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.
164 related articles for article (PubMed ID: 2917191)
41. Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain. Garbarz M; Lecomte MC; Féo C; Devaux I; Picat C; Lefebvre C; Galibert F; Gautero H; Bournier O; Galand C Blood; 1990 Apr; 75(8):1691-8. PubMed ID: 2328319 [TBL] [Abstract][Full Text] [Related]
42. Modeling of band-3 protein diffusion in the normal and defective red blood cell membrane. Li H; Zhang Y; Ha V; Lykotrafitis G Soft Matter; 2016 Apr; 12(15):3643-53. PubMed ID: 26977476 [TBL] [Abstract][Full Text] [Related]
43. Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide. Floyd PB; Gallagher PG; Valentino LA; Davis M; Marchesi SL; Forget BG Blood; 1991 Sep; 78(5):1364-72. PubMed ID: 1878597 [TBL] [Abstract][Full Text] [Related]
44. Canine elliptocytosis due to a mutant beta-spectrin. Di Terlizzi R; Gallagher PG; Mohandas N; Steiner LA; Dolce KS; Guo X; Wilkerson MJ; Stockham SL Vet Clin Pathol; 2009 Mar; 38(1):52-8. PubMed ID: 19228356 [TBL] [Abstract][Full Text] [Related]
45. [Family of hereditary elliptocytosis with abnormalities of spectrin function (Sp alpha 1/74)]. Okino E; Mori C; Yamazaki S; Toyota K; Yamada T; Tachi K; Shike S; Kanzaki A; Ikeda A; Yawata Y Rinsho Ketsueki; 1989 Jul; 30(7):1047-51. PubMed ID: 2810789 [TBL] [Abstract][Full Text] [Related]
46. Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis. Lecomte MC; Dhermy D; Garbarz M; Feo C; Gautero H; Bournier O; Picat C; Chaveroche I; Ester A; Galand C Hum Genet; 1985; 71(4):351-7. PubMed ID: 4077050 [TBL] [Abstract][Full Text] [Related]
47. Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability. Tchernia G; Mohandas N; Shohet SB J Clin Invest; 1981 Aug; 68(2):454-60. PubMed ID: 6894932 [TBL] [Abstract][Full Text] [Related]
48. [Clinical and biochemical study of 9 patients with hereditary elliptocytosis]. Feldman L; Marick T; Cerone S; Sansinanea A; Lecomte MC; Dhermy D; Boivin P Medicina (B Aires); 1992; 52(2):109-15. PubMed ID: 1308902 [TBL] [Abstract][Full Text] [Related]
49. Hereditary elliptocytosis with a spectrin molecular defect in a white patient. Lecomte MC; Dhermy D; Garbarz M; Gautero H; Bournier O; Galand C; Boivin P Acta Haematol; 1984; 71(4):235-40. PubMed ID: 6426236 [TBL] [Abstract][Full Text] [Related]
50. Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemia. Dhermy D; Lecomte MC; Garbarz M; Feo C; Gautero H; Bournier O; Galand C; Herrera A; Gretillat F; Boivin P Pediatr Res; 1984 Oct; 18(10):1005-12. PubMed ID: 6493844 [TBL] [Abstract][Full Text] [Related]
51. Dependence of the permanent deformation of red blood cell membranes on spectrin dimer-tetramer equilibrium: implication for permanent membrane deformation of irreversibly sickled cells. Liu SC; Derick LH; Palek J Blood; 1993 Jan; 81(2):522-8. PubMed ID: 8422468 [TBL] [Abstract][Full Text] [Related]
52. A case of elliptocytosis associated with a truncated spectrin chain. Ohanian V; Evans JP; Gratzer WB Br J Haematol; 1985 Sep; 61(1):31-9. PubMed ID: 4052329 [TBL] [Abstract][Full Text] [Related]
53. Structural determinants of the rigidity of the red cell membrane. Nash GB; Gratzer WB Biorheology; 1993; 30(5-6):397-407. PubMed ID: 8186406 [TBL] [Abstract][Full Text] [Related]
54. Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton. Wandersee NJ; Birkenmeier CS; Bodine DM; Mohandas N; Barker JE Blood; 2003 Jan; 101(1):325-30. PubMed ID: 12393645 [TBL] [Abstract][Full Text] [Related]
55. Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1. Conboy JG; Shitamoto R; Parra M; Winardi R; Kabra A; Smith J; Mohandas N Blood; 1991 Nov; 78(9):2438-43. PubMed ID: 1932756 [TBL] [Abstract][Full Text] [Related]
56. [Cytoskeleton anomalies in disorders of red cell membrane proteins]. Kanzaki A; Wada H; Yawata Y Rinsho Ketsueki; 1991 Jun; 32(6):573-9. PubMed ID: 1832469 [TBL] [Abstract][Full Text] [Related]
57. Elliptocytosis-associated spectrin Rouen (beta 220/218) has a truncated but still phosphorylatable beta chain. Lecomte MC; Gautero H; Bournier O; Galand C; Lahary A; Vannier JP; Garbarz M; Delaunay J; Tchernia G; Boivin P Br J Haematol; 1992 Feb; 80(2):242-50. PubMed ID: 1550783 [TBL] [Abstract][Full Text] [Related]
58. Molecular heterogeneity of hereditary elliptocytosis in Italy. Miraglia del Giudice E; Perrotta S; Sannino E; De Angelis F; Nobili B; Iolascon A Haematologica; 1994; 79(5):400-5. PubMed ID: 7843625 [TBL] [Abstract][Full Text] [Related]
59. Spectrin modifications in a heterozygous case of both hereditary elliptocytosis and beta-thalassemia. Streichman S; Herz E; Tatarsky I Am J Hematol; 1990 Feb; 33(2):123-7. PubMed ID: 2301371 [TBL] [Abstract][Full Text] [Related]
60. Cytoskeleton influence on normal and tangent fluctuation modes in the red blood cells. Rochal SB; Lorman VL Phys Rev Lett; 2006 Jun; 96(24):248102. PubMed ID: 16907283 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]