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Accession: PRJNA174576 ID: 174576

Homo sapiens (human)

Transcriptional analysis of whole blood in patients with auto-inflammatory disorders

See Genome Information for Homo sapiens
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This project is a component of the Transcriptional analysis of whole blood, primary fibroblasts, and PBMCs upon TNF-alpha or IL-1beta stimulation from HOIL-1-deficient patients
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2 additional projects are components of the Transcriptional analysis of whole blood, primary fibroblasts, and PBMCs upon TNF-alpha or IL-1beta stimulation from HOIL-1-deficient patients.
66644 additional projects are related by organism.
HOIL1 deficient disease is a new early onset fatal autosomal recessive human disorder charaterized by chronic auto-inflammation, recurrent invasive bacterial infections and progressive muscular amylopectinosis. More...
AccessionPRJNA174576; GEO: GSE40561
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
PublicationsBoisson B et al., "Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency.", Nat Immunol, 2012 Dec;13(12):1178-86
SubmissionRegistration date: 3-Sep-2012
Virginia Pascual, Baylor Institute for Immunology Research, Baylor Research Institute
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots2488953
Data volume, Processed Mbytes74
Data volume, Supplementary Mbytes16

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