Literature DB >> 14224515

SERUM ALBUMIN: POLYMORPHISM IN MAN.

G EFREMOV, M BRAEND.   

Abstract

Serums from 1015 individuals, mainly Norwegians, were studied by starch-gel electrophoresis. All but one showed the same albumin phenotype. The appearance of the exceptional sample on starch gel fits with that of a heterozygote. A genetic theory of two alleles Al(F) and Al(S) is proposed.

Entities:  

Keywords:  BLOOD PROTEIN ELECTROPHORESIS; GENETICS, HUMAN; NORWAY; PREGNANCY; SERUM ALBUMIN

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Substances:

Year:  1964        PMID: 14224515     DOI: 10.1126/science.146.3652.1679

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  4 in total

1.  Acquired bisalbuminemia with hyperamylasemia.

Authors:  G G Shashaty; M A Atamer
Journal:  Am J Dig Dis       Date:  1972-01

2.  [A human serum albumin variant (bisalbuminaemia). Occurrence and heredity in a family (area of Berlin)].

Authors:  M Rose; J Blaszczyk; G Geserick
Journal:  Humangenetik       Date:  1971

3.  [Alloalbuminemia (double albuminemia)].

Authors:  A Fateh-Moghadam; J Eisenburg; R Lamerz
Journal:  Klin Wochenschr       Date:  1969-09-15

4.  Genetic diversity in serum albumin.

Authors:  M S Adams
Journal:  J Med Genet       Date:  1966-09       Impact factor: 6.318

  4 in total

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