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Series GSE43698 Query DataSets for GSE43698
Status Public on Jan 20, 2015
Title Muscle from patients with mitochondrial myopathies and congenital muscular dystrophies versus normal human muscle
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Global gene expression analysis was performed comparing human skeletal muscle samples from patients with various forms of muscular dystrophy and mitochondrial myopathies in order to identify specific gene expression changes associated with collagen VI deficiency (leading to Ullrich┬┤s Congenital Muscular Dystrophy) and depletion of mitochondrial DNA relative to other mitochondrial myopathies
 
Overall design We analysed the gene expression profile of skeletal muscle from children suffering from mitochondrial myopathies and various forms of muscular dystrophy relative to skeletal muscle from healthy children using commercially available arrays that represents the complete human genome (Agilent Human SurePrintGE, 8x60K )
 
Contributor(s) Kalko S, Jimenez-Mallebrera C, Paco S
Citation(s) 24484525
Submission date Jan 23, 2013
Last update date Nov 27, 2018
Contact name Susana Kalko
E-mail(s) kalko.susana@gmail.com
Organization name IDIBAPS
Department Bioinformatics Platform
Street address c/Rosello 153
City Barcelona
State/province BARCELONA
ZIP/Postal code 08036
Country Spain
 
Platforms (1)
GPL13607 Agilent-028004 SurePrint G3 Human GE 8x60K Microarray (Feature Number version)
Samples (29)
GSM1068568 Control-1
GSM1068569 Control-2
GSM1068570 Control-3
Relations
BioProject PRJNA187082

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE43698_RAW.tar 358.9 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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