Pages that link to "Q36303703"
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The following pages link to IgA1-secreting cell lines from patients with IgA nephropathy produce aberrantly glycosylated IgA1 (Q36303703):
Displaying 50 items.
- The Origin and Activities of IgA1-Containing Immune Complexes in IgA Nephropathy (Q26752555) (← links)
- New developments in the genetics, pathogenesis, and therapy of IgA nephropathy (Q26786248) (← links)
- Genetic studies of IgA nephropathy: what have we learned from genome-wide association studies (Q26829467) (← links)
- The pathophysiology of IgA nephropathy (Q27023866) (← links)
- The kinetics of glomerular deposition of nephritogenic IgA (Q27325252) (← links)
- Enzymatic sialylation of IgA1 O-glycans: implications for studies of IgA nephropathy (Q28539595) (← links)
- Expression and glycoengineering of functionally active heteromultimeric IgM in plants (Q30412932) (← links)
- Severe transient ADAMTS13 deficiency in pneumococcal-associated hemolytic uremic syndrome (Q33393302) (← links)
- Development of IgA nephropathy-like glomerulonephritis associated with Wiskott-Aldrich syndrome protein deficiency (Q33398196) (← links)
- Allogeneic bone marrow transplantation appears to ameliorate IgA nephropathy in a patient with X-linked thrombocytopenia (Q33411395) (← links)
- A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases (Q33654763) (← links)
- Serum under-O-glycosylated IgA1 level is not correlated with glomerular IgA deposition based upon heterogeneity in the composition of immune complexes in IgA nephropathy (Q33780876) (← links)
- The combined role of galactose-deficient IgA1 and streptococcal IgA-binding M Protein in inducing IL-6 and C3 secretion from human mesangial cells: implications for IgA nephropathy (Q33787385) (← links)
- Comparison of methods for profiling O-glycosylation: Human Proteome Organisation Human Disease Glycomics/Proteome Initiative multi-institutional study of IgA1 (Q33812834) (← links)
- The genetics and immunobiology of IgA nephropathy (Q33872517) (← links)
- Genetic studies of IgA nephropathy: past, present, and future. (Q34109845) (← links)
- Genetics and immunopathogenesis of IgA nephropathy (Q34156795) (← links)
- Suppression of adiponectin by aberrantly glycosylated IgA1 in glomerular mesangial cells in vitro and in vivo. (Q34212088) (← links)
- Clustered O-glycans of IgA1: defining macro- and microheterogeneity by use of electron capture/transfer dissociation. (Q34320745) (← links)
- Serum levels of galactose-deficient immunoglobulin (Ig) A1 and related immune complex are associated with disease activity of IgA nephropathy (Q34324220) (← links)
- Down-regulation of core 1 beta1,3-galactosyltransferase and Cosmc by Th2 cytokine alters O-glycosylation of IgA1. (Q34340715) (← links)
- Identification of distinct glycoforms of IgA1 in plasma from patients with immunoglobulin A (IgA) nephropathy and healthy individuals (Q34468379) (← links)
- Increased plasma sVCAM-1 is associated with severity in IgA nephropathy (Q34556089) (← links)
- Aberrantly glycosylated IgA1 as a factor in the pathogenesis of IgA nephropathy (Q34557198) (← links)
- Aberrantly glycosylated IgA1 in IgA nephropathy patients is recognized by IgG antibodies with restricted heterogeneity (Q34608317) (← links)
- Comprehensive human urine standards for comparability and standardization in clinical proteome analysis (Q34725022) (← links)
- N-acetylgalactosaminide α2,6-sialyltransferase II is a candidate enzyme for sialylation of galactose-deficient IgA1, the key autoantigen in IgA nephropathy (Q35022256) (← links)
- DNA methylation in Cosmc promoter region and aberrantly glycosylated IgA1 associated with pediatric IgA nephropathy (Q35043308) (← links)
- Different pathological roles of toll-like receptor 9 on mucosal B cells and dendritic cells in murine IgA nephropathy (Q35101639) (← links)
- Changes in nephritogenic serum galactose-deficient IgA1 in IgA nephropathy following tonsillectomy and steroid therapy (Q35107938) (← links)
- Development of Animal Models of Human IgA Nephropathy (Q35110061) (← links)
- Oxidative stress and galactose-deficient IgA1 as markers of progression in IgA nephropathy (Q35165506) (← links)
- Immune profile of IgA-dominant diffuse proliferative glomerulonephritis. (Q35232158) (← links)
- IgA1 immune complexes from pediatric patients with IgA nephropathy activate cultured human mesangial cells (Q35468711) (← links)
- Galectin-8 in IgA nephritis: decreased binding of IgA by galectin-8 affinity chromatography and associated increased binding in non-IgA serum glycoproteins. (Q35834840) (← links)
- A proton nuclear magnetic resonance-based metabonomics study of metabolic profiling in immunoglobulin a nephropathy. (Q35864994) (← links)
- Novel lectin-independent approach to detect galactose-deficient IgA1 in IgA nephropathy (Q35886028) (← links)
- Promoters of Human Cosmc and T-synthase Genes Are Similar in Structure, Yet Different in Epigenetic Regulation (Q35905327) (← links)
- Abnormal miR-148b expression promotes aberrant glycosylation of IgA1 in IgA nephropathy (Q35917473) (← links)
- Autoantibodies targeting galactose-deficient IgA1 associate with progression of IgA nephropathy (Q36200922) (← links)
- The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression (Q36237466) (← links)
- New Insights into the Pathogenesis of IgA Nephropathy (Q36267833) (← links)
- GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway (Q36276884) (← links)
- Determination of severity of murine IgA nephropathy by glomerular complement activation by aberrantly glycosylated IgA and immune complexes (Q36295467) (← links)
- Epigenetic silencing of the chaperone Cosmc in human leukocytes expressing tn antigen (Q36436153) (← links)
- IgA glycosylation and IgA immune complexes in the pathogenesis of IgA nephropathy (Q36456627) (← links)
- A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy (Q36695721) (← links)
- Production of N-acetylgalactosaminyl-transferase 2 (GalNAc-T2) fused with secretory signal Igκ in insect cells (Q36797332) (← links)
- Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch-Schönlein purpura nephritis (Q36810321) (← links)
- Sialic acids in human health and disease (Q36908164) (← links)