(Q33396948)

English

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

atypical hemolytic uremic syndrome

1 reference

based on heuristic

inferred from title

Agustín Tortajada

object named as

Agustín Tortajada

1

0 references

Margarita López-Trascasa

object named as

Margarita López-Trascasa

4

0 references

Santiago Rodriguez de Córdoba

object named as

Santiago Rodríguez de Córdoba

6

0 references

Pilar Sánchez-Corral

5

object named as

Pilar Sánchez-Corral

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

2

object named as

Sheila Pinto

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

author name string

Jorge Martínez-Ara

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

language of work or name

0 references

publication date

31 August 2011

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Kidney International

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

81

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

56-63

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Control of the amplification convertase of complement by the plasma protein beta1H

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Modulation of C3b hemolytic activity by a plasma protein distinct from C3b inactivator

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Human complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solution

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Regulation by membrane sialic acid of β1H-dependent decay-dissociation of amplification C3 convertase of the alternative complement pathway

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

The complete amino acid sequence of human complement factor H

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic and environmental factors influencing the human factor H plasma levels

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of three physically and functionally distinct binding sites for C3b in human complement factor H by deletion mutagenesis

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Discrimination between activators and nonactivators of the alternative pathway of complement: regulation via a sialic acid/polyanion binding site on factor H

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular mechanisms of target recognition in an innate immune system: interactions among factor H, C3b, and target in the alternative pathway of human complement

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional analysis in serum from atypical Hemolytic Uremic Syndrome patients reveals impaired protection of host cells associated with mutations in factor H.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

C3 glomerulopathy: a new classification

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement and diseases: defective alternative pathway control results in kidney and eye diseases

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

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.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement factor H polymorphism and age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement factor H variant increases the risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

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.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Measurement of factor H variants in plasma using variant-specific monoclonal antibodies: application to assessing risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural basis for engagement by complement factor H of C3b on a self surface

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

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.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

A new screening test for C3 nephritis factor based on a stable cell bound convertase on sheep erythrocytes

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

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.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2011.291

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/KI.2011.291

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33396948&oldid=2195321386"