(Q33395944)

26 July 2017

title

Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP. (English)

1 reference

atypical hemolytic uremic syndrome

26 July 2017

main subject

1 reference

Michal Malina

3

0 references

Iuri Marinov

object named as

Iuri Marinov

5

0 references

Ingrid Hrachovinová

7

object named as

Ingrid Hrachovinova

1 reference

26 July 2017

Dana Provaznikova

1

1 reference

26 July 2017

Simon Rittich

2

1 reference

26 July 2017

Tomas Seeman

4

1 reference

26 July 2017

Magdalena Riedl

6

1 reference

26 July 2017

publication date

27 June 2011

1 reference

26 July 2017

1 reference

26 July 2017

volume

27

1 reference

26 July 2017

issue

1

1 reference

26 July 2017

page(s)

73-81

1 reference

https://scigraph.springernature.com/pub.10.1007/s00467-011-1943-5

26 July 2017

exact match

0 references

cites work

Thrombotic Microangiopathies

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Escherichia coliO157:H7 and the Hemolytic–Uremic Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Hemolytic Uremic Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Atypical (non-diarrhea-associated) hemolytic-uremic syndrome in childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Functional properties of complement factor H-related proteins FHR-3 and FHR-4: binding to the C3d region of C3b and differential regulation by heparin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Familial haemolytic uraemic syndrome and an MCP mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Thrombomodulin mutations in atypical hemolytic-uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Membrane cofactor protein (MCP; CD46): isoform-specific tyrosine phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

MutationTaster evaluates disease-causing potential of sequence alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Hemolytic uremic syndrome recurrence after renal transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Dissecting Sites Important for Complement Regulatory Activity in Membrane Cofactor Protein (MCP; CD46)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1943-5

Genetic studies into inherited and sporadic hemolytic uremic syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21706448

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Purification of human genomic DNA from whole blood using sodium perchlorate in place of phenol

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21706448

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00467-011-1943-5

1 reference

Dimensions Publication ID

26 July 2017

1043907022

0 references

1 reference