These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
115 related articles for article (PubMed ID: 2211672)
1. Entrapment of purified alpha-hemoglobin chains in normal erythrocytes. A model for beta thalassemia. Scott MD; Rouyer-Fessard P; Lubin BH; Beuzard Y J Biol Chem; 1990 Oct; 265(29):17953-9. PubMed ID: 2211672 [TBL] [Abstract][Full Text] [Related]
2. Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytes. Scott MD; van den Berg JJ; Repka T; Rouyer-Fessard P; Hebbel RP; Beuzard Y; Lubin BH J Clin Invest; 1993 Apr; 91(4):1706-12. PubMed ID: 7682576 [TBL] [Abstract][Full Text] [Related]
3. Entrapment of purified alpha-hemoglobin chains in normal erythrocytes as a model for human beta thalassemia. Scott MD Adv Exp Med Biol; 1992; 326():139-48. PubMed ID: 1295299 [TBL] [Abstract][Full Text] [Related]
4. Fate of alpha-hemoglobin chains and erythrocyte defects in beta-thalassemia. Rouyer-Fessard P; Scott MD; Leroy-Viard K; Garel MC; Bachir D; Galacteros F; Beuzard Y Ann N Y Acad Sci; 1990; 612():106-17. PubMed ID: 2291540 [TBL] [Abstract][Full Text] [Related]
5. Mouse beta thalassemia, a model for the membrane defects of erythrocytes in the human disease. Rouyer-Fessard P; Leroy-Viard K; Domenget C; Mrad A; Beuzard Y J Biol Chem; 1990 Nov; 265(33):20247-51. PubMed ID: 2243088 [TBL] [Abstract][Full Text] [Related]
6. Alpha- and beta-haemoglobin chain induced changes in normal erythrocyte deformability: comparison to beta thalassaemia intermedia and Hb H disease. Scott MD; Rouyer-Fessard P; Ba MS; Lubin BH; Beuzard Y Br J Haematol; 1992 Apr; 80(4):519-26. PubMed ID: 1581237 [TBL] [Abstract][Full Text] [Related]
7. Cellular and membrane properties of alpha and beta thalassemic erythrocytes are different: implication for differences in clinical manifestations. Schrier SL; Rachmilewitz E; Mohandas N Blood; 1989 Nov; 74(6):2194-202. PubMed ID: 2804358 [TBL] [Abstract][Full Text] [Related]
8. A study of membrane protein defects and alpha hemoglobin chains of red blood cells in human beta thalassemia. Rouyer-Fessard P; Garel MC; Domenget C; Guetarni D; Bachir D; Colonna P; Beuzard Y J Biol Chem; 1989 Nov; 264(32):19092-8. PubMed ID: 2808414 [TBL] [Abstract][Full Text] [Related]
9. Oxidative denaturation of red blood cells in thalassemia. Shinar E; Rachmilewitz EA Semin Hematol; 1990 Jan; 27(1):70-82. PubMed ID: 2405497 [TBL] [Abstract][Full Text] [Related]
10. Differential regulation of redox proteins and chaperones in HbEβ-thalassemia erythrocyte proteome. Bhattacharya D; Saha S; Basu S; Chakravarty S; Chakravarty A; Banerjee D; Chakrabarti A Proteomics Clin Appl; 2010 May; 4(5):480-8. PubMed ID: 21137065 [TBL] [Abstract][Full Text] [Related]
11. The role of membrane protein sulfhydryl groups in hydrogen peroxide-mediated membrane damage in human erythrocytes. Snyder LM; Fortier NL; Leb L; McKenney J; Trainor J; Sheerin H; Mohandas N Biochim Biophys Acta; 1988 Jan; 937(2):229-40. PubMed ID: 3337802 [TBL] [Abstract][Full Text] [Related]
12. Oxidative red blood cell membrane injury in the pathophysiology of severe mouse beta-thalassemia. Advani R; Rubin E; Mohandas N; Schrier SL Blood; 1992 Feb; 79(4):1064-7. PubMed ID: 1737090 [TBL] [Abstract][Full Text] [Related]
13. Turnover of excess hemoglobin alpha chains in beta-thalassemic cells is ATP-dependent. Shaeffer JR J Biol Chem; 1983 Nov; 258(21):13172-7. PubMed ID: 6195159 [TBL] [Abstract][Full Text] [Related]
14. Characterization and comparison of the red blood cell membrane damage in severe human alpha- and beta-thalassemia. Advani R; Sorenson S; Shinar E; Lande W; Rachmilewitz E; Schrier SL Blood; 1992 Feb; 79(4):1058-63. PubMed ID: 1737089 [TBL] [Abstract][Full Text] [Related]
15. Alterations of red cell membrane proteins and hemoglobin under natural and experimental oxidant stress. Alloisio N; Michelon D; Bannier E; Revol A; Beuzard Y; Delaunay J Biochim Biophys Acta; 1982 Oct; 691(2):300-8. PubMed ID: 7138863 [No Abstract] [Full Text] [Related]
16. Phospholipid composition and organization in model beta-thalassemic erythrocytes. Kuypers FA; Schott MA; Scott MD Am J Hematol; 1996 Jan; 51(1):45-54. PubMed ID: 8571937 [TBL] [Abstract][Full Text] [Related]
17. Differences in affinity of beta and delta hemoglobin chains for alpha chains. A possible explanation for the variation in the percentages of hemoglobin A2 in thalassemia and other disorders. Martínez G; Menéndez R Biochim Biophys Acta; 1983 Mar; 743(2):256-9. PubMed ID: 6824703 [TBL] [Abstract][Full Text] [Related]
18. ATP-dependent proteolysis of hemoglobin alpha chains in beta-thalassemic hemolysates is ubiquitin-dependent. Shaeffer JR J Biol Chem; 1988 Sep; 263(27):13663-9. PubMed ID: 2843527 [TBL] [Abstract][Full Text] [Related]
19. Association of hemoglobin chains with the cell membrane as a cause of red cell distortion in thalassemia. Kirschner-Zilber I; Setter E; Shaklai N Biochem Med Metab Biol; 1987 Aug; 38(1):19-31. PubMed ID: 3663395 [TBL] [Abstract][Full Text] [Related]
20. [Methemoglobin level and its comparison with levels of globins and membrane proteins in erythrocytes of patients with beta-thalassemia]. Iagubova VI; Alekperova GA; Askerova TA; Dadashova TS Klin Lab Diagn; 2004 May; (5):47-50. PubMed ID: 15230119 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]