Similar studies for GEO DataSets (Select 563) - GEO DataSets

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Items: 20

Select item 5631.

Duchenne muscular dystrophy (II) (HG-U95A)

Search for modifying factors and pathogenic pathways involved in Duchenne muscular dystrophy (DMD). Quadricep skeletal muscle biopsies from 12 DMD patients and 11 unaffected control patients examined.

Organism:: Homo sapiens

Type:: Expression profiling by array, count, 2 disease state sets

Platform:: GPL8300
Series:: GSE1004
23 Samples

Download data: CEL, EXP, RPT

DataSet

Accession:: GDS563

ID:: 563

PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet

Select item 2000010042.

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

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 2000010073.

Molecular profiles(HG-U95B,C,D,E) of dystrophin-deficient and normal human skeletal muscle

(Submitter supplied) molecular profiles (HG-U95B,C,D,E) of biopsy skeletal muscle samples obtained from 10 normal individuals and 10 DMD patients Keywords = gene expression profiles of normal human skeletal muscles Keywords = gene expression profiles of DMD patients' skelatal muscle samples Keywords = Affymetrix HG-U95B Keywords = Affymetrix HG-U95C Keywords = Affymetrix HG-U95D Keywords = Affymetrix HG-U95E Keywords: other

Organism:: Homo sapiens

Type:: Expression profiling by array

Datasets:: GDS609 GDS610 GDS611 GDS612
4 related Platforms
86 Samples

Download data: CEL, EXP, RPT

Series

Accession:: GSE1007

ID:: 200001007

Select item 6124.

Duchenne muscular dystrophy (II) (HG-U95E)

Search for modifying factors and pathogenic pathways involved in Duchenne muscular dystrophy (DMD). Quadricep skeletal muscle biopsies from DMD patients and unaffected control patients examined.

Organism:: Homo sapiens

Type:: Expression profiling by array, count, 2 disease state sets

Platform:: GPL95
Series:: GSE1007
21 Samples

Download data: CEL, EXP, RPT

DataSet

Accession:: GDS612

ID:: 612

Select item 6115.

Duchenne muscular dystrophy (II) (HG-U95D)

Search for modifying factors and pathogenic pathways involved in Duchenne muscular dystrophy (DMD). Quadricep skeletal muscle biopsies from DMD patients and unaffected control patients examined.

Organism:: Homo sapiens

Type:: Expression profiling by array, count, 2 disease state sets

Platform:: GPL94
Series:: GSE1007
22 Samples

Download data: CEL, EXP, RPT

DataSet

Accession:: GDS611

ID:: 611

Select item 6106.

Duchenne muscular dystrophy (II) (HG-U95C)

Search for modifying factors and pathogenic pathways involved in Duchenne muscular dystrophy (DMD). Quadricep skeletal muscle biopsies from DMD patients and unaffected control patients examined.

Organism:: Homo sapiens

Type:: Expression profiling by array, count, 2 disease state sets

Platform:: GPL93
Series:: GSE1007
22 Samples

Download data: CEL, EXP, RPT

DataSet

Accession:: GDS610

ID:: 610

Select item 6097.

Duchenne muscular dystrophy (II) (HG-U95B)

Search for modifying factors and pathogenic pathways involved in Duchenne muscular dystrophy (DMD). Quadricep skeletal muscle biopsies from DMD patients and unaffected control patients examined.

Organism:: Homo sapiens

Type:: Expression profiling by array, count, 2 disease state sets

Platform:: GPL92
Series:: GSE1007
21 Samples

Download data: CEL, EXP, RPT

DataSet

Accession:: GDS609

ID:: 609

Select item 2000010268.

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

Select item 6389.

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

Select item 20003566110.

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

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 20000157411.

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

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 20000147212.

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

Select item 70313.

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

Select item 20000269314.

Time course Healthy DMD myogenesis

(Submitter supplied) Primairy human myoblast cell cultures Healthy DMD Keywords: time-course

Organism:: Homo sapiens

Type:: Expression profiling by array

Platform:: GPL2097
42 Samples

Download data

Series

Accession:: GSE2693

ID:: 200002693

Select item 20000176415.

Effect of Oxandrolone on Muscle in Duchenne Muscular Dystrophy

(Submitter supplied) Three subjects with Duchenne muscular dystrophy (8.3, 10.4, and 16.7 years old) were studied. Baseline studies included stable isotope infusion followed by gastrocnemius muscle biopsy to determine myosin heavy chain synthesis rates. RNA was isolated from the muscle biopsy as well. The subjects were then treated for 3 months with oxandrolone (a synthetic anabolic steroid, 0.1 mg/kg/day) and the studies repeated. more...

Organism:: Homo sapiens

Type:: Expression profiling by array

Datasets:: GDS1333 GDS1334
Platforms:: GPL96 GPL97
12 Samples

Download data

Series

Accession:: GSE1764

ID:: 200001764

Select item 133416.

Duchenne Muscular Dystrophy response to oxandrolone (HG-U133B)

Analysis of gastrocnemius muscle biopsy specimens from Duchenne muscular dystrophy (DMD) patients before and after 3 months of treatment with 0.1mg/kg/day oxandrolone, a synthetic anabolic steroid. Results provide insight into mechanisms underlying the beneficial effect of oxandrolone in DMD.

Organism:: Homo sapiens

Type:: Expression profiling by array, count, 2 agent, 3 individual sets

Platform:: GPL97
Series:: GSE1764
6 Samples

Download data

DataSet

Accession:: GDS1334

ID:: 1334

Select item 133317.

Duchenne Muscular Dystrophy response to oxandrolone (HG-U133A)

Organism:: Homo sapiens

Type:: Expression profiling by array, count, 2 agent, 3 individual sets

Platform:: GPL96
Series:: GSE1764
6 Samples

Download data

DataSet

Accession:: GDS1333

ID:: 1333

Select item 20015649818.

Degenerative and Regenerative Pathways Underlying Duchenne Muscular Dystrophy Revealed by Single-nucleus RNA sequencing

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.

Organism:: Mus musculus

Type:: Expression profiling by high throughput sequencing

Platform:: GPL19057
8 Samples

Download data: MTX, TSV

Series

Accession:: GSE156498

ID:: 200156498

PubMed Full text in PMC Similar studies

Select item 20015649719.

Single nucleus RNA-seq analysis of the TA muscles from WT and Dmd Exon 51 Knockout mice

(Submitter supplied) Duchenne muscular dystrophy (DMD) is a fatal muscle disorder characterized by cycles of degeneration and regeneration of multinucleated myofibers and pathological activation of a variety of other associated cell types. Here, we describe the creation of a new mouse model of DMD caused by deletion of exon 51 of the dystrophin gene, which represents a prevalent mutation in humans. To understand the transcriptional abnormalities and heterogeneity associated with the nuclei of myofibers, as well as other mononucleated cell types that contribute to DMD disease pathogenesis, we performed single nucleus transcriptomics of skeletal muscle of mice with exon 51 deletion. more...