Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies (Q56908029)

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27 January 2020

title

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies (English)

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1

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Lubka T. Roumenina

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Moglie Le Quintrec

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Marie-Agnès Dragon-Durey

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Julien Zuber

8

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Bruno Moulin

11

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Véronique Frémeaux-Bacchi

27 January 2020

15

object named as

Véronique Frémeaux-Bacchi

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14

Philippe Lesavre

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2

Laure-Hélène Noël

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author name string

Stephanie Ngo

5

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Marie-Alice Macher

7

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Alexandre Karras

9

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François Provot

10

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Jean-Pierre Grünfeld

12

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Patrick Niaudet

13

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language of work or name

English

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publication date

28 March 2012

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27 January 2020

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volume

82

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issue

4

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page(s)

454-464

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https://scigraph.springernature.com/pub.10.1038/ki.2012.63

27 January 2020

exact match

0 references

cites work

Membranoproliferative glomerulonephritis type II (dense deposit disease): an update

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

C3 glomerulopathy: a new classification

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Dense deposit disease is not a membranoproliferative glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Glomeruli of Dense Deposit Disease contain components of the alternative and terminal complement pathway

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Heterogeneous pattern of renal disease associated with homozygous Factor H deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

MPGN II--genetically determined by defective complement regulation?

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

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)

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Complement factor H deficiency accelerates development of lupus nephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Structure of complement fragment C3b-factor H and implications for host protection by complement regulators

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Complement factor h gene abnormalities in haemolytic uraemic syndrome: from point mutations to hybrid gene

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Severity of primary MPGN, rather than MPGN type, determines renal survival and post-transplantation recurrence risk

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Idiopathic mesangiocapillary glomerulonephritis. Comparison of types I and II in children and adults and long-term prognosis

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Mesangiocapillary glomerulonephritis: A long-term study of 40 cases

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

The prognostic value of some clinical and histological parameters in membranoproliferative glomerulonephritis (MPGN): report of 112 cases

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Complement analysis in children with idiopathic membranoproliferative glomerulonephritis: a long-term follow-up

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Prognostic factors in mesangioproliferative glomerulonephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Protection of the classical and alternative complement pathway C3 convertases, stabilized by nephritic factors, from decay by the human C3b receptor

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

His-384 Allotypic Variant of Factor H Associated with Age-related Macular Degeneration Has Different Heparin Binding Properties from the Non-disease-associated Form

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Defective complement control of factor H (Y402H) and FHL-1 in age-related macular degeneration

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https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Lessons from functional and structural analyses of disease-associated genetic variants in the complement alternative pathway.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Alternative complement pathway assessment in patients with atypical HUS.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Definition and classification of chronic kidney disease: a position statement from Kidney Disease: Improving Global Outcomes (KDIGO).

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

A simple estimate of glomerular filtration rate in full-term infants during the first year of life

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https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

A simple estimate of glomerular filtration rate in adolescent boys.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2012.63

7 January 2021

Identifiers

DOI

10.1038/KI.2012.63

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22456601%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

1 reference