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Items: 1 to 20 of 24

1.

Brain-wide Correspondence Between Neuronal Epigenomics and Long-Distance Projections [5]

(Submitter supplied) Single-cell genetic and epigenetic analyses parse the brain’s billions of neurons into thousands of “cell-type” clusters, each residing in different brain structures. Many of these cell types mediate their unique functions by virtue of targeted long-distance axonal projections to allow interactions between specific cell types. Here we have used Epi-Retro-Seq to link single cell epigenomes and associated cell types to their long-distance projections for 33,034 neurons dissected from 32 different source regions projecting to 24 different targets (225 source→target combinations) across the whole mouse brain. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL24247
7868 Samples
Download data: TSV
Series
Accession:
GSE231442
ID:
200231442
2.

Brain-wide Correspondence Between Neuronal Epigenomics and Long-Distance Projections [4]

(Submitter supplied) Single-cell genetic and epigenetic analyses parse the brain’s billions of neurons into thousands of “cell-type” clusters, each residing in different brain structures. Many of these cell types mediate their unique functions by virtue of targeted long-distance axonal projections to allow interactions between specific cell types. Here we have used Epi-Retro-Seq to link single cell epigenomes and associated cell types to their long-distance projections for 33,034 neurons dissected from 32 different source regions projecting to 24 different targets (225 source→target combinations) across the whole mouse brain. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL24247
8000 Samples
Download data: TSV
Series
Accession:
GSE231414
ID:
200231414
3.

Brain-wide Correspondence Between Neuronal Epigenomics and Long-Distance Projections [3]

(Submitter supplied) Single-cell genetic and epigenetic analyses parse the brain’s billions of neurons into thousands of “cell-type” clusters, each residing in different brain structures. Many of these cell types mediate their unique functions by virtue of targeted long-distance axonal projections to allow interactions between specific cell types. Here we have used Epi-Retro-Seq to link single cell epigenomes and associated cell types to their long-distance projections for 33,034 neurons dissected from 32 different source regions projecting to 24 different targets (225 source→target combinations) across the whole mouse brain. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL24247
8000 Samples
Download data: TSV
Series
Accession:
GSE231326
ID:
200231326
4.

Taxonomy of fibroblasts and progenitors in the synovial joint at single-cell resolution

(Submitter supplied) Objectives. Fibroblasts in synovium include fibroblast-like synoviocytes (FLS) in the lining and Thy1+ connective-tissue fibroblasts in the sub-lining. We aimed to investigate their developmental origin and relationship with adult progenitors. Methods. To discriminate between Gdf5-lineage cells deriving from the embryonic joint interzone and other Pdgfrα-expressing fibroblasts and progenitors, adult Gdf5-Cre;Tom;Pdgfrα-H2BGFP mice were used and cartilage injury was induced to activate progenitors. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
9 Samples
Download data: MTX, TSV
Series
Accession:
GSE214500
ID:
200214500
5.

Transcriptomic characterization of a mixed population of pluripotent stem cell derived cerebellar neuron-like progenitors

(Submitter supplied) We set out to ascertain whether it was possible to use PSCs (pluripotent stem cells) to generate a mix of neuronal cell types resembling those in the cerebellum, most notably Purkinje and granule cells. Several groups have previously demonstrated generation of cerebellar-like neuronal cells from murine ESCs (embryonic stem cells), and more recently the Erceg group achieved similar success using human PSCs. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: TXT
Series
Accession:
GSE65423
ID:
200065423
6.

Global transcriptomic changes of either cell cycle arrested parasites or cell cycle re-entered asexual P. falciparum 3D7 parasites.

(Submitter supplied) Parasitic protists, including Plasmodium falciparum malaria parasites, evolved sophisticated biological features to adapt and survive in e.g. mosquito vectors and mammalian hosts. The parasite’s life cycle is extraordinarily controlled, oscillating between quiescent stages (e.g. sporozoites or gametocytes) and stages of intense proliferation. The atypical mode of asexual reproduction in erythrocytes (schizogony: asynchronous nuclear division in the absence of cytokinesis), is clearly divergent from cell division in higher eukaryotes but the mechanisms that control cell cycle progression are poorly understood. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL17233
32 Samples
Download data: GPR
Series
Accession:
GSE92289
ID:
200092289
7.

Molecular signatures of neural connectivity in the olfactory cortex

(Submitter supplied) Purpose:This work aimed to identify the genetic profiles of piriform projection neurons and characterize their spatial organization within the piriform cortex. Methods: We microdissected the three layers of pirifrom cortex by laser capture (LMD) and performed RNA deep sequencing in order to identify layer-specific molecular markers, we then validated these data by using RNA in situ hybridization and immunohistochemistry.We next performed anterograde neural tracing experiments to identify piriform target regions, and retrograde neural tracing experiments to analyze how piriform projection neurons are organized within piriform cortex.We then combined the analysis of patterns of gene expression with retrograde tracing experiments to identify molecular signatures of the different subclasses of piriform projecting neurons. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18480
9 Samples
Download data: TSV
Series
Accession:
GSE70800
ID:
200070800
8.

Wide-scale transcriptome disturbance underlies liver and kidney pathology from chronic ultra low dose Roundup exposure [kidney]

(Submitter supplied) Glyphosate-based herbicides (GBH) are the major pesticides used worldwide. Converging evidence suggests that GBH residues pose a particular risk to the kidneys and liver. However, the existence of biological effects with negative health implications at low environmentally relevant doses remains unresolved. A previous investigation addressed this issue, by conducting a 2-year feeding study, which included 10 female Sprague Dawley rats administered via drinking water with 0.1 ppb of a major Roundup formulation (50 ng/L glyphosate equivalent dilution). more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
19 Samples
Download data: CEL
Series
Accession:
GSE66059
ID:
200066059
9.

Wide-scale transcriptome disturbance underlies liver and kidney pathology from chronic ultra low dose Roundup exposure [liver]

(Submitter supplied) Glyphosate-based herbicides (GBH) are the major pesticides used worldwide. Converging evidence suggests that GBH residues pose a particular risk to the kidneys and liver. However, the existence of biological effects with negative health implications at low environmentally relevant doses remains unresolved. A previous investigation addressed this issue, by conducting a 2-year feeding study, which included 10 female Sprague Dawley rats administered via drinking water with 0.1 ppb of a major Roundup formulation (50 ng/L glyphosate equivalent dilution). more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
20 Samples
Download data: CEL
Series
Accession:
GSE66058
ID:
200066058
10.

UV-B dose and time range finding study on mouse biopsy skin samples

(Submitter supplied) In molecular biology, the design of mechanistic experiments has to be optimized by considering statistical and biological principles. In contrast to statistical principles, biological principles of experimental design are not universally formulated. In an attempt to pinpoint generally acceptable rules, we investigated the importance of determining the optimal ranges of scale of i.e. dose and time in gene expression experiments. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17736
57 Samples
Download data: FTR
Series
Accession:
GSE51348
ID:
200051348
11.

UV-C dose and time range finding study on Mouse Embryonic Fibroblasts (MEFs)

(Submitter supplied) In molecular biology, the design of mechanistic experiments has to be optimized by considering statistical and biological principles. In contrast to statistical principles, biological principles of experimental design are not universally formulated. In an attempt to pinpoint generally acceptable rules, we investigated the importance of determining the optimal ranges of scale of i.e. dose and time in gene expression experiments. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17736
48 Samples
Download data: FTR
Series
Accession:
GSE50930
ID:
200050930
12.

Expression data from Foxl2 wild-type and mutant ovaries and testes

(Submitter supplied) Foxl2 is a forkhead transcription factor expressed only in the female, but not in the male gonad. We have created mice homozygous mutant for the Foxl2 gene (KO) as well as mice carrying a conditional mutant Foxl2 allele (floxed). The expression profiles of conventional Foxl2 knockout and wildtype ovaries were compared at P3, using the Affy Mouse Genome 430 2.0 Array. Adult wildtype and conditional mutant (Foxl2 floxed x RosaCre-EBD treated with tamoxifen) ovaries were compared to adult wildtype testes using the Affymetrix Mouse Gene 1.0 ST Array. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL1261 GPL6246
12 Samples
Download data: CEL
Series
Accession:
GSE16853
ID:
200016853
13.

Ovary at P3, Foxl2 KO, replicate 2

Organism:
Mus musculus
Source name:
Mouse ovary, P3, Foxl2 KO
Platform:
GPL1261
Series:
GSE16853
Download data: CEL
Sample
Accession:
GSM422402
ID:
300422402
14.

Ovary at P3, Foxl2 KO, replicate 1

Organism:
Mus musculus
Source name:
Mouse ovary, P3, Foxl2 KO
Platform:
GPL1261
Series:
GSE16853
Download data: CEL
Sample
Accession:
GSM422401
ID:
300422401
15.

Ovary at P3, wild-type, replicate 2

Organism:
Mus musculus
Source name:
Mouse ovary, P3, wildtype
Platform:
GPL1261
Series:
GSE16853
Download data: CEL
Sample
Accession:
GSM422400
ID:
300422400
16.

Ovary at P3, wild-type, replicate 1

Organism:
Mus musculus
Source name:
Mouse ovary, P3, wildtype
Platform:
GPL1261
Series:
GSE16853
Download data: CEL
Sample
Accession:
GSM422399
ID:
300422399
17.

Adult ovary, Foxl2 mutant, replicate 3

Organism:
Mus musculus
Source name:
Mouse ovary, adult,Foxl2 flox/flox x CreEBD
Platform:
GPL6246
Series:
GSE16853
Download data: CEL
Sample
Accession:
GSM422398
ID:
300422398
18.

Adult ovary, Foxl2 mutant, replicate 2

Organism:
Mus musculus
Source name:
Mouse ovary, adult,Foxl2 flox/flox x CreEBD
Platform:
GPL6246
Series:
GSE16853
Download data: CEL
Sample
Accession:
GSM422397
ID:
300422397
19.

Adult ovary, Foxl2 mutant, replicate 1

Organism:
Mus musculus
Source name:
Mouse ovary, adult,Foxl2 flox/flox x CreEBD
Platform:
GPL6246
Series:
GSE16853
Download data: CEL
Sample
Accession:
GSM422396
ID:
300422396
20.

Adult ovary, wild-type, replicate 2

Organism:
Mus musculus
Source name:
Mouse ovary, adult, wildtype
Platform:
GPL6246
Series:
GSE16853
Download data: CEL
Sample
Accession:
GSM422395
ID:
300422395
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