515 related articles for article (PubMed ID: 6215583)
1. A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.
Wolfe LC; John KM; Falcone JC; Byrne AM; Lux SE
N Engl J Med; 1982 Nov; 307(22):1367-74. PubMed ID: 6215583
[TBL] [Abstract][Full Text] [Related]
2. Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis.
Goodman SR; Shiffer KA; Casoria LA; Eyster ME
Blood; 1982 Sep; 60(3):772-84. PubMed ID: 7104494
[TBL] [Abstract][Full Text] [Related]
3. Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis.
Marík T; Kselíková M; Bíbr B; Brabec V; Lener J
Folia Haematol Int Mag Klin Morphol Blutforsch; 1983; 110(1):81-5. PubMed ID: 6192057
[TBL] [Abstract][Full Text] [Related]
4. Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.
Becker PS; Tse WT; Lux SE; Forget BG
J Clin Invest; 1993 Aug; 92(2):612-6. PubMed ID: 8102379
[TBL] [Abstract][Full Text] [Related]
5. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
Eber SW
Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935
[TBL] [Abstract][Full Text] [Related]
6. Hereditary spherocytosis of man. Altered binding of cytoskeletal components to the erythrocyte membrane.
Hill JS; Sawyer WH; Howlett GJ; Wiley JS
Biochem J; 1982 Feb; 201(2):259-66. PubMed ID: 7082289
[TBL] [Abstract][Full Text] [Related]
7. [Molecular interactions of membrane proteins and erythrocyte deformability].
Boivin P
Pathol Biol (Paris); 1984 Jun; 32(6):717-35. PubMed ID: 6235477
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis.
Zail SS; Coetzer TL
J Clin Invest; 1984 Sep; 74(3):753-62. PubMed ID: 6236232
[TBL] [Abstract][Full Text] [Related]
10. Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.
Becker PS; Morrow JS; Lux SE
J Clin Invest; 1987 Aug; 80(2):557-65. PubMed ID: 3611357
[TBL] [Abstract][Full Text] [Related]
11. Erythrocyte membrane skeletal protein 4.1: a brief review.
Goodman SR; Shiffer K; Coleman DB; Whitfield CF
Prog Clin Biol Res; 1984; 165():415-39. PubMed ID: 6390456
[No Abstract] [Full Text] [Related]
12. Studies on human erythrocyte spectrin.4.1.actin complex with the use of cytochalasins.
Lin DC
Prog Clin Biol Res; 1981; 56():117-36. PubMed ID: 7330006
[No Abstract] [Full Text] [Related]
13. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.
Lux SE; Tse WT; Menninger JC; John KM; Harris P; Shalev O; Chilcote RR; Marchesi SL; Watkins PC; Bennett V
Nature; 1990 Jun; 345(6277):736-9. PubMed ID: 2141669
[TBL] [Abstract][Full Text] [Related]
14. Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis.
Hassoun H; Vassiliadis JN; Murray J; Yi SJ; Hanspal M; Ware RE; Winter SS; Chiou SS; Palek J
J Clin Invest; 1995 Dec; 96(6):2623-9. PubMed ID: 8675627
[TBL] [Abstract][Full Text] [Related]
15. Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.
Costa FF; Agre P; Watkins PC; Winkelmann JC; Tang TK; John KM; Lux SE; Forget BG
N Engl J Med; 1990 Oct; 323(15):1046-50. PubMed ID: 1977081
[No Abstract] [Full Text] [Related]
16. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis].
Ferrándiz F; Ródenas S; Villegas A
Sangre (Barc); 1993 Oct; 38(5):393-7. PubMed ID: 8140503
[TBL] [Abstract][Full Text] [Related]
17. Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.
Coetzer TL; Lawler J; Liu SC; Prchal JT; Gualtieri RJ; Brain MC; Dacie JV; Palek J
N Engl J Med; 1988 Jan; 318(4):230-4. PubMed ID: 2961992
[No Abstract] [Full Text] [Related]
18. Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton.
Lorenzo F; Dalla Venezia N; Morlé L; Baklouti F; Alloisio N; Ducluzeau MT; Roda L; Lefrançois P; Delaunay J
J Clin Invest; 1994 Oct; 94(4):1651-6. PubMed ID: 7929842
[TBL] [Abstract][Full Text] [Related]
19. Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane.
Rybicki AC; Heath R; Wolf JL; Lubin B; Schwartz RS
J Clin Invest; 1988 Mar; 81(3):893-901. PubMed ID: 2963832
[TBL] [Abstract][Full Text] [Related]
20. The molecular basis for membrane - cytoskeleton association in human erythrocytes.
Bennett V
J Cell Biochem; 1982; 18(1):49-65. PubMed ID: 6461664
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
