Polymorphism of human haptoglobin and its clinical importance: [review]
Genet. mol. biol
; Genet. mol. biol;31(3): 602-620, 2008. ilus, tab
Article
в En
| LILACS
| ID: lil-490044
Ответственная библиотека:
BR1.1
ABSTRACT
Haptoglobin (Hp) is a plasma glycoprotein, the main biological function of which is to bind free hemoglobin (Hb) and prevent the loss of iron and subsequent kidney damage following intravascular hemolysis. Haptoglobin is also a positive acute-phase protein with immunomodulatory properties. In humans, the HP locus is polymorphic, with two codominant alleles (HP1 and HP2) that yield three distinct genotypes/phenotypes (Hp1-1, Hp2-1 and Hp2-2). The corresponding proteins have structural and functional differences that may influence the susceptibility and/or outcome in several diseases. This article summarizes the available data on the structure and functions of Hp and the possible effects of Hp polymorphism in a number of important human disorders.
Полный текст:
1
База данных:
LILACS
Язык:
En
Журнал:
Genet. mol. biol
/
Genet. mol. biol. (Online)
/
Genetics and molecular biology (Impresso)
Тематика журнала:
GENETICA
Год:
2008
Тип:
Article
/
Project document