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Links from GEO DataSets

Items: 5

1.

Expression profiling of FRG1 transgenic mice.

(Submitter supplied) RNA from skeletal muscle of mice over-expressing selectively in the skeletal muscle the gene FRG1, a candidate of facioscapulohumeral muscular dystrophy, was compared to RNA from skeletal muscle of WT mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6105
6 Samples
Download data: TXT
Series
Accession:
GSE28575
ID:
200028575
2.

Rbfox1 downregulation and altered Calpain 3 splicing by FRG1 in a mouse model of facioscapulohumeral muscular dystrophy (FSHD).

(Submitter supplied) FRG1 over-expression results in an FSHD-like phenotype in mice. Muscles (vastus lateralis and biceps brachii) from wild type and FRG1 over-expressing mice were compared at 4 and 13 weeks of age by splicing sensitive microarray.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13185
24 Samples
Download data: CEL
Series
Accession:
GSE32073
ID:
200032073
3.

Effect of facioscapulohumeral dystrophy (FSHD) on skeletal muscle gene expression

(Submitter supplied) Muscle biopsies taken from vastus lateralis muscle of 30 normal subjects and 19 FSHD subjects (see PubMed ID 17151338) Affymetrix U133A and U133B arrays were scanned both before (S1) and after (S2) antibody enhancement. Effects of age and sex in normal subjects reported previously under GSE362, GSE674, and GSE9676. Keywords: facioscapulohumeral dystrophy, skeletal muscle
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL96 GPL97
196 Samples
Download data: CEL
Series
Accession:
GSE10760
ID:
200010760
4.

Expression profiling FSHD vs. control myoblasts and myotubes

(Submitter supplied) The gene expression pathways leading to muscle pathology in facioscapulohumeral dystrophy (FSHD) remain to be elucidated. This muscular dystrophy is caused by a contraction of an array of tandem 3.3-kb repeats (D4Z4) at 4q35.2. We compared expression of control and FSHD myoblasts and myotubes (three preparations each) on exon microarrays (Affymetrix Human Exon 1.0 ST) and validated FSHD-specific differences for representative genes by qRT-PCR on additional myoblast cell strains. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE26145
ID:
200026145
5.

P38α Regulates Expression of DUX4 in Facioscapulohumeral Muscular Dystrophy

(Submitter supplied) Here, we describe the identification and characterization of p38α as a novel regulator of DUX4 expression in FSHD myotubes. By using multiple highly characterized, potent and specific inhibitors of p38α/β, we show a robust reduction of DUX4 expression, activity and cell death across FSHD1 and FSHD2 patient-derived lines. RNA-seq profiling reveals that a small number of genes are differentially expressed upon p38α/β inhibition, the vast majority of which are DUX4 target genes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
12 Samples
Download data: XLSX
Series
Accession:
GSE153301
ID:
200153301
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