(Q33852651)

29 July 2017

1 reference

title

Properdin deficiency: molecular basis and disease association (English)

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29 July 2017

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Fijen CA

1

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29 July 2017

van den Bogaard R

2

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29 July 2017

Schipper M

3

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29 July 2017

Mannens M

4

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29 July 2017

Schlesinger M

5

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29 July 2017

Nordin FG

6

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29 July 2017

Dankert J

7

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29 July 2017

Daha MR

8

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29 July 2017

Sjöholm AG

9

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29 July 2017

Truedsson L

10

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29 July 2017

Kuijper EJ

11

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29 July 2017

language of work or name

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1 September 1999

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29 July 2017

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29 July 2017

volume

36

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29 July 2017

issue

13-14

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29 July 2017

page(s)

863-867

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Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

The excessive complement activation in fulminant meningococcal septicemia is predominantly caused by alternative pathway activation

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Genetic and physical mapping around the properdin P gene

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Recurrent meningococcal septicaemia and properdin deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Properdin: binding to C3b and stabilization of the C3b-dependent C3 convertase

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Infectious diseases associated with complement deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Carrier detection by microsatellite haplotyping in 10 properdin type 1-deficient families

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Assessment of complement deficiency in patients with meningococcal disease in The Netherlands

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Properdin, the terminal complement components, thrombospondin and the circumsporozoite protein of malaria parasites contain similar sequence motifs

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Recognition and control of neisserial infection by antibody and complement.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Complement deficiencies in selected groups of patients with meningococcal disease

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Complement and immunoglobulin studies in 15 cases of chronic meningococcemia: properdin deficiency and hypoimmunoglobulinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Complete primary structure of human properdin: a positive regulator of the alternative pathway of the serum complement system

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Characterization of the human properdin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Expression of properdin in complete and incomplete deficiency: normal in vitro synthesis by monocytes in two cases with properdin deficiency type II due to distinct mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

The properdin system and immunity. I. Demonstration and isolation of a new serum protein, properdin, and its role in immune phenomena

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Hereditary properdin deficiency in three families of Tunisian Jews

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

A second variant of properdin deficiency: the detection of properdin at low concentrations in affected males.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Dysfunctional properdin in a Dutch family with meningococcal disease

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Human properdin deficiency has a heterogeneous genetic background

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

Covalent linkage of C3 to properdin during complement activation

1 reference

https://api.crossref.org/works/10.1016%2FS0161-5890%2899%2900107-8

7 January 2021

10.1016/S0161-5890(99)00107-8

Identifiers

DOI

1 reference

29 July 2017

1 reference