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Accession: PRJNA227344 ID: 227344

Homo sapiens (human)

A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging

See Genome Information for Homo sapiens
Our data throw light upon the effect of WRN deficiency on gene expression and epigenomic modification, which indicates aging-associated changes from both genomic and epigenomic level. More...
AccessionPRJNA227344; GEO: GSE52285
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsZhang W et al., "Aging stem cells. A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging.", Science, 2015 Jun 5;348(6239):1160-3
SubmissionRegistration date: 12-Nov-2013
Peking University
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments22
Publications
PubMed1
PMC1
Other datasets
BioSample22
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes856
SRA Data Details
ParameterValue
Data volume, Gbases38
Data volume, Mbytes24674

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  • Homo sapiens
    Homo sapiens
    A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging
    BioProject
  • SRX376714 (1)
    SRA

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