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Accession: PRJNA172869 ID: 172869

Homo sapiens (human)

Deregulation of miRNAs in Infant Outflow Tract Myocardium of Non-syndromic Tetralogy of Fallot

See Genome Information for Homo sapiens
Tetralogy of Fallot (TOF) is one of the most common heart defects in children and the underlying mechanisms remain elusive. More...
AccessionPRJNA172869; GEO: GSE40128
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
SubmissionRegistration date: 15-Aug-2012
Fudan University
RelevanceMedical
Project Data:
Resource NameNumber
of Links
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots62304
Data volume, Processed Mbytes2
Data volume, Supplementary Mbytes2

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