Platelet proteomics in thalassemia: Factors responsible for hypercoagulation

Author:

Karmakar Shilpita1,Banerjee Debasis23,Chakrabarti Abhijit4

Affiliation:

1. Biophysics and Structural Genomics Division; Saha Institute of Nuclear Physics; Kolkata India

2. Hematology Unit; Ramakrishna Mission Seva Prathisthan; Kolkata India

3. Clinical Haematology Service; Park Clinic; Kolkata India

4. Crystallography and Molecular Biology Division; Saha Institute of Nuclear Physics; Kolkata India

Publisher

Wiley

Subject

Clinical Biochemistry

Reference37 articles.

1. Differential regulation of redox proteins and chaperones in HbEβ-thalassemia erythrocyte proteome;Bhattacharya;Proteomics Clin. Appl.,2010

2. Loss of phospholipid membrane asymmetry and sialylated glycoconjugates from erythrocyte surface in haemoglobin Eβ-thalassaemia;Basu;Br. J. Haematol.,2008

3. Characterizations and proteome analysis of platelet-free plasma-derived microparticles in β-thalassemia/hemoglobin E patients;Chaichompoo;J. Proteomics,2012

4. Medical progress β-thalassemia;Rund;N. Engl. J. Med.,2005

5. Coagulopathy in beta thalassemia: current understanding and future perspectives;Cappellini;Medit. J. Hemat. Infect Dis.,2009

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