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Items: 1 to 20 of 103

  • The following term was not found in GEO DataSets: pachystachya.
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1.

Framework humanization increases the affinity and potency of anti-CD72 nanobody-based CAR-T cells for B-cell malignancies

(Submitter supplied) Anti-CD19 CAR T cells can induce remissions in some patients with B-cell malignancies. However, new immunotherapeutic targets are urgently needed for the many who relapse. We recently described CD72 as a promising target in B-cell leukemia and lymphoma, developing fully synthetic nanobody-based CAR-T cells (nanoCARs) against this antigen. Toward clinical translation, here we humanize our previous nanobody framework regions, derived from llama, and surprisingly discover a clone ("H24") with enhanced potency against B-cell tumors both in vitro and in vivo. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23227
18 Samples
Download data: TSV
Series
Accession:
GSE218791
ID:
200218791
2.

Transcriptomic changes induced by allosteric inhibitor RMC-4550 in FLT3 and KIT mutant human AML cell lines

(Submitter supplied) Targeting the MAPK signaling is an effective therapeutic approach in acute myeloid leukemia (AML) with mutations in FLT3 and KIT tyrosine kinase receptors. SHP2 is a central node in the MAPK signaling pathway and SHP2 inhibition was shown to supress leukemia proliferation in vitro and in vivo. In order to investigate the gene expression alterations induced by allosteric SHP2 inhibition and identify potential co-targets for pharmacological inhibition, we treated three human FLT3 and KIT mutant AML cell lines with RMC-4550 and performed RNAseq.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28038
18 Samples
Download data: TXT
Series
Accession:
GSE217359
ID:
200217359
3.

Transcriptomic analysis of HepG2 cells treated with BDE-47, BDE-99, BDE-209 and their ternary mixture at 1nM as a dietary relevant concentration

(Submitter supplied) Polybrominated diphenyl ethers (PBDEs) are persistent organic chemicals implied as flame re-tardants. Humans are mainly exposed to BDE-47, -99 and -209 congeners by diet. PBDEs are metabolic disruptors with liver as main target organ. To investigate their mode of action at a human relevant concentration, we exposed HepG2 cells to these congeners and their mixture at 1 nM for 72h, analyzing their transcriptomic and proteomic profiles. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10332
14 Samples
Download data: TXT
Series
Accession:
GSE216590
ID:
200216590
4.

Functional multi-omics reveals genetic and pharmacologic regulation of surface CD38 in multiple myeloma

(Submitter supplied) The goals of this study are to use multi-omics to design strategies to enhance efficacy of CD38-targeting immunotherapies in myeloma. We compared RNA-seq to cell surface proteomics after genetic and chemical manipulation of CD38 levels in myeloma cell lines.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23227
22 Samples
Download data: XLS
Series
Accession:
GSE181277
ID:
200181277
5.

Evolutionarily selected overexpression of the cytokine BAFF enhances mucosal immune response against P. falciparum

(Submitter supplied) A variant of the TNFSF13B gene (BAFF-var) increases the production of the cytokine BAFF, up-regulating humoral immunity and increasing the risk for certain autoimmune diseases. BAFF-var was evolutionarily advantageous, most likely by increasing resistance to malaria infection. We assessed experimentally the role of BAFF-var in response to malaria antigens. Lysates of erythrocytes infected with Plasmodium falciparum (iRBCs) or left uninfected (uRBCs, control) were used to treat PBMCs with distinct BAFF genotypes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
42 Samples
Download data: TXT
6.

Expression data from human foreskin fibroblast and human iduced pluripotent stem cell

(Submitter supplied) Pluripotent cells are important and unique because of unprecedently high proliferation and differentiation potentials. The state of pluripotency is robust enough to sustain years of uninterrupted proliferation in vitro, but, once lost, there is a significant barrier for differentiated cells to regain pluripotency. By now, reprogramming of somatic cells into a pluripotent state is unambiguously proven only for methods that necessarily involve ectopic expression or direct delivery of exogenous factors inside the cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
6 Samples
Download data: CEL, TXT
Series
Accession:
GSE135409
ID:
200135409
7.

KRASG12C inhibition produces a driver-limited state revealing collateral dependencies

(Submitter supplied) Inhibitors targeting KRASG12C, a mutant form of the guanosine triphosphatase (GTPase) KRAS, are a promising new class of oncogene-specific therapeutics for the treatment of tumors driven by the mutant protein. These molecules react with the mutant cysteine residue by binding covalently to the switch-II pocket (S-IIP) that is present only in the inactive guanosine diphosphate (GDP)-bound state of KRASG12C, sparing the wild-type protein. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
8 Samples
Download data: TXT
8.

Hypoxia is a Key Driver of Alternative Splicing in Human Breast Cancer Cells

(Submitter supplied) Adaptation to hypoxia, a hallmark feature of many tumors, is an important driver of cancer cell survival, proliferation and the development of resistance to chemotherapy. Hypoxia-induced stabilization of hypoxia-inducible factors (HIFs) leads to transcriptional activation of a network of hypoxia target genes involved in angiogenesis, cell growth, glycolysis, DNA damage repair and apoptosis. Although the transcriptional targets of hypoxia have been characterized, the alternative splicing of transcripts that occurs during hypoxia and the roles they play in oncogenesis are much less understood. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
3 Samples
Download data: BW
9.

Gene expression profiling of tumor cells and M2 macrophages from WT mice and mice with deletion of integrin beta3 in macrophage lineage cells (b3KOM)

(Submitter supplied) To better understand the impact of integrin beta3 signaling in myeloid cells on the tumor microenvironment, we compared the gene expression profiles of FACS isolated GFP+ PyMT-BO1 MFP tumor cells and also M2 TAMs (CD11b+Gr1-F4/80+CD206+) from tumor tissue of WT mice and b3ΚΟΜ mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
10 Samples
Download data: CEL, CHP, XLSX
Series
Accession:
GSE75882
ID:
200075882
10.

Role of the hypoxia-inducible histone H3K9 methylation regulating enzymes Jmjd1a and G9a in stem cell self-renewal and tumorigenesis

(Submitter supplied) Hypoxia is one of the major driving forces mediating tumor angiogenesis, aggressiveness, as well as resistance to chemo- and radiotherapy. It has also been suggested to play important roles in stem cell maintenance for both normal and cancer tissues. However, the mechanisms by which hypoxia-driven epigenetic changes modulate tumorigenesis remain poorly understood. As the histone H3 lysine 9 (H3K9) demethylase Jmjd1a and methyltransferase G9a are upregulated downstream targets of hypoxia, we focused on these two catalytically opposing epigenetic modifiers to address this question. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
63 Samples
Download data: TXT
Series
Accession:
GSE35061
ID:
200035061
11.

Isolation and characterization of progenitor-like cells from human renal proximal tubules

(Submitter supplied) The adult kidney has a remarkable capacity for self-renewal upon damage. Whether this regeneration is mediated by dedifferentiating surviving cells or as recently suggested by stem cells has not been unequivocally settled. The stem cell concept is however hampered by lack of consensus regarding the histological localization of and defining markers for these cells. Here, we demonstrate that aldehyde dehydrogenase (ALDH) activity may be used for isolation of cells with progenitor-like characteristics from adult human renal cortical tissue. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
6 Samples
Download data: TXT
Series
Accession:
GSE23911
ID:
200023911
12.

HepG2_MIX(biolrepl2)_Control(biolrepl2)

Organism:
Homo sapiens
Source name:
HepG2, MIX treatment 1nM, biolrepl2 (channel 1) HepG2, Control medium treatment, biolrepl2 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680998
ID:
306680998
13.

HepG2_MIX(biolrepl1)_Control(biolrepl1)

Organism:
Homo sapiens
Source name:
HepG2, MIX treatment 1nM, biolrepl1 (channel 1) HepG2, Control medium treatment, biolrepl1 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680997
ID:
306680997
14.

HepG2_BDE-99(biolrepl3)_Control(biolrepl3)

Organism:
Homo sapiens
Source name:
HepG2, BDE-209 treatment 1nM, biolrepl3 (channel 1) HepG2, Control medium treatment, biolrepl3 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680996
ID:
306680996
15.

HepG2_BDE-209(biolrepl3)_BDE-99(biolrepl3)

Organism:
Homo sapiens
Source name:
HepG2, BDE-209 treatment 1nM, biolrepl3 (channel 1) HepG2, BDE-99 treatment 1nM, biolrepl3 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680995
ID:
306680995
16.

HepG2_BDE-47(biolrepl3)_BDE-209(biolrepl3)

Organism:
Homo sapiens
Source name:
HepG2, BDE-47 treatment 1nM, biolrepl3 (channel 1) HepG2, BDE-209 treatment 1nM, biolrepl3 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680994
ID:
306680994
17.

HepG2_Control(biolrepl3)_BDE-47(biolrepl3)

Organism:
Homo sapiens
Source name:
HepG2, Control medium treatment, biolrepl3 (channel 1) HepG2, BDE-47 treatment 1nM, biolrepl3 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680993
ID:
306680993
18.

HepG2_BDE-209(biolrepl2)_MIX(biolrepl2)

Organism:
Homo sapiens
Source name:
HepG2, BDE-209 treatment 1nM, biolrepl2 (channel 1) HepG2, MIX treatment 1nM, biolrepl2 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680992
ID:
306680992
19.

HepG2_BDE-99(biolrepl2)_BDE-209(biolrepl2)

Organism:
Homo sapiens
Source name:
HepG2, BDE-99 treatment 1nM, biolrepl2 (channel 1) HepG2, BDE-209 treatment 1nM, biolrepl2 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680991
ID:
306680991
20.

HepG2_BDE-47(biolrepl2)_BDE-99(biolrepl2)

Organism:
Homo sapiens
Source name:
HepG2, BDE-47 treatment 1nM, biolrepl2 (channel 1) HepG2, BDE-99 treatment 1nM, biolrepl2 (channel 2)
Platform:
GPL10332
Series:
GSE216590
Download data: TXT
Sample
Accession:
GSM6680990
ID:
306680990
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db=gds|term=Stelis%20pachystachya|query=3|qty=3|blobid=MCID_670ab3c7475a635e85cc3f6b|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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