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galactose-deficient iga1 (140) 140
index medicus (100) 100
humans (93) 93
iga nephropathy (85) 85
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glomerulonephritis (26) 26
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aberrantly glycosylated iga1 (25) 25
biopsy (24) 24
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henoch-schonlein purpura (20) 20
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human serum iga1 (17) 17
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glomerulonephritis, iga - etiology (15) 15
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autoantibodies (14) 14
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immunoglobulin a nephropathy (14) 14
risk factors (14) 14
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galactose - deficiency (11) 11
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iga1-containing immune-complexes (11) 11
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Journal Article
MOLECULAR & CELLULAR PROTEOMICS, ISSN 1535-9476, 11/2010, Volume 9, Issue 11, pp. 2545 - 2557
IgA nephropathy (IgAN) is the most common primary glomerulonephritis in the world. Aberrantly glycosylated IgA1, with galactose (Gal)-deficient hinge region... 
IMMUNE-COMPLEXES | RESONANCE MASS-SPECTROMETRY | ABERRANTLY GLYCOSYLATED IGA1 | HINGE REGION | ELECTRON-CAPTURE DISSOCIATION | HUMAN SERUM IGA1 | BIOCHEMICAL RESEARCH METHODS | GALACTOSE-DEFICIENT IGA1 | POSTTRANSLATIONAL MODIFICATIONS | NEPHROPATHY PATIENTS | PROTEINS
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 03/2019, Volume 81, Issue 5, pp. 1078 - 1085
IgA-vasculitis (IgAV) encompasses a systemic form involving kidneys, gut, skin or joints, and a skin-limited form. One characteristic feature of systemic IgAV... 
Enzymes | Vasculitis | Analysis | Skin care products | Skin | Kidney diseases | Galactose | Immunoglobulin A | Enzyme-linked immunosorbent assay
Journal Article
Journal Article
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 12/2012, Volume 82, Issue 12, pp. 1284 - 1296
IgA nephropathy (IgAN), the most common primary glomerulonephritis worldwide, has significant morbidity and mortality as 20–40% of patients progress to... 
IgA deposition | IgA | IgA nephropathy | KIDNEY-DISEASE | POLYMERIC IGA1 | MONOCYTE CHEMOATTRACTANT PROTEIN-1 | FACTOR-KAPPA-B | ABERRANT GLYCOSYLATION | PREDICTING PROGRESSION | RESONANCE MASS-SPECTROMETRY | TRANSFERRIN RECEPTOR | HINGE REGION | GALACTOSE-DEFICIENT IGA1 | UROLOGY & NEPHROLOGY | Blood Pressure | Antigen-Antibody Complex | Phosphorylation | Cell Proliferation | TOR Serine-Threonine Kinases - metabolism | Calcium - metabolism | Humans | Middle Aged | Glomerulonephritis, IGA - immunology | Podocytes - enzymology | Male | Extracellular Signal-Regulated MAP Kinases - metabolism | Angiotensin II Type 1 Receptor Blockers - pharmacology | Antigens, CD - metabolism | Mesangial Cells - drug effects | Glomerulonephritis, IGA - enzymology | Young Adult | Angiotensin-Converting Enzyme Inhibitors - therapeutic use | Renin-Angiotensin System | Time Factors | Inflammation Mediators - metabolism | Mesangial Cells - enzymology | Adult | Female | Proto-Oncogene Proteins c-akt - metabolism | Interleukin-6 - metabolism | Phosphatidylinositol 3-Kinase - metabolism | Glomerulonephritis, IGA - pathology | Glomerulonephritis, IGA - physiopathology | Immunoglobulin A - metabolism | Angiotensin II - metabolism | Proteinuria - immunology | Mesangial Cells - immunology | Cells, Cultured | Podocytes - pathology | Receptors, Transferrin - metabolism | Proteinuria - enzymology | MAP Kinase Signaling System - drug effects | Podocytes - drug effects | Biopsy | Podocytes - immunology | Cell Communication - drug effects | Mesangial Cells - pathology | Aged | Enzyme Activation | Glomerulonephritis | End-stage renal disease | Renal function | Cytokines | Immunoglobulin G | Mortality | Extracellular signal-regulated kinase | MAP kinase | Inflammation | Morbidity | Signal transduction | Molecular modelling | Mesangial cells | Blood pressure | Antigen-antibody complexes | Mesangium | Proteinuria
Journal Article
Seminars in Nephrology, ISSN 0270-9295, 09/2018, Volume 38, Issue 5, pp. 461 - 476
IgA nephropathy, the most common primary glomerulonephritis in the world and a frequent cause of end-stage renal disease, is characterized by typical mesangial... 
autoantibody | signaling | IgA1 | O-glycans | HUMAN SERUM IGA1 | SECRETORY IGA | IMMUNOGLOBULIN-A NEPHROPATHY | O-LINKED OLIGOSACCHARIDES | FLIGHT MASS-SPECTROMETRY | HUMAN MESANGIAL CELLS | OXFORD CLASSIFICATION | GALACTOSE-DEFICIENT IGA1 | IGA1-CONTAINING IMMUNE-COMPLEXES | UROLOGY & NEPHROLOGY | HINGE-REGION
Journal Article
Seminars in Immunopathology, ISSN 1863-2297, 05/2012, Volume 34, Issue 3, pp. 365 - 382
Journal Article
Kidney International, ISSN 0085-2538, 10/2012, Volume 82, Issue 7, pp. 790 - 796
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 05/2008, Volume 19, Issue 5, pp. 1008 - 1014
Journal Article