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Journal Abstract Search

183 related items for PubMed ID: 6252944

  • 1. The fluidity gradient in erythrocyte membranes in hereditary spherocytosis: a spin label study.
    Jansson SE, Johnsson R, Gripenberg J, Vuopio P.
    Br J Haematol; 1980 Sep; 46(1):73-8. PubMed ID: 6252944
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  • 2. Membrane characteristics and metabolic properties of glucose-6-phosphate dehydrogenase deficient red cells.
    Jansson SE, Hekali R, Gripenberg J, Härkönen M, Vuopio P.
    Br J Haematol; 1980 Sep; 46(1):79-87. PubMed ID: 6252945
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  • 3. A spin-label study of membrane proteins and internal microviscosity of erythrocytes in hereditary spherocytosis.
    Bartosz G, Gaczyńska M, Grzelińska E, Judkiewicz L.
    Life Sci; 1987 Nov 16; 41(20):2285-8. PubMed ID: 2824948
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  • 4. Analysis of spin-labeled erythrocyte membranes.
    Fung LW.
    Ann N Y Acad Sci; 1983 Nov 16; 414():162-8. PubMed ID: 6322652
    [No Abstract] [Full Text] [Related]

  • 5. Detection of erythrocyte membrane protein alterations in hereditary spherocytosis through the use of thermal stress: a spin label study.
    Fung LW, Ostrowski MS, Meena WA, Sarnaik S.
    Life Sci; 1981 Nov 16; 29(20):2071-9. PubMed ID: 6273682
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  • 10. Biophysical studies of erythrocyte membranes from patients with duchenne muscular dystrophy.
    Dellantonio R, Angeleri F, Capriotti M, Lenaz G, Curatola G, Mazzanti L, Bertoli E.
    Ital J Biochem; 1980 Nov 16; 29(2):121-8. PubMed ID: 6250994
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  • 11. Saturation transfer EPR studies of membrane alteration in hereditary spherocytosis.
    Fung LW, Ostrowski MS.
    Life Sci; 1984 Nov 12; 35(20):2071-8. PubMed ID: 6092813
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  • 12. Phosphorylation in erythrocyte membranes from abnormally shaped cells.
    Greenquist AC, Shohet SB.
    Blood; 1976 Dec 12; 48(6):877-86. PubMed ID: 187264
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  • 13. Spin-label studies of erythrocytes in myotonic dystrophy: no increase in membrane fluidity.
    Gaffney BJ, Drachman DB, Lin DC, Tennekoon G.
    Neurology; 1980 Mar 12; 30(3):272-6. PubMed ID: 7189026
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  • 14. Erythrocyte cellular and membrane deformability in hereditary spherocytosis.
    Nakashima K, Beutler E.
    Blood; 1979 Mar 12; 53(3):481-5. PubMed ID: 760862
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  • 17. Organization of membrane lipids and proteins in human En(a-) erythrocytes that lack the major sialoglycoprotein, glycophorin A. A spin-label study.
    Jansson SE, Gripenberg J, Hekali R, Gahmberg CG.
    Biochem J; 1981 Apr 01; 195(1):123-8. PubMed ID: 6272742
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  • 20. Normal fluidity of red cell membranes in hereditary spherocytosis.
    Cooper RA, Sawyer WH, Leslie MH, Hill JS, Gill FM, Wiley JS.
    Br J Haematol; 1980 Oct 01; 46(2):299-301. PubMed ID: 7426455
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