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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. Combination of hereditary elliptocytosis and hereditary spherocytosis. Aksoy M; Erdem S; Dincol G; Erdogan G; Cilingiroglu K; Dincol K Clin Genet; 1974; 6(1):46-50. PubMed ID: 4426130 [No Abstract] [Full Text] [Related]
7. Inherited hemolytic disease in mice: a review and update. Bernstein SE Lab Anim Sci; 1980 Apr; 30(2 Pt 1):197-205. PubMed ID: 6763106 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Beta-spectrinBari: a truncated beta-chain responsible for dominant hereditary spherocytosis. Perrotta S; Della Ragione F; Rossi F; Avvisati RA; Di Pinto D; De Mieri G; Scianguetta S; Mancusi S; De Falco L; Marano V; Iolascon A Haematologica; 2009 Dec; 94(12):1753-7. PubMed ID: 19608679 [TBL] [Abstract][Full Text] [Related]
10. [Progress in research on red cell membrane disorders: from the genome to the postgenome era]. Yawata Y Rinsho Ketsueki; 2001 May; 42(5):343-51. PubMed ID: 11452448 [No Abstract] [Full Text] [Related]
11. [Hemolytic anemia caused by congenital anomalies of the erythrocyte membrane]. Boivin P J Genet Hum; 1986 Nov; 34(5):393-412. PubMed ID: 3540209 [No Abstract] [Full Text] [Related]
12. 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]
13. Update on the clinical spectrum and genetics of red blood cell membrane disorders. Gallagher PG Curr Hematol Rep; 2004 Mar; 3(2):85-91. PubMed ID: 14965483 [TBL] [Abstract][Full Text] [Related]
14. Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man. Birkenmeier CS; McFarland-Starr EC; Barker JE Proc Natl Acad Sci U S A; 1988 Nov; 85(21):8121-5. PubMed ID: 3186715 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. Novel beta-spectrin mutations in hereditary spherocytosis associated with decreased levels of mRNA. Maciag M; Płochocka D; Adamowicz-Salach A; Burzyńska B Br J Haematol; 2009 Aug; 146(3):326-32. PubMed ID: 19538529 [TBL] [Abstract][Full Text] [Related]
18. Identification of a Novel Mutation of β-Spectrin in Hereditary Spherocytosis Using Whole Exome Sequencing. Bogusławska DM; Skulski M; Machnicka B; Potoczek S; Kraszewski S; Kuliczkowski K; Sikorski AF Int J Mol Sci; 2021 Oct; 22(20):. PubMed ID: 34681667 [TBL] [Abstract][Full Text] [Related]
19. Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer. Eber S; Lux SE Semin Hematol; 2004 Apr; 41(2):118-41. PubMed ID: 15071790 [TBL] [Abstract][Full Text] [Related]