Similar studies for GEO DataSets (Select 638) - GEO DataSets

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Items: 20

Select item 6381.

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 2000010262.

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 2000032523.

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

Select item 17784.

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

Select item 2000010085.

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

Select item 6146.

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

Select item 2000010257.

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

Select item 6398.

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

Select item 2000021129.

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

Select item 20000089710.

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

Select item 64111.

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

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 20000046614.

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

Select item 23615.

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

Select item 20003566116.

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 20000157417.

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 20000601118.

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

Select item 302719.

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

Select item 20000100420.

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