Homo sapiens (ID 232852) - BioProject

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Accession: PRJNA232852 ID: 232852

Homo sapiens (human)

An Epigenetic Signature in Peripheral Blood Associated with Neurodegenerative Tauopathy and the Risk-Associated Haplotype on 17q21.31

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90127 additional projects are related by organism.

Progressive supranuclear palsy (PSP) and frontotemporal dementia (FTD) are two neurodegenerative diseases linked, at the pathologic and genetic level, to the macrutubule associated protein tau. More...

Accession	PRJNA232852; GEO: GSE53740
Data Type	Epigenomics
Scope	Multiisolate
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Publications	Cho SH et al., "SIRT1 deficiency in microglia contributes to cognitive decline in aging and neurodegeneration via epigenetic regulation of IL-1β.", J Neurosci, 2015 Jan 14;35(2):807-18 Li Y et al., "An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy.", PLoS Genet, 2014 Mar;10(3):e1004211
Submission	Registration date: 31-Dec-2013 Neurogenetics, Psychiatry and Neurology, UCLA
Relevance	Medical

Project Data:

Resource Name	Number of Links
Publications
PubMed	2
PMC	2
Other datasets
GEO DataSets	1

GEO Data Details

Parameter	Value
Data volume, Spots	186461568
Data volume, Processed Mbytes	5664
Data volume, Supplementary Mbytes	934

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Homo sapiens (human)

An Epigenetic Signature in Peripheral Blood Associated with Neurodegenerative Tauopathy and the Risk-Associated Haplotype on 17q21.31

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