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Accession: PRJNA285353 ID: 285353

Homo sapiens (human)

Expression data from young and old healthy humans, as well as HGPS patients

See Genome Information for Homo sapiens
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66643 additional projects are related by organism.
HGPS is a rare premature ageing disease, caused by a mutation in the LMNA gene, which activates a cryptic splice site, resulting in the production of a mutant lamin A isoform, called progerin. More...
AccessionPRJNA285353; GEO: GSE69391
Data TypeTranscriptome or Gene expression
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsKubben N et al., "Repression of the Antioxidant NRF2 Pathway in Premature Aging.", Cell, 2016 Jun 2;165(6):1361-1374
SubmissionRegistration date: 29-May-2015
NCI, NIH
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots656100
Data volume, Processed Mbytes14
Data volume, Supplementary Mbytes63

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