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Links from GEO DataSets

Items: 20

1.
Full record GDS638

Dystrophin-deficient mdx diaphram muscle development time course

Temporal analysis of diaphram muscle from dystrophin-deficient mdx mice, a Duchenne muscular dystrophy (DMD) model. Postnatal ages 7 to 112 days examined. Results provide insight into mechanisms of muscular dystrophy pathogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 6 age, 2 strain sets
Platform:
GPL81
Series:
GSE1026
36 Samples
Download data: CEL
DataSet
Accession:
GDS638
ID:
638
2.

Diaphram, comparison of wild type and mdx mice, 7 to 112 Days (Porter lab)

(Submitter supplied) Determination of gene expression changes in extraocular muscle of mdx (dystrophin-deficient) mice at postnatal ages 7, 14, 23, 28, 56, and 112 days. 3 independent replicates/age/strain. Data form part of publication: Human Molecular Genetics 13:257-269, 2004. Keywords = microarray Keywords = muscle Keywords: time-course
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS638
Platform:
GPL81
36 Samples
Download data: CEL
Series
Accession:
GSE1026
ID:
200001026
3.

Laminin-deficient muscular dystrophy, dy/dy diaphragm

(Submitter supplied) Laminin (merosin) deficient muscular dystrophy in dy/dy mouse diaphragm muscle, 8 weeks old Keywords: muscle, muscular dystrophy, laminin, merosin, diaphragm, mouse
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1778
Platform:
GPL339
8 Samples
Download data
Series
Accession:
GSE3252
ID:
200003252
4.
Full record GDS1778

Alpha2-laminin deficient dy/dy model of muscular dystrophy: diaphragm

Analysis of diaphragms of alpha2-laminin deficient dy/dy animals. Alpha-2 laminin is important in muscle cell attachment, and its deficiency underlies classical congenital muscular dystrophy. Results provide insight into the events that link alpha2-laminin deficiency with muscle fiber necrosis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL339
Series:
GSE3252
8 Samples
Download data
DataSet
Accession:
GDS1778
ID:
1778
5.

Extraocular muscle, comparison of wild type and mdx mice, 14 to 112 Days (Porter lab)

(Submitter supplied) Determination of gene expression changes in extraocular muscle of mdx (dystrophin-deficient) mice at postnatal ages 14, 28, 56, and 112 days. 3 independent replicates/age/strain. Keywords = microarray Keywords = muscle Keywords: time-course
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS614
Platform:
GPL81
24 Samples
Download data: CEL
Series
Accession:
GSE1008
ID:
200001008
6.
Full record GDS614

Dystrophin-deficient mdx extraocular muscle development time course

Analysis of extraocular muscle (EOM) from dystrophin-deficient mdx mice, a Duchenne muscular dystrophy (DMD) model. Postnatal ages 14, 28, 56, and 112 days examined. EOM is unaffected in DMD, so results provide insight into mdx EOM protective mechanisms.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 age, 2 strain sets
Platform:
GPL81
Series:
GSE1008
24 Samples
Download data: CEL
DataSet
Accession:
GDS614
ID:
614
7.

Hindlimb muscle, comparison of wild type and mdx mice, 7 to 112 Day (Porter lab)

(Submitter supplied) Determination of gene expression changes in hindlimb muscle (gastrocnemius/soleus) of mdx (dystrophin-deficient) mice at postnatal ages 7, 14, 23, 28, 56, and 112. Keywords: time-course
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS639
Platform:
GPL81
36 Samples
Download data: CEL
Series
Accession:
GSE1025
ID:
200001025
8.
Full record GDS639

Dystrophin-deficient mdx hindlimb muscle development time course

Temporal analysis of hindlimb gastrocnemius/soleus muscle from dystrophin-deficient mdx mice, a Duchenne muscular dystrophy (DMD) model. Postnatal ages 7 to 112 days examined. Results provide insight into mechanisms of muscular dystrophy pathogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 6 age, 2 strain sets
Platform:
GPL81
Series:
GSE1025
36 Samples
Download data: CEL
DataSet
Accession:
GDS639
ID:
639
9.

Mouse Models for Muscular Dystrophy

(Submitter supplied) Comparative analysis of gene expression levels from hindlimb muscle tissue from 8 week old mouse models for muscular dystrophy. We have used mouse models with dystrophin-, sarcoglycan-, sarcospan-, or dysferlin-deficiency. Keywords = muscular dystrophy Keywords: other
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1770
26 Samples
Download data
Series
Accession:
GSE2112
ID:
200002112
10.

Molecular profiles of dystrophin-deficient and normal murine muscle

(Submitter supplied) Expression profiles of six skeletal muscle types in mdx, mdx5cv and wildtype mice. Keywords: other
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS641
Platform:
GPL81
36 Samples
Download data: CEL, EXP, RPT
Series
Accession:
GSE897
ID:
200000897
11.
Full record GDS641

Dystrophin-deficient mdx, mdx5cv and wild type skeletal muscle profiles

Analysis of diaphragm, extensor digitorum longus, gastroc, soleus, quadricep, and tibialis anterior muscle in 8 week old male dystrophin-deficient mdx, mdx5cv, and C57BL10 wild type provides insight into pathogenesis of muscular dystrophy.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 strain, 6 tissue sets
Platform:
GPL81
Series:
GSE897
36 Samples
Download data: CEL, EXP, RPT
DataSet
Accession:
GDS641
ID:
641
12.

Extraocular and hindlimb muscle, comparison of wild type and mdx mice, 56 days (Porter lab)

(Submitter supplied) Determination of gene expression changes in extraocular and hindlimb (gastrocnemius/soleus) of mdx (dystrophin-deficient) mice at postnatal day 56. 5 independent replicates/muscle group/strain. Keywords: parallel sample
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS703
Platform:
GPL32
20 Samples
Download data: CEL
Series
Accession:
GSE1472
ID:
200001472
13.
Full record GDS703

Dystrophin-deficient mdx extraocular and leg muscle

Analysis of extraocular (EOM) and hindlimb (gastrocnemius/soleus) muscle in mdx (dystrophin-deficient; Duchenne muscular dystrophy model) mice at postnatal day 56.5. Highly specific changes observed between dystrophic (leg) and spared (EOM) muscle.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 strain, 2 tissue sets
Platform:
GPL32
Series:
GSE1472
20 Samples
Download data: CEL
DataSet
Accession:
GDS703
ID:
703
14.

mRNA expression in regenerated mdx mouse skeletal muscle

(Submitter supplied) Despite over 3,000 articles published on dystrophin in the last 15 years, the reasons underlying the progression of the human disease, differential muscle involvement, and disparate phenotypes in different species are not understood. The present experiment employed a screen of 12,488 mRNAs in 16-wk-old mouse mdx muscle at a time when the skeletal muscle is avoiding severe dystrophic pathophysiology, despite the absence of a functional dystrophin protein. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS236
Platform:
GPL81
10 Samples
Download data: CEL
Series
Accession:
GSE466
ID:
200000466
15.
Full record GDS236

Dystrophin-deficient mdx muscle regeneration

Examination of mdx mouse, Duchenne muscular dystrophy model. 16 week regenerating mdx muscle analyzed in search for salvage pathways that maintain skeletal muscle integrity in the absence of functional dystrophin protein.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 strain sets
Platform:
GPL81
Series:
GSE466
10 Samples
Download data: CEL
DataSet
Accession:
GDS236
ID:
236
16.

A transcriptional map of the impact of endurance exercise training on skeletal muscle phenotype

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL9454 GPL570
65 Samples
Download data: CEL
Series
Accession:
GSE35661
ID:
200035661
17.

Time-course of mdx and wild type mice

(Submitter supplied) Time-course microarray data set of mdx and wild type mice ranging from 1-20 weeks of age Keywords: time-course
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL485
36 Samples
Download data
Series
Accession:
GSE1574
ID:
200001574
18.

Expression data from quadriceps muscle of young DMD patients and age matched controls

(Submitter supplied) Albeit increased serum CK level and abnormal muscle histology are always present, boys with DMD are phenotipically indistinguishable from the normal ones at birth and, in their first years of life, acquire early motor milestones at normal times. A clear defect in muscle function becomes generally apparent by the end of the second year. As the disease is typically diagnosed between the ages of 3 and 7, the first two years are often considered and referred to as clinically presymptomatic. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3027
Platform:
GPL96
37 Samples
Download data: CEL, PDF
Series
Accession:
GSE6011
ID:
200006011
19.
Full record GDS3027

Early-early stage Duchenne muscular dystrophy: quadriceps

Analysis of skeletal muscles from 1.5 to 61 month old children with Duchenne muscular dystrophy (DMD). DMD is a degenerative skeletal muscle disease caused by mutations in the dystrophin gene. Results provide insight into the early phases of DMD pathogenesis and pathophysiology.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 22 age, 2 disease state, 2 gender sets
Platform:
GPL96
Series:
GSE6011
37 Samples
Download data: CEL
DataSet
Accession:
GDS3027
ID:
3027
20.

Molecular profiles (HG-U95A) of dystrophin-deficient and normal human muscle

(Submitter supplied) Molecular profiles of dystophin-deficient patients and normal human skeletal muscles on Affymetrix HG-U95A arrays Keywords = DMD Keywords = Duchenne muscular dystrophy Keywords = dystrophin Keywords = Affymetrix U95A array Keywords = skeletal muscle Keywords = gene expression profiles Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS563
Platforms:
GPL8300 GPL91
24 Samples
Download data: CEL, EXP, RPT
Series
Accession:
GSE1004
ID:
200001004
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