Allelic variants of complement genes associated with dense deposit disease. - sprookjes - yvandenbroek - TriplyDB

Allelic variants of complement genes associated with dense deposit disease.

Allelic variants of complement genes associated with dense deposit disease.

http://www.wikidata.org/entity/Q35142753

about

The complotype: dictating risk for inflammation and infection Membranoproliferative glomerulonephritis and C3 glomerulopathy: resolving the confusion Genetic variants in the complement system predisposing to age-related macular degeneration: a review First-line therapy in atypical hemolytic uremic syndrome: consideration on infants with a poor prognosis Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency.C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up.Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN.Dense deposit disease.Crescentic acute glomerulonephritis with isolated C3 deposition: a case report and review of literature.Association of a novel complement factor H mutation with severe crescentic and necrotizing glomerulonephritis.Secondary focal and segmental glomerulosclerosis associated with single-nucleotide polymorphisms in the genes encoding complement factor H and C3.C3 glomerulonephritis associated with monoclonal gammopathy: a case series.Treatment options for C3 glomerulopathy Causes of alternative pathway dysregulation in dense deposit disease.Complement Dysregulation and Disease: Insights from Contemporary Genetics.Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement.The Genetics of Ultra-Rare Renal Disease.Dense deposit disease and C3 glomerulopathy C3 glomerulopathy: consensus report.C3 glomerulonephritis and CFHR5 nephropathy.Recent insights into C3 glomerulopathy Making sense of the spectrum of glomerular disease associated with complement dysregulation.Histopathology of MPGN and C3 glomerulopathies.Complementing the Sugar Code: Role of GAGs and Sialic Acid in Complement Regulation Eculizumab-induced reversal of dialysis-dependent kidney failure from C3 glomerulonephritis.C4 Nephritic Factors in C3 Glomerulopathy: A Case Series.Diseases of complement dysregulation-an overview.C3 glomerulonephritis with a severe crescentic phenotype.Functional Characterization of the Disease-Associated N-Terminal Complement Factor H Mutation W198R.C3 glomerulonephritis and autoimmune disease: more than a fortuitous association?In search of an effective treatment for recurrent mesangiocapillary glomerulonephritis in the renal allograft.C3 Glomerulopathy.Renal and Pulmonary Dense Deposit Disease Presenting as Pulmonary-Renal Syndrome.Analysis of C3 Gene Variants in Patients With Idiopathic Recurrent Spontaneous Pregnancy Loss

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P2860

Allelic variants of complement genes associated with dense deposit disease.

http://www.wikidata.org/entity/Q35142753

description

2011 nî lūn-bûn

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2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2011 թվականի հուլիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Allelic variants of complement genes associated with dense deposit disease.

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Allelic variants of complement genes associated with dense deposit disease.

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type

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Allelic variants of complement genes associated with dense deposit disease.

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Allelic variants of complement genes associated with dense deposit disease.

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Allelic variants of complement genes associated with dense deposit disease.

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Allelic variants of complement genes associated with dense deposit disease.

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Journal of the American Society of Nephrology

P1476

Allelic variants of complement genes associated with dense deposit disease.

@en

P2093

Carla Nishimura

http://www.w3.org/2001/XMLSchema#string

Kathy Frees

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Louis M Katz

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Maria Asuncion Abrera-Abeleda

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Michael Jones

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Richard J H Smith

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Tara Maga

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Yuzhou Zhang

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P2860

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome

Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)

Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome

Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)

Identification of a restriction fragment length polymorphism by a CR1 cDNA that correlates with the number of CR1 on erythrocytes

Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods

Structure shows that a glycosaminoglycan and protein recognition site in factor H is perturbed by age-related macular degeneration-linked single nucleotide polymorphism

Haploview: analysis and visualization of LD and haplotype maps

Nephritogenic lambda light chain dimer: a unique human miniautoantibody against complement factor H

Visual impairment caused by retinal abnormalities in mesangiocapillary (membranoproliferative) glomerulonephritis type II ("dense deposit disease")

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10.1681/ASN.2010080795

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8

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22

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