Homo sapiens (ID 159231) - BioProject

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Accession: PRJNA159231 ID: 159231

Homo sapiens (human)

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Klinefelter’s Syndrome (KS) is one of the common chromosome aneuploidy diseases in males with unexplained physiological mechanism. More...

Accession	PRJNA159231; GEO: GSE37258
Data Type	Transcriptome or Gene expression
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	Ma Y et al., "Aberrant gene expression profiles in pluripotent stem cells induced from fibroblasts of a Klinefelter syndrome patient.", J Biol Chem, 2012 Nov 9;287(46):38970-9
Submission	Registration date: 13-Apr-2012 Institute of Health Sciences
Relevance	Medical

Project Data:

Parameter	Value
Data volume, Spots	984150
Data volume, Processed Mbytes	20
Data volume, Supplementary Mbytes	74

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