASXL-MT in the presence of IL-3 or G-CSF ArrayExpress

    ID: E-GEOD-49117

    Description: Recurrent mutations in ASXL1 are found in various hematological malignancies and are associated with poor prognosis. In particular, ASXL1

  19. Chromatin maps of human ASXL1, FOXK1 and O-GlcNAc ArrayExpress

    ID: E-GEOD-51673

    Description: ide chromatin maps of identified PR-DUB1 subunits ASXL1, FOXK1 and the OGT1 catalyzed modification O-GlcNAc based on ChIP-seq. Our data set comprises 3 ChIP-seq samples plus 2 input control samples using chromatin from Flp-In HEK293 T-REx cells cells which was immunoprecipitated using antibodies against ASXL1, FOXK1 and O-GlcNAc....

  20. Transcription profiling by array of patients with ASXL1 mutations in cytogenetically normal acute myeloid leukemia ArrayExpress

    ID: E-TABM-1208

    Description: wild-type NPM1 and no FLT3-ITD. We identified an ASXL1 mutation-associated gene expression signature by comparing 26 ASXL1-mutated and 39 ASXL1-wild type patients. Only NPM1 wild type/FLT3-ITD-negative patients were inc...


Displaying 20 of 74 results for "ASXL1"