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GenomicsH3K9ac ChIP-seq profiling of wild-type and Slc31a1 conditional knockout mouse bone marrow stromal cells
H3K9ac ChIP-seq profiling of wild-type and Slc31a1 conditional knockout mouse bone marrow stromal cells
PRJNA1484612 | ENA
GenomicsH3K9ac ChIP-seq profiling of wild-type and Slc31a1 conditional knockout mouse bone marrow stromal cells
Age-associated bone loss is largely driven by impaired osteoblast generation from bone marrow stromal cells (BMSCs), but the metabolic and epigenetic mechanisms that regulate osteogenic commitment remain incompletely understood. This study identifies SLC31A1-mediated copper uptake as a cell-intrinsi...
ORGANISM(S): Mus musculus 
2026-07-31 | GSE337269 | GEO
GenomicsEffect of Slc31a1 deletion on gene expression of Lin-Sca1+c-Kit cell in the bone marrow of mice
Effect of Slc31a1 deletion on gene expression of Lin-Sca1+c-Kit cell in the bone marrow of mice
PRJNA1150545 | ENA
GenomicsChromatin accessibility profiling of wild-type and Slc31a1 conditional knockout mouse bone marrow stromal cells by ATAC-seq
Chromatin accessibility profiling of wild-type and Slc31a1 conditional knockout mouse bone marrow stromal cells by ATAC-seq
PRJNA1484604 | ENA
ProteomicsProteomic analysis of HoxB8-derived macrophages in which the Slc31a1 or Atp7a genes were inactivated using CRISPR/Cas9
This project is part of a study aimed at elucidating how Mycobacterium tuberculosis responds to physiologically relevant copper levels during macrophage infection. Here, we conducted a proteomic analysis of macrophages derived from immortalized HoxB8 hematopoietic precursors, in which the Slc31a1 (e...
ORGANISM(S): Mus musculus (Mouse) 
2026-08-25 | PXD076718 | Pride
Copper receptors Atp7a Slc31a1 Macrophages 
TranscriptomicsEffect of Slc31a1 deletion on gene expression of Lin-Sca1+c-Kit cell in the bone marrow of mice
Copper homeostasis has been linked to human health and hematopoiesis. However, the underlying mechanisms remain elusive. Here, we demonstrate the pivotal role of the transporter Slc31a1(Ctr1) in copper uptake, during postnatal hematopoiesis. Specifically, Slc31a1-mediated copper transport sustains t...
ORGANISM(S): Mus musculus 
2025-12-31 | GSE275365 | GEO
UnknownCuproptosis-related gene SLC31A1: prognosis values and potential biological functions in cancer.
Not available
S-EPMC10584849 | biostudies-literature
UnknownSystematic pan-cancer analysis identifies SLC31A1 as a biomarker in multiple tumor types.
Not available
S-EPMC10041742 | biostudies-literature
GenomicsChromatin accessibility profiling of wild-type and Slc31a1 conditional knockout mouse bone marrow stromal cells by ATAC-seq
Age-associated bone loss is largely driven by impaired osteoblast generation from bone marrow stromal cells (BMSCs), but the metabolic and epigenetic mechanisms that constrain osteogenic commitment remain incompletely understood. This study identifies SLC31A1-mediated copper uptake as a cell-intrins...
ORGANISM(S): Mus musculus 
2026-07-31 | GSE337266 | GEO
UnknownRole of SLC31A1 in prognosis and immune infiltration in breast cancer: a novel insight.
Not available
S-EPMC11558315 | biostudies-literature
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