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Comparison of wild-type and mutant H3.3 and histone H3 modifications between H3F3A mutant and wild-type GCTB stromal cells.
ORGANISM(S): Homo sapiens 
Analysis of chromatin accessibility in primary GCTB samples with ATAC-seq
ORGANISM(S): Homo sapiens 
Background: Low birth weight is associated with an increased adult metabolic disease risk. It is widely discussed that poor intrauterine conditions could induce long-lasting epigenetic modifications, leading to systemic changes in regulation of metabolic genes. In a unique cohort of 17 monozygotic (...
ORGANISM(S): Homo sapiens 
Single-end BAM files of the targeted deep sequencing analysis of several mtDNA candidate regions in blood and buccal-derived DNA of the corresponding twin pairs.
Paired-end BAM files of mitochondrial whole genome deep sequencing (mtWGDS) analysis
paired-end BAM files of the sequencing analysis of the mtDNA polymerase gamma (POLG) gene in the MS-affected co-twins
Several lines of evidence indicate that mitochondrial DNA (mtDNA) variants might predispose to multiple sclerosis (MS). We examined this in 49 monozygotic (MZ) twin pairs clinically discordant for MS at study entry. Since the nuclear DNA of MZ twins is identical, our study provides a unique setting ...
Data Access Committee EGAC00001000331
McGill EMC Release 4 for assay "H3K9me3"
McGill EMC Release 4 in tissue "venous blood" for cell type "CD4-positive helper T cell"
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