843 related articles for article (PubMed ID: 11418000)
1. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?
Giorgi M; Cianci CD; Gallagher PG; Morrow JS
Exp Mol Pathol; 2001 Jun; 70(3):215-30. PubMed ID: 11418000
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Interactions of spectrin in hereditary elliptocytes containing truncated spectrin beta-chains.
Eber SW; Morris SA; Schröter W; Gratzer WB
J Clin Invest; 1988 Feb; 81(2):523-30. PubMed ID: 3276733
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. The genetic disorders of the red cell skeleton.
Delaunay J; Alloisio N; Morle L; Baklouti F
Nouv Rev Fr Hematol (1978); 1991; 33(2):63-70. PubMed ID: 1766857
[TBL] [Abstract][Full Text] [Related]
6. Phosphorylation of ankyrin down-regulates its cooperative interaction with spectrin and protein 3.
Cianci CD; Giorgi M; Morrow JS
J Cell Biochem; 1988 Jul; 37(3):301-15. PubMed ID: 2970468
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
Garbarz M; Bibas D; Cynober T; Galand C; Bournier O; Devaux I; Tchernia G; Dhermy D
C R Acad Sci III; 1996 Oct; 319(10):913-9. PubMed ID: 8977772
[TBL] [Abstract][Full Text] [Related]
9. Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
Tse WT; Lecomte MC; Costa FF; Garbarz M; Feo C; Boivin P; Dhermy D; Forget BG
J Clin Invest; 1990 Sep; 86(3):909-16. PubMed ID: 1975598
[TBL] [Abstract][Full Text] [Related]
10. Mapping of an ankyrin-sensitive, phosphatidylethanolamine/phosphatidylcholine mono- and bi-layer binding site in erythroid beta-spectrin.
Hryniewicz-Jankowska A; Bok E; Dubielecka P; Chorzalska A; Diakowski W; Jezierski A; Lisowski M; Sikorski AF
Biochem J; 2004 Sep; 382(Pt 2):677-85. PubMed ID: 15171729
[TBL] [Abstract][Full Text] [Related]
11. Ankyrin and synapsin: spectrin-binding proteins associated with brain membranes.
Bennett V; Baines AJ; Davis JQ
J Cell Biochem; 1985; 29(2):157-69. PubMed ID: 2933418
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Structural insight into an ankyrin-sensitive lipid-binding site of erythroid beta-spectrin.
Czogalla A; Jaszewski AR; Diakowski W; Bok E; Jezierski A; Sikorski AF
Mol Membr Biol; 2007; 24(3):215-24. PubMed ID: 17520478
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Studies of the erythrocyte spectrin tetramerization region.
Park S; Mehboob S; Luo BH; Hurtuk M; Johnson ME; Fung LW
Cell Mol Biol Lett; 2001; 6(3):571-85. PubMed ID: 11598635
[TBL] [Abstract][Full Text] [Related]
16. Hemolytic anemias associated with deficient or dysfunctional spectrin.
Lux SE; Pease B; Tomaselli MB; John KM; Bernstein SE
Prog Clin Biol Res; 1979; 30():463-9. PubMed ID: 531037
[TBL] [Abstract][Full Text] [Related]
17. A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.
Gallagher PG; Tse WT; Coetzer T; Lecomte MC; Garbarz M; Zarkowsky HS; Baruchel A; Ballas SK; Dhermy D; Palek J
J Clin Invest; 1992 Mar; 89(3):892-8. PubMed ID: 1541680
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Red cell membrane polypeptides under normal conditions and in genetic disorders.
Delaunay J
Transfus Clin Biol; 1995; 2(4):207-16. PubMed ID: 8542017
[TBL] [Abstract][Full Text] [Related]
20. Hemolytic anemias due to abnormalities in red cell spectrin: a brief review.
Lux SE; Wolfe LC; Pease B; Tomaselli MB; John KM; Bernstein SE
Prog Clin Biol Res; 1981; 45():159-68. PubMed ID: 7017750
[No Abstract] [Full Text] [Related]
[Next] [New Search]
