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Items: 1 to 20 of 890

  • The following term was not found in GEO DataSets: laetum.
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  • Showing results for avium laetum. Search instead for Apium laetum (0)
1.

Gene expression profile of human monocyte-derived macrophage stimulated with AGP, anti-CD74 antibody, and mycobacterium avium infaction

(Submitter supplied) Macrophages are immune cells inctributing to several kinds of diseases, and activation status of macrophages are considered to be regulated by several stimulations. To test the gene expression change in activated macrophages, human monocyte-derived macrophages were stimulated with alpha1-acid glycoprotein (AGP), anti-CD74 blocking antobody, anti-CD74-agonistic antibody. Macrophages infected with Micobacterium avium were also tested. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: TXT
Series
Accession:
GSE217996
ID:
200217996
2.

The detection of Prunus virus F and its distribution in Hungarian sour cherry orchards

(Submitter supplied) Viromes of sour and sweet cherry trees in Hungarian germ line collections were surveyed using small RNA HTS as an unbiased method. RNA from leaf samples of different cultivars were purified and used to produce seven pools from which small RNA HTS libraries were prepared. The sequenced reads were analyzed using bioinformatic methods to revel the presence of viruses in the samples. Presence of the viruses were validated using RT-PCR.
Organism:
Prunus avium; Prunus cerasus
Type:
Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL33434 GPL23007
7 Samples
Download data: TXT
Series
Accession:
GSE233558
ID:
200233558
3.

Gene expression profile of human monocyte-derived macrophage stimulated with AGP, anti-CD74 antibody, CRP, and mycobacterium avium infaction.

(Submitter supplied) Macrophages are immune cells inctributing to several kinds of diseases, and activation status of macrophages are considered to be regulated by several stimulations. To test the gene expression change in activated macrophages, human monocyte-derived macrophages were stimulated with alpha1-acid glycoprotein (AGP), anti-CD74 blocking antobody, anti-CD74-agonistic antibody. Macrophages infected with Micobacterium avium were also tested. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
8 Samples
Download data: TXT
Series
Accession:
GSE237240
ID:
200237240
4.

Comparative transcriptomic profiling between two radiologic phenotypes in lungs from patients with pulmonary disease caused by Mycobacterium avium complex

(Submitter supplied) The incidence of Mycobacterium avium complex (MAC)-induced pulmonary disease (PD) has been increasing in South Korea, posing considerable challenges in treatment. Treatment guidelines recommend initiating therapy after serial computed tomography (CT) monitoring. While drug treatment often improves outcomes in patients with the nodular bronchiectatic (NB) form, those with the fibrocavitary (FC) form may continue to experience persistence despite treatment. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
42 Samples
Download data: XLSX
Series
Accession:
GSE270278
ID:
200270278
5.

The role of interleukin-10 receptor alpha (IL10Rα) in Mycobacterium avium subsp. paratuberculosis infection of a mammary epithelial cell line

(Submitter supplied) Background: Johne’s disease is a chronic wasting disease caused by the bacterium Mycobacterium avium subspecies paratuberculosis (MAP). Johne’s disease is highly contagious and MAP infection in dairy cattle can eventually lead to death. With no available treatment for Johne’s disease, genetic selection and improvements in management practices could help reduce its prevalence. In a previous study, the gene coding interleukin-10 receptor subunit alpha (IL10Rα) was associated with Johne’s disease in dairy cattle. more...
Organism:
Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19172
16 Samples
Download data: CSV
Series
Accession:
GSE247921
ID:
200247921
6.

The Fur-like regulatory protein MAP3773c modulates key metabolic pathways in Mycobacterium avium subsp. paratuberculosis under in-vitro iron starvation

(Submitter supplied) Mycobacterium avium subsp. paratuberculosis (MAP) carries MAP3773c, a putative metal regulator, on its genome which is absent in other mycobacteria. Homologues of this gene in enterobacteria have roles in global iron regulation and homeostasis. The role of MAP3773c in regulating intracellular iron in MAP is poorly understood. Functional analysis of DEGs in ΔMAP3773c revealed that pantothenate (Pan) biosynthesis, polysaccharide biosynthesis, sugar metabolism and N-acetyltransferase enhanced intracellular survival genes were downregulated at 30 minutes post-iron starvation whereas ATP-binding cassette (ABC) type metal transporters, putative siderophore biosynthesis, arginine and proline metabolism, PPE, PE family and mammalian cell entry (MCE) genes were upregulated at that same time point. more...
Organism:
Mycobacterium avium subsp. paratuberculosis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33823
20 Samples
Download data: TXT
Series
Accession:
GSE244734
ID:
200244734
7.

Transcriptome profiling of Pseudomonas syringae pv. syringae 9644 in rich media and hrp-inducing minimum media

(Submitter supplied) Pseudomonas syringae pv. syringae 9644 (Pss9644) is a causal agent of bacterial cherry canker causing necrotic symptoms on leaves, fruits, gummosis and canker in woody tissues of sweet cherry (Prunus avium). To understand which virulent factor genes were expressed in vitro, Pss9644 was grown in rich media (King's B Broth) and minimum media (hrp-inducing minimum media). The latter mimics the in planta environment.
Organism:
Pseudomonas syringae pv. syringae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL34164
6 Samples
Download data: TXT
Series
Accession:
GSE255102
ID:
200255102
8.

Single-cell RNA sequencing analysis according to the clinical course of Mycobacterium avium complex pulmonary disease

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL20795
42 Samples
Download data: CSV, MTX, TSV
Series
Accession:
GSE226473
ID:
200226473
9.

Single-cell TCR sequencing analysis of the course of Mycobacterium avium complex pulmonary disease

(Submitter supplied) We performed scTCR-seq to investigate overall immune cell populations and distribution of MAC-PD patients, according to their clinical outcome.
Organism:
Homo sapiens
Type:
Other
Platform:
GPL20795
21 Samples
Download data: CSV
Series
Accession:
GSE226442
ID:
200226442
10.

Single-cell RNA sequencing analysis of the course of Mycobacterium avium complex pulmonary disease

(Submitter supplied) We performed scRNA-seq to investigate overall immune cell populations and distribution of MAC-PD patients, according to their clinical outcome.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
21 Samples
Download data: MTX, TSV
Series
Accession:
GSE226099
ID:
200226099
11.

Transcriptional profiling of M. intracellulare under acidic and oxidative stress conditions

(Submitter supplied) Mycobacterium avium complex (MAC), including Mycobacterium avium and Mycobacterium intracellulare (MI), accounts for a significant portion of nontuberculous mycobacterial lung disease affecting immunocompromised and lung structural disease patients. Adapting pathogens to a host-induced hostile environment is critical to establishing infection and persistence within the host. However, the cellular and molecular mechanisms of stress response for MAC still need to be elucidated. more...
Organism:
Mycobacterium intracellulare
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33797
9 Samples
Download data: TXT
Series
Accession:
GSE244264
ID:
200244264
12.

Transcriptome analysis of long non-coding RNAs in Mycobacterium avium complex-infected macrophages

(Submitter supplied) Mycobacterium avium complex (MAC) is a non-tuberculosis mycobacteria widely distributed throughout environment. Even though the MAC infection is currently increasing in old women and patients with affected immune system, comprehensive analysis of MAC-infected host cell transcriptome, in particular that of long non-coding RNAs (lncRNAs), has scarcely been reported. Using in vitro cultured primary mouse bone marrow-derived macrophages (BMDMs) and CAGE technology, we analyzed the transcriptional and kinetic landscape of macrophage genes, with focusing on lncRNAs, during MAC infection. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
32 Samples
Download data: TXT
Series
Accession:
GSE249460
ID:
200249460
13.

Dual RNA-sequencing of macrophages infected with Mycobacterium avium reveals host-pathogen interaction in the context of clarithromycin treatment

(Submitter supplied) Background: Mycobacterium avium is an opportunistic pathogen that requires complex multidrug treatment. Macrolides, like clarithromycin, are the cornerstone of treatment, but even macrolide-based treatment regimens have suboptimal outcomes. Combining transcriptomic profiling of macrophages and mycobacteria in an in vitro infection model may increase our understanding of the host-pathogen interaction and the effect of antibiotic treatment. more...
Organism:
Mycobacterium avium subsp. hominissuis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32656
6 Samples
Download data: XLSX
Series
Accession:
GSE213117
ID:
200213117
14.

The potential role of drug transporters and amikacin modifying enzymes in M. avium

(Submitter supplied) Background: Mycobacterium avium complex (MAC) bacteria cause opportunistic infections in humans. Treatment yields cure rates of 60% and is comprised of a macrolide, a rifamycin and ethambutol; and in severe cases amikacin. Mechanisms of antibiotic tolerance remain mostly unknown. To elucidate these mechanisms, we studied the transcriptomic response to antibiotics and investigated the contribution of efflux and amikacin modification to susceptibility. more...
Organism:
Mycobacterium avium subsp. hominissuis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32656
36 Samples
Download data: XLSX
Series
Accession:
GSE213116
ID:
200213116
15.

Trained immunity transplant (TITR) bulk RNA-seq libraries of HSCs

(Submitter supplied) Purpose: To evaluate whether methylation changes occuring upon M. avium infection correlate with transcriptional alterations in trained HSCs, we reisolated CD45.2 untrained vs. trained HSCs (LK CD150+CD48–) from transplanted mice one-month after M. avium challenge to generate bulk RNA-Seq libraries. We compared both libraries to a library from HSCs of WT donor mice following primary M. avium infection. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: CSV
Series
Accession:
GSE197294
ID:
200197294
16.

WT naïve vs. M. avium infected scRNA-seq

(Submitter supplied) purpose: Chronic inflammation induced by Mycobacterium avium infection (timepoint= 1 month) results in transcriptomic changes within the HSC population subset upon bulk RNA-seq, particularly in pathways involved in the immune response, interferon gamma signaling (Th1 immune response) pathway, stat signaling, and antigen processing and presentation. We have also shown that chronic inflammation results in a myeloid differentiation bias of HSPCs. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
2 Samples
Download data: CLOUPE, CSV, H5, MTX, TSV, TXT
Series
Accession:
GSE197407
ID:
200197407
17.

Serum Amyloid A proteins reduce bone mass during mycobacterial infections

(Submitter supplied) To investigate the molecular mechanisms responsible for bone loss during mycobacterial infections
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27583
6 Samples
Download data: TXT
Series
Accession:
GSE215856
ID:
200215856
18.

Transcriptomic analysis of flower bud dormancy in the sweet cherry cultivar 'Fertard'

(Submitter supplied) Temperate perennial plants have to adapt their growth in order to survive over winter conditions and protect their tissues by entering into dormancy. The dormancy phenomenon is a complex process regulated by many factors, externals (photoperiod and temperature) or internals through the transport towards the buds. In order to better understand the molecular mechanisms involved in the regulation of dormancy, we conducted a transcriptomic analysis of flower buds from the late flowering sweet cherry cultivar 'Fertard' during dormancy, from October 2017 to March 2018.
Organism:
Prunus avium
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33329
18 Samples
Download data: TXT
Series
Accession:
GSE229429
ID:
200229429
19.

Cut&Run sequencing of WT HSCs with 1-mon M.avium infection

(Submitter supplied) Purpose: to identify the binding sites for BATF2 in HSCs during M. avium infection, we conducted CUT&RUN sequencing of the HSCs from infected WT mice using an anti-BATF2 antibody. We used an anti-IgG antibody as a control to exclude noise and nonspecific binding and an anti-H3K27ac to assess open chromatin Methods: 10,000-50,000 HSCs (CD45.1/CD45.2 KL CD150+ CD48-) into HBSS from1-month infected WT mice (n=10-12 per group). more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL17021
7 Samples
Download data: XLSX
Series
Accession:
GSE206276
ID:
200206276
20.

Transcriptional and Epigenetic profiling of Batf2 -/- mice in chronic infection

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL17021
23 Samples
Download data: XLSX
Series
Accession:
GSE206277
ID:
200206277
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db=gds|term=Apium%20laetum|query=2|qty=35|blobid=MCID_672f7adbb084802e7536e119|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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