Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis-Reference-Cited by-同舟云学术

Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis

Published:2012-08 Issue:7-8 Volume:6 Page:403-411
ISSN:1862-8346
Container-title:PROTEOMICS - Clinical Applications
language:en
Short-container-title:Prot. Clin. Appl.

Author:

Demiralp Duygu Ozel¹,Peker Selen¹,Turgut Burhan²,Akar Nejat³

Affiliation:

1. Ankara University Biotechnology Institute; Ankara Turkey

2. Department; of Child Health and Diseases; TOBB University; Ankara Turkey

3. Department of Hematology, Medical School; Namik Kemal University; Tekirdag Turkey

Funder

Scientific and Technological Research Council of Turkey

Publisher

Wiley

Subject

Clinical Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/prca.201200010/fullpdf

Reference51 articles.

1. Disorders of red cell membrane;An;Br. J. Haematol.,2008

2. Clinical expression and laboratory detection of red blood cell membrane protein mutations;Palek;Semin. Hematol.,1993

3. Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis;Coetzer;Blood,1987

4. Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin;Glele-Kakai;Br. J. Haematol.,1996

5. Red-cell cytoskeletal abnormalities-implications for malaria;Nagel;N. Engl. J. Med.,1990

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