Expression data from thalamus or parietal lobe of FFI patients and normal human.
Source: NCBI BioProject (ID PRJNA174309)
Source: NCBI BioProject (ID PRJNA174309)
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Project name: Homo sapiens
Description: Fatal familial insomnia (FFI) is a special subtype of genetic human prion diseases that is caused by the D178N mutation of the prion protein gene (PRNP). In this study, global expression patterns of the thalamus and parietal cortex from three patients with FFI were analyzed by Affymetrix Human Genome U133+ 2.0 chip.We used microarrays to detail the global gene expression in tissues from normal human and FFI patients thalamus, or parietal lobe.Overall design: Tissues from normal human and FFI patients' thalamus, or parietal lobe were for RNA extraction and hybridization on Affymetrix microarrays.
Data type: Transcriptome or Gene expression
Sample scope: Multiisolate
Relevance: Medical
Organization: Chinese Center for Disease Control and Prevention, China CDC
Literatures
- PMID: 24902808
Last updated: 2012-09-04