Oxidative stress in β-thalassemia: hemoglobin α-chains activate peroxidation of low density lipoproteins-Reference-Cited by-同舟云学术

Oxidative stress in β-thalassemia: hemoglobin α-chains activate peroxidation of low density lipoproteins

Published:1998 Issue:1-2 Volume:8 Page:169-172
ISSN:0951-6433
Container-title:BioFactors
language:en
Short-container-title:BioFactors

Author:

Altamentova Svetlana M.,Shaklai Nurith

Publisher

Wiley

Subject

Clinical Biochemistry,Molecular Medicine,General Medicine,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/biof.5520080129/fullpdf

Reference7 articles.

1. Formation of superoxide in the autoxidation of the isolated - and -chains of human hemoglobin and its involvement in hemichrome precipitation;Brunori;Eur. J. Biochem.,1975

2. Evidence for a concerted reaction between lipid hydroperoxides and polypeptides;Fruebis;Proc. Natl. Acad. Sci. USA,1992

3. Increased sensitivity of isolated alpha subunits of normal human hemoglobin to oxidative damage and crosslinkage with spectrin;Joshi;J. Lab. Clin. Med.,1983

4. Association of hemoglobin chains with the cell membrane as a cause of red cell distortion in thalassemia;Kirschner-Zilber;Biochem. Med. Metabol. Biol.,1987

5. Hemoglobin-induced apolipoprotein B crosslinking in low density lipoprotein peroxidation;Miller;Arch. Biochem. Biophys.,1996

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4. Superoxide and Nitric Oxide in Pathological Conditions Associated with Iron Overload. The Effects of Antioxidants and Chelators;Current Medicinal Chemistry;2005-11-01

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