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Journal Abstract Search


185 related items for PubMed ID: 11222393

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  • 3. Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease.
    Shmukler BE, Rivera A, Bhargava P, Nishimura K, Hsu A, Kim EH, Trudel M, Rust MB, Hubner CA, Brugnara C, Alper SL.
    Blood Cells Mol Dis; 2019 Nov; 79():102346. PubMed ID: 31352162
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  • 4. Treatment with oral clotrimazole blocks Ca(2+)-activated K+ transport and reverses erythrocyte dehydration in transgenic SAD mice. A model for therapy of sickle cell disease.
    De Franceschi L, Saadane N, Trudel M, Alper SL, Brugnara C, Beuzard Y.
    J Clin Invest; 1994 Apr; 93(4):1670-6. PubMed ID: 7512989
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  • 6. Volume control in sickle cells is facilitated by the novel anion conductance inhibitor NS1652.
    Bennekou P, Pedersen O, Møller A, Christophersen P.
    Blood; 2000 Mar 01; 95(5):1842-8. PubMed ID: 10688846
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  • 9. Sickle cell disease: from membrane pathophysiology to novel therapies for prevention of erythrocyte dehydration.
    Brugnara C.
    J Pediatr Hematol Oncol; 2003 Dec 01; 25(12):927-33. PubMed ID: 14663274
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  • 10. Red blood cells of a transgenic mouse expressing high levels of human hemoglobin S exhibit deoxy-stimulated cation flux.
    Romero JR, Fabry ME, Suzuka S, Nagel RL, Canessa M.
    J Membr Biol; 1997 Oct 01; 159(3):187-96. PubMed ID: 9312208
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  • 11. Erythrocyte dehydration in pathophysiology and treatment of sickle cell disease.
    Brugnara C.
    Curr Opin Hematol; 1995 Mar 01; 2(2):132-8. PubMed ID: 9371983
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  • 12. Inhibition of the endogenous volume-regulated anion channel (VRAC) in HEK293 cells by acidic di-aryl-ureas.
    Hélix N, Strøbaek D, Dahl BH, Christophersen P.
    J Membr Biol; 2003 Nov 15; 196(2):83-94. PubMed ID: 14724745
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  • 13. Age decline in the activity of the Ca2+-sensitive K+ channel of human red blood cells.
    Tiffert T, Daw N, Etzion Z, Bookchin RM, Lew VL.
    J Gen Physiol; 2007 May 15; 129(5):429-36. PubMed ID: 17470662
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  • 14. Comparison of the effects of radiographic contrast media on dehydration and filterability of red blood cells from donors homozygous for hemoglobin A or hemoglobin S.
    Losco P, Nash G, Stone P, Ventre J.
    Am J Hematol; 2001 Nov 15; 68(3):149-58. PubMed ID: 11754395
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  • 15. Dipyridamole inhibits sickling-induced cation fluxes in sickle red blood cells.
    Joiner CH, Jiang M, Claussen WJ, Roszell NJ, Yasin Z, Franco RS.
    Blood; 2001 Jun 15; 97(12):3976-83. PubMed ID: 11389043
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  • 16. Quercetin Completely Ameliorates Hypoxia-Reoxygenation-Induced Pathophysiology Severity in NY1DD Transgenic Sickle Mice: Intrinsic Mild Steady State Pathophysiology of the Disease in NY1DD Is Also Reversed.
    Thangaswamy S, Branch CA, Ambadipudi K, Acharya SA.
    Biomolecules; 2021 Oct 06; 11(10):. PubMed ID: 34680105
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  • 17. Therapeutic strategies for prevention of sickle cell dehydration.
    Brugnara C.
    Blood Cells Mol Dis; 2001 Oct 06; 27(1):71-80. PubMed ID: 11358364
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  • 18. Formation of dense erythrocytes in SAD mice exposed to chronic hypoxia: evaluation of different therapeutic regimens and of a combination of oral clotrimazole and magnesium therapies.
    De Franceschi L, Brugnara C, Rouyer-Fessard P, Jouault H, Beuzard Y.
    Blood; 1999 Dec 15; 94(12):4307-13. PubMed ID: 10590075
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  • 19. Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia.
    Orringer EP, Blythe DS, Johnson AE, Phillips G, Dover GJ, Parker JC.
    Blood; 1991 Jul 01; 78(1):212-6. PubMed ID: 1712641
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  • 20. Two distinct pathways mediate the formation of intermediate density cells and hyperdense cells from normal density sickle red blood cells.
    Schwartz RS, Musto S, Fabry ME, Nagel RL.
    Blood; 1998 Dec 15; 92(12):4844-55. PubMed ID: 9845552
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