Results 61 to 70 of about 356,021 (162)
Galactose-Deficient IgA1 as a Candidate Urinary Polypeptide Marker of IgA Nephropathy? [PDF]
In patients with IgA nephropathy (IgAN), circulatory IgA1 and IgA1 in mesangial deposits contain elevated amounts of galactose-deficient IgA1 (Gd-IgA1). We hypothesized that a fraction of Gd-IgA1 from the glomerular deposits and/or circulation may be excreted into the urine and thus represent a disease-specific biomarker.
Hitoshi Suzuki +7 more
openaire +2 more sources
Dotplot showing individual serum galactose deficient IgA1 values in all three groups.
Dotplot showing individual serum galactose deficient IgA1 values in all three groups.
Geetika Singh (6519728) +7 more
core +1 more source
Using Synthetic Glycans to Investigate Anti‐Glycan Antibodies and Explore Their Medical Potential
Anti‐glycan antibodies are essential in health and disease. Access to novel glycan structures paves the way for progress in antibody profiling for biomarker discovery, antibody development, and vaccine design. We summarize the strategies to synthesize and utilize synthetic glycans for the development and application of anti‐glycan antibodies in basic ...
Fabienne Weber +4 more
wiley +1 more source
Comparison of serum galactose deficient IgA1 levels between non-IgA glomerular disease subtypes and Iga nephropathy.
Geetika Singh (6519728) +7 more
core +1 more source
Experimental IgA nephropathy leads to renal inflammation, fibrosis, podocyte injury, and impaired renal function. Sarsasapogenin treatment attenuated inflammatory and profibrotic signaling, reduced extracellular matrix accumulation, preserved nephrin and podocin expression, improved podocyte ultrastructure, and ameliorated renal histopathological ...
Meltem Kumaş +7 more
wiley +1 more source
Diagnostic value of BTG2 and its immunoregulatory mechanism in IgAN. This study reveals that BTG2 improves immune microenvironment dysregulation, attenuates inflammation, and reduces fibrosis by promoting the expansion of T follicular helper cells, inducing macrophage polarization toward an M2 anti‐inflammatory phenotype, and inhibiting the TGF‐β1 ...
Min Kou +4 more
wiley +1 more source
A ROC curve of serum galactose deficient IgA1 level against IgA nephropathy patients and healthy controls 2B ROC cure of serum galactose deficienty IgA1 level against IgA nephropathy patients and non-IgA glomerular disease controls.
Geetika Singh (6519728) +7 more
core +1 more source
Serum galactose‐deficient IgA1 levels at 3 and 6 months predicted recurrent IgA nephropathy after kidney transplantation. Recipients without recurrence showed a rapid decline in galactose‐deficient IgA1 after transplantation. Early identification of recurrence risk provided a potential window for targeted post‐transplant intervention.
Ronghai Deng +10 more
wiley +1 more source
Diagnosis and treatment of patients with IgA nephropathy in Japan
Chronic kidney disease (CKD) is a worldwide public health problem that affects millions of people from all racial and ethnic groups. Although CKD is not one specific disease, it is a comprehensive syndrome that includes IgA nephropathy.
Yasuhiko Tomino
doaj +1 more source
Histogram showing distribution of values of serum galactose deficient IgA1(ng/ml) before(4A) and after(4B) logarithmic transformation.
Geetika Singh (6519728) +7 more
core +1 more source

