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Complement factor H and the haemolytic uraemic syndrome
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
title
Complement factor H and the haemolytic uraemic syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
author name string
C M Taylor
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
language of work or name
English
0 references
publication date
1 October 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
volume
358
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
issue
9289
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
page(s)
1200-1202
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
cites work
Factor H and the pathogenesis of renal diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hemolytic-uremic syndrome and complement factor H deficiency: clinical aspects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complement factor H: physiology and pathophysiology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Folded-back solution structure of monomeric factor H of human complement by synchrotron X-ray and neutron scattering, analytical ultracentrifugation and constrained molecular modelling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
C-Reactive protein binds to apoptotic cells, protects the cells from assembly of the terminal complement components, and sustains an antiinflammatory innate immune response: implications for systemic autoimmunity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemolytic uremic syndrome associated with complement factor H deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2906339-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(01)06339-5
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
PubMed ID
11675053
1 reference
stated in
Europe PubMed Central
PubMed ID
11675053
retrieved
25 July 2017
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