Complement factor H and the hemolytic uremic syndrome (Q24676234)

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Language	Label	Description	Also known as
English	Complement factor H and the hemolytic uremic syndrome	scientific article

Statements

instance of

scholarly article

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review article

1 reference

stated in

PubMed

retrieved

31 December 2023

title

Complement factor H and the hemolytic uremic syndrome (English)

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main subject

hemolytic-uremic syndrome

1 reference

stated in

PubMed

retrieved

29 May 2020

macular degeneration

1 reference

stated in

PubMed

retrieved

19 September 2019

immunological model

1 reference

stated in

PubMed

retrieved

19 September 2019

animal disease model

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stated in

PubMed

retrieved

3 December 2020

complement activation, alternative pathway

1 reference

PubMed publication ID

17548524

author

Timothy H J Goodship

series ordinal

2

object named as

Timothy H J Goodship

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John P Atkinson

series ordinal

1

object named as

John P Atkinson

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language of work or name

English

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publication date

11 June 2007

6 references

stated in

PubMed Central

retrieved

25 April 2019

stated in

PubMed Central

retrieved

20 June 2019

stated in

PubMed Central

retrieved

19 September 2019

stated in

PubMed Central

retrieved

29 May 2020

stated in

PubMed Central

retrieved

3 December 2020

stated in

PubMed Central

retrieved

31 December 2023

published in

Journal of Experimental Medicine

5 references

stated in

PubMed Central

retrieved

25 April 2019

stated in

PubMed Central

retrieved

20 June 2019

stated in

PubMed Central

retrieved

19 September 2019

stated in

PubMed Central

retrieved

3 December 2020

stated in

PubMed Central

retrieved

31 December 2023

volume

204

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issue

6

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page(s)

1245-8

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cites work

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

7 April 2017

Complement factor H polymorphism in age-related macular degeneration

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

7 April 2017

Complement factor H polymorphism and age-related macular degeneration

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

Atypical haemolytic uraemic syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

Genetic studies into inherited and sporadic hemolytic uremic syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

Familial hypocomplementemic hemolytic uremic syndrome with HLA-A3,B7 haplotype

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 September 2017

Membrane cofactor protein (CD46) protects cells from complement-mediated attack by an intrinsic mechanism

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

30 May 2018

Escherichia coli O157:H7

2 references

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1084%2FJEM.20070664

retrieved

21 January 2018

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17548524

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2118604

retrieved

28 November 2018

Hypocomplementaemia due to a genetic deficiency of beta 1H globulin

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17548524

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1084/JEM.20070664

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PMC publication ID

2118604

0 references

PubMed publication ID

17548524

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ResearchGate publication ID

6287151

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