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Items: 1 to 20 of 42

1.

Lipid Associated Macrophages' Promotion of Fibrosis Resolution during MASH regression requires TREM2

(Submitter supplied) While macrophage heterogeneity during Metabolic dysfunction-associated steatohepatitis (MASH) has been described, the fate of these macrophages during MASH regression is poorly understood. Comparing macrophage heterogeneity during MASH progression vs regression, we identified specific macrophage sub- populations that are critical for MASH/fibrosis resolution. We elucidated the restorative pathways and gene signatures that define regression associated macrophages (RAM) and establish the importance of TREM2+ macrophages during MASH regression. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
9 Samples
Download data: RDS
Series
Accession:
GSE261829
ID:
200261829
2.

High-throughput Sequencing Facilitates Quantitative Analysis of Bone Marrow Macrophages and Spleenic Macrophages MicroRNA Expression in mouse MLL-AF9 acute myelogenous leukemia

(Submitter supplied) The goals of this study aim to reveal microRNA expression profiles of leukemia-associated macrophages and regulatory mechanism in response to the microenvironmental cues in mouse MLL-AF9 acute myelogenous leukemia
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE161292
ID:
200161292
3.

HIGHLY PHAGOCYTIC LIPID-ASSOCIATED MACROPHAGES (LAMs) ARE INCREASED 2 IN COLONIC LAMINA PROPRIA IN OBESITY

(Submitter supplied) Little is known about the effects of high fat diet (HFD)-induced obesity on resident colonic lamina propria (LP) macrophages (LPMs) function and metabolism. Here, we report that obesity and diabetes resulted in increased macrophage infiltration in the colon. These macrophages exhibited the residency phenotype CX3CR1hiMHCIIhi, and were CD4-TIM4-. During HFD, resident colonic LPM exhibited a lipid metabolism gene expression signature that overlapped that used to define lipid associated macrophages (LAMs). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21493
8 Samples
Download data: TSV
Series
Accession:
GSE240228
ID:
200240228
4.

Senataxin and RNase H2 act redundantly to suppress genome instability during class switch recombination

(Submitter supplied) Class switch recombination generates antibody distinct isotypes critical to a robust adaptive immune system and defects are associated with auto-immune disorders and lymphomagenesis. Transcription is required during class switch to recruit the cytidine deaminase AID—an essential step for the formation of DNA doublestrand breaks—and strongly induces the formation of R loops within the immunoglobulin heavy chain locus. more...
Organism:
Mus musculus
Type:
Other
Platforms:
GPL24247 GPL21103
24 Samples
Download data: BIGBED, BIGWIG, TXT
Series
Accession:
GSE201210
ID:
200201210
5.

Bulk RNAseq analysis reveals distinct differentiation traits of COMMD10-deficient Ly6Chi monocytes in the injured liver

(Submitter supplied) Hepatic macrophages play a central role in the initiation, progression and resolution of various liver diseases. Specifically, infiltrating Ly6Chi monocytes and their-derived macrophage (MoMFs) descendants prevail in acute or chronic liver injury, display marked transcriptional variance and provide crucial functional plasticity. A specific example of MoMFs are lipid associated macrophages (LAMs) involved in progression of metabolic liver disease (Remmerie et al., 2020). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
8 Samples
Download data: XLSX
Series
Accession:
GSE183494
ID:
200183494
6.

Single cell RNAseq reveals distinct differentiation traits of COMMD10-deficient Ly6Chi monocytes in the injured liver

(Submitter supplied) Hepatic macrophages play a central role in the initiation, progression and resolution of various liver diseases. Specifically, infiltrating Ly6Chi monocytes and their-derived macrophage (MoMFs) descendants prevail in acute or chronic liver injury, display marked transcriptional variance and provide crucial functional plasticity. A specific example of MoMFs are lipid associated macrophages (LAMs) involved in progression of metabolic liver disease (Remmerie et al., 2020). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
3 Samples
Download data: MTX, TSV
Series
Accession:
GSE183367
ID:
200183367
7.

GFI1 is pivotal for AML1-ETO positive acute myeloid leukemia

(Submitter supplied) AML1-ETO (Acute Myeloid Leukemia 1-Eight Twenty One) caused by the translocation t(8;21)(q22;q22) is a mutated transcription factor contributing to AML development. Although associated with a favorable prognosis, half of the patients fail to achieve long-term survival. We examined the role of the transcription factor Growth factor independence 1 (GFI1) in the initiation and progression of leukemia and exploited the use of a drug targeting GFI1 expression in the context of AML1-ETO associated AML. more...
Organism:
Homo sapiens; Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13112 GPL11154
3 Samples
Download data: WIG
Series
Accession:
GSE103255
ID:
200103255
8.

Next Generation Sequencing Facilitates Quantitative Analysis of Bone Marrow Macrophages and Splenic Macrophages Transcriptomes in Mouse MLL-AF9 AML Leukemia

(Submitter supplied) The goals of this study aim to reveal functional and phenotypic diversity of leukemia-associated macrophages in response to the microenvironmental cues in mouse MLL-AF9 AML leukemia
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: TXT
Series
Accession:
GSE72803
ID:
200072803
9.

Epigenetic therapy as a novel approach for GFI136N-associated AML

(Submitter supplied) Acute myeloid leukemia (AML) is characterized by accumulation of myeloid blast cells in the bone marrow. Despite all efforts, prognosis of AML patients remains poor, warranting new therapeutic approaches. A single nucleotide polymorphism of growth factor independence 1 (GFI1), a hematopoietic transcription factor, generates a protein with an asparagine (GFI136N) instead of a serine at position 36 (GFI136S), which we have previously reported to be associated with de novo AML in humans. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: XLSX
Series
Accession:
GSE77073
ID:
200077073
10.

Effect of Gfi1 36N variant on genome-wide H3K9 Acetylation patterns

(Submitter supplied) ChIP-Seq Analysis of H3K9Ac in pairs of mouse and human samples carrying either the Gfi136S or the GFi136N variants. The objective of the study was to identify the changes in H3K9 acetylation at gene promoters that occur in samples expressing the 36N variant of the Gfi1 gene.
Organism:
Mus musculus; Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9250 GPL11154 GPL13112
24 Samples
Download data: TXT
Series
Accession:
GSE71254
ID:
200071254
11.

Gfi1 as a new predictive and therapeutical target of MDS/AML

(Submitter supplied) MDS is characterized by a disturbed function of the myeloid lineage of the hematopoietic system that may transform to AML, a malignant disease of the myeloid compartment. Epigenetic and genetic aberrations contribute to the initiation and progression of MDS/AML. GFI1 is a transcriptional repressor, which regulates expression of its target genes by, among other approaches, recruiting HDACs to its target genes to remove histone 3 lysine 9 (H3K9) acetylation, a marker for active gene expression. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT
Series
Accession:
GSE72671
ID:
200072671
12.

Next Generation Sequencing Facilitates Quantitative Analysis of Bone Marrow Macrophages and Spleenic Macrophages Transcriptomes in mouse T cell acute lymphoblastic leukemia

(Submitter supplied) The goals of this study aim to reveal functional and phenotypic diversity of leukemia-associated macrophages in response to the microenvironmental cues in mouse T cell acute lymphoblastic leukemia
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE63751
ID:
200063751
13.

Gene Expression in Rats Fed a Western Diet

(Submitter supplied) Resistant starches (RS), fed as high amylose maize starch (HAMS) or butyrylated HAMS (HAMSB), oppose dietary protein-induced colonocyte DNA damage in rats. In this study, rats were fed diets high in fat (19%) and protein (20%) with different forms of digestible starch (low amylose maize starch (LAMS) or low amylose whole wheat (LAW)) or RS (HAMS, HAMSB, or a whole high amylose wheat (HAW) generated by RNA interference (RNAi)) for 11 wk. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6247
43 Samples
Download data: CEL
Series
Accession:
GSE32312
ID:
200032312
14.

Macrophages form 18Day AML Spleen

Organism:
Mus musculus
Source name:
Macrophage
Platform:
GPL17021
Series:
GSE161292
Download data
Sample
Accession:
GSM4904383
ID:
304904383
15.

Macrophages form 18Day AML BM

Organism:
Mus musculus
Source name:
Macrophage
Platform:
GPL17021
Series:
GSE161292
Download data
Sample
Accession:
GSM4904382
ID:
304904382
16.

LAMS HTGTS-seq WT cut biol rep 2

Organism:
Mus musculus
Source name:
Spleen
Platform:
GPL24247
Series:
GSE201210
Download data: TXT
Sample
Accession:
GSM6052744
ID:
306052744
17.

LAMS HTGTS-seq setx-/- cut biol rep 2

Organism:
Mus musculus
Source name:
Spleen
Platform:
GPL24247
Series:
GSE201210
Download data: TXT
Sample
Accession:
GSM6052743
ID:
306052743
18.

LAMS HTGTS-seq rnaseh2b-/- cut biol rep 2

Organism:
Mus musculus
Source name:
Spleen
Platform:
GPL24247
Series:
GSE201210
Download data: TXT
Sample
Accession:
GSM6052742
ID:
306052742
19.

LAMS HTGTS-seq rnaseh2b-/- setx-/- cut biol rep 2

Organism:
Mus musculus
Source name:
Spleen
Platform:
GPL24247
Series:
GSE201210
Download data: TXT
Sample
Accession:
GSM6052741
ID:
306052741
20.

LAMS HTGTS-seq WT cut biol rep 1

Organism:
Mus musculus
Source name:
Spleen
Platform:
GPL24247
Series:
GSE201210
Download data: TXT
Sample
Accession:
GSM6052740
ID:
306052740
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db=gds|term=LAMS|query=1|qty=4|blobid=MCID_67252c79ffa1095b204c384a|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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