U.S. flag

An official website of the United States government

Display Settings:

Format

Send to:

Choose Destination
Accession: PRJNA219382 ID: 219382

Homo sapiens (human)

Genomic localization of Cockayne syndrom B protein upon genotoxic stresses

See Genome Information for Homo sapiens
Cockayne syndrome is an inherited premature aging syndrome associated with developmental and neurological disorders. More...
AccessionPRJNA219382; GEO: GSE50925
Data TypeEpigenomics
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsLake RJ et al., "The CSB chromatin remodeler and CTCF architectural protein cooperate in response to oxidative stress.", Nucleic Acids Res, 2016 Mar 18;44(5):2125-35
SubmissionRegistration date: 17-Sep-2013
The University of Pennsylvania
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments2
Publications
PubMed1
PMC1
Other datasets
BioSample2
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes1
SRA Data Details
ParameterValue
Data volume, Gbases5
Data volume, Mbytes3818

Supplemental Content

Recent activity

  • Homo sapiens
    Homo sapiens
    Genomic localization of Cockayne syndrom B protein upon genotoxic stresses
    BioProject

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center