Sort   by:  
 Page size 
ProteomicsSerum proteomic analysis of circulating IgA1-containing immune complexes in patients with IgA nephropathy
IgA nephropathy (IgAN) is an autoimmune disease that involves galactose-deficient IgA1 (Gal-deficient IgA1) recognized by autoantibodies to form circulating immune complexes (IgA1-IC). Some of these complexes deposit in the glomeruli and induce kidney injury. Gal-deficient IgA1 alone is not sufficie...
ORGANISM(S): Homo sapiens (Human) 
2025-11-03 | PXD055562 | Pride
Proteomics Lc-ms Complement Orbitrap Raw Immune complexes Serum Iga nephropathy Glomerular disease 
UnknownDistinct metabolic programs established in the thymus control effector functions of γδ T cell subsets in tumor microenvironments.
Not available
S-EPMC7610600 | biostudies-literature
UnknownThe Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources.
Not available
S-EPMC7613247 | biostudies-literature
UnknownTowards robust clinical genome interpretation: developing a consistent terminology to characterize disease-gene relationships - allelic requirement, inheritance modes and disease mechanisms.
Not available
S-EPMC10104222 | biostudies-literature
GenomicsWP8_DNA_Methylation_450K_UCL
BLUEPRINT DNA methylation profiles of monocytes, T cells and B cells in type 1 diabetes-discordant monozygotic twins
EGAD00010001025 | EGA
Genomicsena-DATASET-BLUEPRINT-13-09-2016-12:21:58:649-53 - samples
BLUEPRINT DNA methylation profiles of monocytes, T cells and B cells in type 1 diabetes-discordant monozygotic twins (Bisulfite-Seq data).
EGAD00001002682 | EGA
GenomicsBLUEPRINT DNA methylation profiles of monocytes, T cells and B cells in type 1 diabetes-discordant monozygotic twins
BLUEPRINT DNA methylation profiles of monocytes, T cells and B cells in type 1 diabetes-discordant monozygotic twins
EGAS00001001598 | EGA
UnknownMethods for high-dimensional analysis of cells dissociated from cryopreserved synovial tissue
Not available
S-EPMC6042350 | biostudies-literature
UnknownAltered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study.
Not available
S-EPMC6986984 | biostudies-literature
UnknownAn ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.
Not available
S-EPMC8263055 | biostudies-literature
Sort   by:  
 Page size