(Q28303343)

Maria A Miteva

4

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Leendert A Trouw

Leendert A Trouw

2

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Bruno O Villoutreix

Bruno O Villoutreix

11

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Anna M. Blom

Anna M Blom

12

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Klaus Müller

8

Klaus Muller

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H V Marquart

Hanne Marquart

7

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Ferah Genel

5

Ferah Genel

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author name string

Sara C Nilsson

1

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Marta Zelazko

6

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Anders G Sjöholm

9

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Lennart Truedsson

European Journal of Immunology

10

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language of work or name

English

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publication date

January 2009

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published in

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volume

39

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issue

1

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page(s)

310-23

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cites work

Complement factor I deficiency associated with recurrent meningitis coinciding with menstruation

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Recurrent infections in partial complement factor I deficiency: evaluation of three generations of a Brazilian family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Complement factor I deficiency in a family with recurrent infections

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

The molecular basis of hereditary complement factor I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Molecular characterization of homozygous hereditary factor I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Deficiency of human complement factor I associated with lowered factor H.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

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/10.1002%2FEJI.200838702

Atypical haemolytic uraemic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Characterization of primary amino acid sequence of human complement control protein factor I from an analysis of cDNA clones

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Complement biosynthesis by the human hepatoma-derived cell line HepG2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Modulation of the classical pathway C3 convertase by plasma proteins C4 binding protein and C3b inactivator

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

The organization of the human complement factor I gene (IF): a member of the serine protease gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Possible arrangement of the five domains in human complement factor I as determined by a combination of X-ray and neutron scattering and homology modeling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

The catalytically active serine protease domain of human complement factor I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Molecular structures from low angle X-ray and neutron scattering studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Processing of human factor I in COS-1 cells co-transfected with factor I and paired basic amino acid cleaving enzyme (PACE) cDNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Purification of human C4b-binding protein and formation of its complex with vitamin K-dependent protein S

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

CCP1-4 of the C4b-binding protein alpha-chain are required for factor I mediated cleavage of complement factor C3b.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Evaluating conformational free energies: the colony energy and its application to the problem of loop prediction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Crystal structure of a scavenger receptor cysteine-rich domain sheds light on an ancient superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Molecular basis of familial hypercholesterolaemia from structure of LDL receptor module

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

The crystal structure of the catalytic domain of human urokinase-type plasminogen activator

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

The factor VII zymogen structure reveals reregistration of beta strands during activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

Glomerulonephritis in a patient with complement factor I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

7 January 2021

Inherited complete factor I deficiency associated with systemic lupus erythematosus, higher susceptibility to infection and low levels of factor H

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

7 January 2021

Molecular characterization of Complement Factor I deficiency in two Spanish families

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

7 January 2021

Mapping of the human complement factor I gene to 4q25

1 reference

https://api.crossref.org/works/10.1002%2FEJI.200838702

7 January 2021