Literature DB >> 8340678

Genetics and deficiencies of the soluble regulatory proteins of the complement system.

R B Sim1, K Kölble, M A McAleer, O Dominguez, V M Dee.   

Abstract

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Year:  1993        PMID： 8340678     DOI： 10.3109/08830189309051172

Source DB:  PubMed          Journal:  Int Rev Immunol        ISSN： 0883-0185            Impact factor:   5.311


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  11 in total

Review 1.  Complement deficiency.

Authors:  K M O'Neil
Journal:  Clin Rev Allergy Immunol       Date:  2000-10       Impact factor: 8.667

2.  Different regulation of factor H and FHL-1/reconectin by inflammatory mediators and expression of the two proteins in rheumatoid arthritis (RA).

Authors:  M A Friese; J Hellwage; T S Jokiranta; S Meri; H J Müller-Quernheim; H H Peter; H Eibel; P F Zipfel
Journal:  Clin Exp Immunol       Date:  2000-08       Impact factor: 4.330

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

Authors:  A S Grumach; M F Leitão; V G Arruk; M Kirschfink; A Condino-Neto
Journal:  Clin Exp Immunol       Date:  2006-02       Impact factor: 4.330

4.  Mapping the bovine factor H gene to chromosome 16 by SSCP analysis.

Authors:  J L Williams; D H Lester; V M Teres; W Barendse; R B Sim; C J Soames
Journal:  Mamm Genome       Date:  1997-01       Impact factor: 2.957

5.  Identification of human complement factor H as a chemotactic protein for monocytes.

Authors:  K Nabil; B Rihn; M C Jaurand; J M Vignaud; J Ripoche; Y Martinet; N Martinet
Journal:  Biochem J       Date:  1997-09-01       Impact factor: 3.857

6.  The human complement regulatory factor-H-like protein 1, which represents a truncated form of factor H, displays cell-attachment activity.

Authors:  J Hellwage; S Kühn; P F Zipfel
Journal:  Biochem J       Date:  1997-09-01       Impact factor: 3.857

7.  Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.

Authors:  L Ying; Y Katz; M Schlesinger; R Carmi; H Shalev; N Haider; G Beck; V C Sheffield; D Landau
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

8.  The role of Fcgamma receptor polymorphisms and C3 in the immune defence against Neisseria meningitidis in complement-deficient individuals.

Authors:  C A Fijen; R G Bredius; E J Kuijper; T A Out; M De Haas; A P De Wit; M R Daha; J G De Winkel
Journal:  Clin Exp Immunol       Date:  2000-05       Impact factor: 4.330

9.  The human factor H-related gene 2 (FHR2): structure and linkage to the coagulation factor XIIIb gene.

Authors:  C Skerka; J M Moulds; P Taillon-Miller; D Hourcade; P F Zipfel
Journal:  Immunogenetics       Date:  1995       Impact factor: 2.846

10.  Human Properdin Opsonizes Nanoparticles and Triggers a Potent Pro-inflammatory Response by Macrophages without Involving Complement Activation.

Authors:  Lubna Kouser; Basudev Paudyal; Anuvinder Kaur; Gudrun Stenbeck; Lucy A Jones; Suhair M Abozaid; Cordula M Stover; Emmanuel Flahaut; Robert B Sim; Uday Kishore
Journal:  Front Immunol       Date:  2018-02-12       Impact factor: 7.561
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