Literature DB >> 1184014

C3 polymorphism in relation to age.

H Sorensen, J Dissing.   

Abstract

The C3 phenotype distribution was investigated in different age-groups among 2,078 voluntary blood donors between the ages of 20 and 65 years, in a group of unrelated babies and in a group of old healthy persons. A continuous increase in the C3F gene frequency with age was found among the blood donors varying from 0.1780 in the youngest age group (babies: 0.1585) to 0.2516 at the age of 50-55 years followed by a continuous decrease to a level of 0.1700 among the eldest donors (01718 among the old persons). In the age group 45-49 years the C3 distribution differed significantly from that in the adjoining age-groups (C3F = 0.1619). It is believed that the variations are brought about by selection of the blood donor population and a balanced polymorphism for the C3 system, possibly due to differences in the biological efficiency of the C3 variants in the complement sequence.

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Year:  1975        PMID: 1184014     DOI: 10.1159/000152737

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  2 in total

1.  C3 polymorphism, HLA and chronic renal failure in Spaniards.

Authors:  J R Regueiro; A Arnaiz-Villena
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

2.  Further studies of the down-regulation by Factor I of the C3b feedback cycle using endotoxin as a soluble activator and red cells as a source of CR1 on sera of different complotype.

Authors:  P J Lachmann; E Lay; D J Seilly; A Buchberger; W Schwaeble; J Khadake
Journal:  Clin Exp Immunol       Date:  2015-11-05       Impact factor: 4.330

  2 in total

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