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accession-icon GSE20186
Systematic meta-analysis and replication of genome-wide expression studies of Parkinson's disease
  • organism-icon Homo sapiens
  • sample-icon 36 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133A Array (hgu133a), Illumina HumanHT-12 V3.0 expression beadchip

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.

Sample Metadata Fields

Sex, Age, Specimen part, Disease

View Samples
accession-icon GSE20146
Expression analysis of dissected GPi in Parkinson's disease
  • organism-icon Homo sapiens
  • sample-icon 20 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

Genome-wide transcriptome analysis of expression changes in Globus Pallidus interna (GPi) from Parkinson's disease brain tissue versus control brain tissue.

Publication Title

PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.

Sample Metadata Fields

Sex, Specimen part, Disease, Disease stage

View Samples
accession-icon GSE20141
Expression analysis of laser-dissected SNpc neurons in Parkinson's disease
  • organism-icon Homo sapiens
  • sample-icon 16 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

Genome-wide transcriptome analysis of expression changes in laser-dissected SNpc neurons from Parkinson's disease brain tissue versus control brain tissue.

Publication Title

PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.

Sample Metadata Fields

Specimen part, Disease, Disease stage

View Samples
accession-icon GSE20163
Systematic meta-analysis and replication of genome-wide expression studies of Parkinson's disease: 2
  • organism-icon Homo sapiens
  • sample-icon 17 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133A Array (hgu133a)

Description

Systematic meta-analysis and replication of genome-wide expression studies identifies molecular pathways of Parkinson's disease.

Publication Title

PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.

Sample Metadata Fields

Age, Specimen part, Disease

View Samples
accession-icon GSE20153
Expression analysis of lymphoblast cells lines in Parkinson's disease
  • organism-icon Homo sapiens
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

Genome-wide transcriptome analysis of expression changes in EBV transformed cell lines from the Coriell Cell Repository in Parkinson and Control subjects.

Publication Title

PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.

Sample Metadata Fields

Sex, Disease, Disease stage

View Samples
accession-icon GSE20164
Systematic meta-analysis and replication of genome-wide expression studies of Parkinson's disease: 3
  • organism-icon Homo sapiens
  • sample-icon 11 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133A Array (hgu133a)

Description

Systematic meta-analysis and replication of genome-wide expression studies identifies molecular pathways of Parkinson's disease.

Publication Title

PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.

Sample Metadata Fields

Sex, Age, Specimen part, Disease

View Samples
accession-icon GSE20314
Systematic meta-analysis and replication of genome-wide expression studies of Parkinsons disease: 4
  • organism-icon Homo sapiens
  • sample-icon 8 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133A Array (hgu133a)

Description

Analysis of substantia nigra from postmortem brains of 4 patients with Parkinsons disease (PD). Results provide insight into the molecular processes perturbed in the PD substantia nigra.

Publication Title

PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.

Sample Metadata Fields

Sex, Age, Specimen part, Disease

View Samples
accession-icon GSE28037
Gene expression data from WT and SREBP-1a deficient macrophages
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.0 ST Array (mogene10st)

Description

Gene expression from bone-marrow drived macrophages of WT and SREBP-1a deficient mice

Publication Title

Linking lipid metabolism to the innate immune response in macrophages through sterol regulatory element binding protein-1a.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE103622
Gene expression data from irradiated mouse liver
  • organism-icon Mus musculus
  • sample-icon 2 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 2.0 ST Array (mogene20st)

Description

In previous studies, it was observed that survivors who received stem cell transplantation and whole body irradiation showed development of NAFLD as a chronic effect.

Publication Title

Decreased Hepatic Lactotransferrin Induces Hepatic Steatosis in Chronic Non-Alcoholic Fatty Liver Disease Model.

Sample Metadata Fields

Sex, Age, Specimen part

View Samples
accession-icon GSE64264
Functional Retinal Pigment Epithelium-like Cells from Human Fibroblasts
  • organism-icon Homo sapiens
  • sample-icon 2 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

The retinal pigment epithelium (RPE) provides vital support to photoreceptor cells and its dysfunction is associated with the onset and progression of age-related macular degeneration (AMD). Surgical provision of RPE cells may ameliorate AMD and thus it would be valuable to develop sources of patient-matched RPE cells for this application of regenerative medicine. We describe here the generation of functional RPE-like cells from fibroblasts that represent an important step toward that goal. We identified candidate master transcriptional regulators of RPEs using a novel computational method and then used these regulators to guide exploration of the transcriptional regulatory circuitry of RPE cells and to reprogram human fibroblasts into RPE-like cells. The RPE-like cells share key features with RPEs derived from healthy individuals, including morphology, gene expression and function, and thus represent a step toward the goal of generating patient-matched RPE cells for treatment of macular degeneration.

Publication Title

A Systematic Approach to Identify Candidate Transcription Factors that Control Cell Identity.

Sample Metadata Fields

Specimen part

View Samples
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refine.bio is a repository of uniformly processed and normalized, ready-to-use transcriptome data from publicly available sources. refine.bio is a project of the Childhood Cancer Data Lab (CCDL)

fund-icon Fund the CCDL

Developed by the Childhood Cancer Data Lab

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Cite refine.bio

Casey S. Greene, Dongbo Hu, Richard W. W. Jones, Stephanie Liu, David S. Mejia, Rob Patro, Stephen R. Piccolo, Ariel Rodriguez Romero, Hirak Sarkar, Candace L. Savonen, Jaclyn N. Taroni, William E. Vauclain, Deepashree Venkatesh Prasad, Kurt G. Wheeler. refine.bio: a resource of uniformly processed publicly available gene expression datasets.
URL: https://www.refine.bio

Note that the contributor list is in alphabetical order as we prepare a manuscript for submission.

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