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Hutchinson-Gilford progeria syndrome: fibroblast (HG-U133B)
PubMed Similar studies GEO Profiles Analyze DataSet
Comparison of Hutchinson–Gilford Progeria Syndrome fibroblast cell lines to control fibroblast cell lines
PubMed Similar studies Analyze with GEO2R
Hutchinson-Gilford progeria syndrome: fibroblast (HG-U133A)
Comparative profiling in 13 muscle disease groups
PubMed Full text in PMC Similar studies Analyze with GEO2R
Various muscle diseases (HG-U133B)
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
Various muscle diseases (HG-U133A)
Epigenetic deregulation of lamina-associated domains in Hutchinson-Gilford Progeria Syndrome
PubMed Full text in PMC Similar studies
Epigenetic deregulation of lamina-associated domains in Hutchinson-Gilford Progeria Syndrome (RNA-Seq)
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
Epigenetic deregulation of lamina-associated domains in Hutchinson-Gilford Progeria Syndrome (ATAC-Seq)
PubMed Full text in PMC Similar studies SRA Run Selector
Reprogramming Hutchinson-Gilford Progeria Syndrome fibroblasts resets epigenomic landscape in patient-derived induced pluripotent stem cells [ChIP-Seq]
Quantitative whole transcriptomics sequencing of progeria-derived cells point to a key role of nucleotide metabolism in premature aging
Transcriptional profiling of liver samples from Lmna Gly609Gly knock-in mice
Lmna G609G knock-in model of Hutchinson-Gilford Progeria Syndrome: liver
Correlated alterations in genome organization, histone methylation, and DNA-lamina interactions in Hutchinson-Gilford progeria syndrome
Correlated alterations in genome organization, histone methylation, and DNA-lamina interactions in Hutchinson-Gilford progeria syndrome (Hi-C)
Correlated alterations in genome organization, histone methylation, and DNA-lamina interactions in Hutchinson-Gilford progeria syndrome (ChIP-seq)
Correlated alterations in genome organization, histone methylation, and DNA-lamina interactions in Hutchinson-Gilford progeria syndrome (expression)
Gene expression profiling of fibroblasts in a family with LMNA-related cardiomyopathy reveals molecular pathways implicated in disease pathogenesis
Aortas of mice on high fat diet
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