Sign in to NCBI

Display Settings:

Format

Send to:

Choose Destination
Accession: PRJNA175137 ID: 175137

Homo sapiens (human)

Global gene expression analysis for neuron stem cells (NSC) derived from iPSCs with Fanconi Anemia

See Genome Information for Homo sapiens
Navigate Across
66644 additional projects are related by organism.
Fanconi Anemia (FA) is a recessive disorder associated with genomic instability We generated iPSC from FA patient fibroblasts and further corrected the mutated FANCA gene with a homologous recombination-based approach. More...
AccessionPRJNA175137; GEO: GSE40865
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
PublicationsLiu GH et al., "Modelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCs.", Nat Commun, 2014 Jul 7;5:4330
SubmissionRegistration date: 13-Sep-2012
GEL-B, Salk Institute
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots444555
Data volume, Processed Mbytes11
Data volume, Supplementary Mbytes20

Supplemental Content

Related information

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI
Support Center