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TranscriptomicsTranscription profiling of human Facioscapulohumeral muscular dystrophy (FSHD) muscle profiles
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disorder linked to contractions of the D4Z4 repeat array in the subtelomeric region of chromosome 4q. By comparing genome-wide gene expression data from muscle biopsies of patients with FSHD to those of 11 other neuromuscular dis...
ORGANISM(S): Homo sapiens 
2008-06-16 | E-GEOD-9397 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of heart from Lmna H222P homozygous and control mice
The present research is devoted to the identification of gene(s) severely affected by LMNA mutations, leading to striated muscle laminopathies and more specifically the cardiomyopathy. For this purpose, we developped a large-scale gene expression approach on heart and skeletal tissues from Lmna H222...
ORGANISM(S): Mus musculus 
2008-06-14 | E-GEOD-6398 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of mouse heart samples from individuals with homozygous or heterozygous mutant alleles of Lamin A (LMNA)
This SuperSeries is composed of the following subset Series:; GSE6397: Comparison between gene expression in heart from Lmna H222P heterozygous and control mice; GSE6398: Comparison between gene expression in heart from Lmna H222P homozygous and control mice Experiment Overall Design: Refer to indiv...
ORGANISM(S): Mus musculus 
2007-10-31 | E-GEOD-8000 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of mouse heart from Lmna H222P heterozygous and control mice
The present research is devoted to the identification of gene(s) severely affected by LMNA mutations, leading to striated muscle laminopathies and more specifically the cardiomyopathy. For this purpose, we developped a large-scale gene expression approach on heart and skeletal tissues from Lmna H222...
ORGANISM(S): Mus musculus 
2008-06-14 | E-GEOD-6397 | biostudies-arrayexpress
TranscriptomicsComparative profiling in 13 muscle disease groups
Summary: Genetic disorders of muscle cause muscular dystrophy, and are some of the most common inborn errors of metabolism. Muscle also rapidly remodels in response to training and innervation. Muscle weakness and wasting is important in such conditions as aging, critical care medicine, space flig...
ORGANISM(S): Homo sapiens 
2005-10-14 | E-GEOD-3307 | biostudies-arrayexpress
GenomicsWhole genome miRNA analysis of in-vitro differentiated myotubes from Emery-Dreifuss Muscular Dystrophy patients.
Whole genome miRNA analysis of in-vitro differentiated myotubes from Emery-Dreifuss Muscular Dystrophy patients.
PRJNA842409 | ENA
UnknownA multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism.
Not available
S-EPMC7000448 | biostudies-literature
GenomicsTranscriptome analysis of in-vitro differentiated myotubes from Emery-Dreifuss Muscular Dystrophy patients.
Transcriptome analysis of in-vitro differentiated myotubes from Emery-Dreifuss Muscular Dystrophy patients.
PRJNA842374 | ENA
UnknownClinical aspects of Emery-Dreifuss muscular dystrophy.
Not available
S-EPMC5973255 | biostudies-literature
UnknownProfibrotic Molecules Are Reduced in CRISPR-Edited Emery-Dreifuss Muscular Dystrophy Fibroblasts.
Not available
S-EPMC12427866 | biostudies-literature
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