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Items: 1 to 20 of 355

1.

Theoretical model of thalassemic erythrocyte shape transformation.

Pawlowski PH, Burzyńska B, Zielenkiewicz P.

J Theor Biol. 2008 Oct 7;254(3):575-9. doi: 10.1016/j.jtbi.2008.06.029. Epub 2008 Jul 3.

PMID:
18652835
2.

Theoretical model of reticulocyte to erythrocyte shape transformation.

Pawlowski PH, Burzyńska B, Zielenkiewicz P.

J Theor Biol. 2006 Nov 7;243(1):24-38. Epub 2006 Jun 20.

PMID:
16876199
4.

Alterations and pathology of thalassemic red cells: comparison between alpha- and beta-thalassemia.

Bunyaratvej A, Fucharoen S, Butthep P, Sae-ung N, Kamchonwongpaisan S, Khuhapinant A.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:257-60.

PMID:
8629118
5.

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 15;265(29):17953-9.

6.

Cell membrane and volume changes during red cell development and aging.

Mohandas N, Groner W.

Ann N Y Acad Sci. 1989;554:217-24. Review.

PMID:
2660673
7.

Six-day stability of erythrocyte and reticulocyte parameters in-vitro: a comparison of blood samples from healthy, iron-deficient, and thalassemic individuals.

Sudmann-Day ÅA, Piehler A, Klingenberg O, Urdal P.

Scand J Clin Lab Invest. 2015 May;75(3):247-53. doi: 10.3109/00365513.2014.1000370. Epub 2015 Jan 22.

PMID:
25608597
8.
9.
10.

Inhibition by beta-thalassemic erythrocytes of erythropoiesis in vitro.

Vedovato M, Salvatorelli G.

Cytobios. 1989;58(232):35-7.

PMID:
2791648
11.

Why does the thalassemic red cell die?

Schrier SL.

Blood Cells. 1986;12(1):91-8. No abstract available.

PMID:
3790740
12.

Osmotic swelling and hole formation in membranes of thalassemic and spherocytic erythrocytes.

Pribush A, Hatskelzon L, Kapelushnik J, Meyerstein N.

Blood Cells Mol Dis. 2003 Jul-Aug;31(1):43-7.

PMID:
12850482
13.

Membrane assembly and remodeling during reticulocyte maturation.

Chasis JA, Prenant M, Leung A, Mohandas N.

Blood. 1989 Aug 15;74(3):1112-20.

14.

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. Review.

PMID:
2291540
15.

Influence of hyperglycemia on aggregation, deformability and shape parameters of erythrocytes.

Babu N, Singh M.

Clin Hemorheol Microcirc. 2004;31(4):273-80.

PMID:
15567897
16.

Spectroscopical and mechanical characterization of normal and thalassemic red blood cells by Raman Tweezers.

De Luca AC, Rusciano G, Ciancia R, Martinelli V, Pesce G, Rotoli B, Selvaggi L, Sasso A.

Opt Express. 2008 May 26;16(11):7943-57.

PMID:
18545504
17.

Topological features of erythrocytes in thalassemic patients: quantitative characterization by scanning electron and atomic force microscopy.

Mukherjee R, Chaudhury K, Chakraborty C.

Anal Quant Cytopathol Histpathol. 2014 Apr;36(2):91-9.

PMID:
24902361
18.

Member-associated changes during erythropoiesis. On the mechanism of maturation of reticulocytes to erythrocytes.

Zweig SE, Tokuyasu KT, Singer SJ.

J Supramol Struct Cell Biochem. 1981;17(2):163-81.

PMID:
7321058
19.
20.

Biophysical characterization of beta-thalassemic red blood cells.

Desouky OS, Selim NS, El-Bakrawy EM, El-Marakby SM.

Cell Biochem Biophys. 2009;55(1):45-53. doi: 10.1007/s12013-009-9056-5. Epub 2009 Jul 8.

PMID:
19585085

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