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[PDF] Top 20 Immune regulation in IgA nephropathy

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Immune regulation in IgA nephropathy

Immune regulation in IgA nephropathy

... Fourty years after the fi rst description by Berger, the pathogenesis of this disease is still not resolved. Generally patients develop IgAN in their early twenties, however it may also become obvious later in life. Men ... See full document

168

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

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

... capture ELISA, flat-bottom, 96-well plates were coated at 4°C overnight with F(ab’)2 fragment of goat anti-human IgA antibody (Jackson ImmunoResarch Laboratories, West Grove, PA, USA) at a concentration of 2.5 ... See full document

14

A Study of mycophenolate and steroids in IGA nephropathy.

A Study of mycophenolate and steroids in IGA nephropathy.

... Use of new tissue markers of prognosis, such as those which can be obtained by special immunohistochemical studies for examining deposition of specific proteins (such as fibroblast specific protein-1), in-situ ... See full document

109

The coincidence of IgA nephropathy and Fabry disease

The coincidence of IgA nephropathy and Fabry disease

... The detection of a high level of autoantibodies has been found in patients with FD [10]. However, specific link between IgAN and FD has not yet been disclosed. It has been suggested that glycosphingolipids accumulating ... See full document

7

The level of urinary semaphorin3A is associated with disease activity in patients with minimal change nephrotic syndrome

The level of urinary semaphorin3A is associated with disease activity in patients with minimal change nephrotic syndrome

... organogenesis, immune responses and ...the regulation of the kidney development and ...n=22), IgA nephritis (n=21), membranous nephropathy (n=16) and focal segmental glomerular scle- rosis ... See full document

8

Urinary miRNA profile for the diagnosis of IgA nephropathy

Urinary miRNA profile for the diagnosis of IgA nephropathy

... of IgA nephropathy, we did not explore – and there may not be any – biological role of the miRNAs that we ...with IgA vasculitis, so that a risk stratification based on urinary miRNA level is not ... See full document

8

Race/ethnicity and disease severity in IgA nephropathy

Race/ethnicity and disease severity in IgA nephropathy

... asymptomatic IgA deposits is transplanted into a recipient with ESRD secondary to a disease other than IgAN, the IgA immune deposits in the donor kidney are rapidly removed ... See full document

6

Pathogenetic aspects of IgA-nephropathy

Pathogenetic aspects of IgA-nephropathy

... humans IgA is the predominant isotype produced (±66mg/kg/day), with 80 % of all B cells committed to IgA production ...of IgA (FcαR) have been identified on a variety of cell types within the ... See full document

18

Primary IgA nephropathy: current challenges and future prospects

Primary IgA nephropathy: current challenges and future prospects

... Abstract: IgA nephropathy (IgAN) is the most common form of primary glomerulonephritis worldwide, exhibiting a variable clinical and pathological course and significantly contributing to the global burden ... See full document

12

Recurrent Diffuse Alveolar Haemorrhage in a Patient with IgA Nephropathy Related End Stage Kidney Disease: A Rare Complication

Recurrent Diffuse Alveolar Haemorrhage in a Patient with IgA Nephropathy Related End Stage Kidney Disease: A Rare Complication

... was at this time that a need was felt for more aggressive immunosuppression for the immune mediated DAH. Seven sessions of plasmapheresis along with two doses of rituximab (375 milligram per meter square of body ... See full document

6

Histopathological assessment of prognosis of IGA nephropathy.

Histopathological assessment of prognosis of IGA nephropathy.

... polymeric IgA RR Fc alpha complexes that are deposited in the ...to immune complexes IgA1 polymeric-IgG. This macromolecular and immune complex persists in the ... See full document

84

Astragalus membranaceus up regulate Cosmc expression and reverse IgA dys glycosylation in IgA nephropathy

Astragalus membranaceus up regulate Cosmc expression and reverse IgA dys glycosylation in IgA nephropathy

... Astragalus membranaceus (AM) is a traditional Chinese herb, which is widely used in treating various renal diseases, including IgAN [4,5]. Many studies demonstrated to that AM have therapeutic effects on reducing ... See full document

7

The genetics and immunobiology of IgA nephropathy

The genetics and immunobiology of IgA nephropathy

... Thus, significant progress has been made in defining the role of IgA1 O-glycosylation in IgAN pathogenesis; evidence demon- strates that Gd-IgA1 originates from IgA1-secreting cells, and clinical studies have validated ... See full document

9

Circulating immune complexes in IgA nephropathy consist of IgA1 with galactose deficient hinge region and antiglycan antibodies

Circulating immune complexes in IgA nephropathy consist of IgA1 with galactose deficient hinge region and antiglycan antibodies

... A number of microorganisms, including viruses (e.g., respiratory syncitial, Epstein-Barr, and herpes viruses; refs. 39–41) and bacteria (certain strains of streptococ- ci; ref. 42), express GalNAc on their surface ... See full document

10

Pathogenic role of (S)IgA in IgA nephropathy

Pathogenic role of (S)IgA in IgA nephropathy

... To our best knowledge, data from the present study are the first indication for a role of L-ficolin in disease. In vitro data indicate that ligand specificities of MBL and L-ficolin do only partially overlap (16,17,48). ... See full document

144

IgA Nephropathy may be a Disease Related to Crohn's Disease

IgA Nephropathy may be a Disease Related to Crohn's Disease

... IgA nephropathy (IgAN) is the most common type of primary glomerulonephritis worldwide [1]. Clinical features vary from asymptomatic hematuria to nephrotic syndrome [1,2]. Prognosis is also varied. ... See full document

6

Early pre-eclampsia unmasks underlying IgA nephropathy

Early pre-eclampsia unmasks underlying IgA nephropathy

... The patient in this case report had fulfilled the criterion where the results of a renal biopsy had critical clinical consequences. There was histologic evidence of both pre- eclampsia and IgA nephropathy. ... See full document

5

IgA Nephropathy: A Malaysian Experience

IgA Nephropathy: A Malaysian Experience

... IgA Nephropathy A Malaysian Experience Med J Malaysia Vol 41 No 2 June 1986 IGA NEPHROPATHY A MALAYSIAN EXPERIENCE CHEONG I K s PHANG K s ABU BAKAR SULEIMAN ZAKIMORAD KONG B C T SUMMARY A total of 45[.] ... See full document

5

Mesangial cells from patients with IgA nephropathy have increased susceptibility to galactose-deficient IgA1

Mesangial cells from patients with IgA nephropathy have increased susceptibility to galactose-deficient IgA1

... In this study, we have shown that it is possible to harvest and to culture primary mesangial cells from renal biop- sies patients with for example IgAN and to study those cells in vitro. Our hypothesis was that the ... See full document

11

Selective deposition of immunoglobulin A1 in immunoglobulin A nephropathy, anaphylactoid purpura nephritis, and systemic lupus erythematosus

Selective deposition of immunoglobulin A1 in immunoglobulin A nephropathy, anaphylactoid purpura nephritis, and systemic lupus erythematosus

... the IgA deposits found in glomeruli of patients with IgA nephropathy, anaphylactoid purpura nephritis, and systemic lupus erythematosus, renal biopsies from patients with these disorders were stained ... See full document

6

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