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Series GSE36398 Query DataSets for GSE36398
Status Public on Sep 19, 2012
Title Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Facioscapulohumeral muscular dystrophy (FSHD) is a progressive neuromuscular disorder caused by contractions of repetitive elements within the macrosatellite D4Z4 on chromosome 4q35. In order to develop mRNA-based biomarkers of affected muscles, we used GeneChip Gene 1.0 ST arrays for global analysis of gene expression in muscle biopsy specimens obtained from FSHD subjects and their unaffected first degree relatives.
 
Overall design FSHD typically affects biceps muscles more severely than deltoid muscles. To examine muscle-specific expression changes associated with FSHD while controlling for background genetic variation, we analyzed RNA extracted from both biceps and deltoids of FSHD subjects and unaffected first-degree relatives.
 
Contributor(s) Rahimov F
Citation(s) 22988124
Submission date Mar 09, 2012
Last update date Jul 26, 2018
Contact name Fedik Rahimov
E-mail(s) [email protected]
Phone 617-355-4042
Fax 617-730-0253
Organization name Boston Children's Hospital
Department Genetics
Lab Kunkel
Street address 3 Blackfan Circle, CLS 15030.4
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platforms (1)
GPL6244 [HuGene-1_0-st] Affymetrix Human Gene 1.0 ST Array [transcript (gene) version]
Samples (50)
GSM892341 Deltoid, FSHD, cohort 03, subject 03A
GSM892342 Biceps, FSHD, cohort 03, subject 03A
GSM892343 Deltoid, control, cohort 03, subject 03U
Relations
BioProject PRJNA153289

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
GSE36398_RAW.tar 205.3 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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