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6. A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred. Costa DB; Lozovatsky L; Gallagher PG; Forget BG Blood; 2005 Dec; 106(13):4367-9. PubMed ID: 16150946 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis. Sahr KE; Tobe T; Scarpa A; Laughinghouse K; Marchesi SL; Agre P; Linnenbach AJ; Marchesi VT; Forget BG J Clin Invest; 1989 Oct; 84(4):1243-52. PubMed ID: 2794061 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Dizygotic twins with prolonged jaundice and microcytic, hypochromic, hemolytic anemia with pyropoikilocytosis. Bahr TM; Lozano-Chinga M; Agarwal AM; Meznarich JA; Gerday E; Smoot JL; Taylor A; Christensen RD Blood Cells Mol Dis; 2020 Nov; 85():102462. PubMed ID: 32623341 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Molecular genetics of the human beta-spectrin gene. Forget BG; Chang JG; Coupal E; Stanislovitis P; Costa FF; Winkelmann JC; Agre PC; Marchesi VT; Watkins PC Trans Assoc Am Physicians; 1988; 101():149-54. PubMed ID: 2908371 [No Abstract] [Full Text] [Related]
14. The murine mutation jaundiced is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of beta-spectrin. Bloom ML; Kaysser TM; Birkenmeier CS; Barker JE Proc Natl Acad Sci U S A; 1994 Oct; 91(21):10099-103. PubMed ID: 7937844 [TBL] [Abstract][Full Text] [Related]
16. Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes. Bodine DM; Birkenmeier CS; Barker JE Cell; 1984 Jul; 37(3):721-9. PubMed ID: 6234993 [TBL] [Abstract][Full Text] [Related]
17. Transient, localized accumulation of alpha-spectrin during sea urchin morphogenesis. Wessel GM; Chen SW Dev Biol; 1993 Jan; 155(1):161-71. PubMed ID: 8416831 [TBL] [Abstract][Full Text] [Related]
18. Clinical expression of alpha spectrin mutants in hereditary elliptocytosis. Palek J; Coetzer T Blood Cells; 1987; 13(1-2):237-50. PubMed ID: 3311220 [TBL] [Abstract][Full Text] [Related]
19. [Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry]. Dhermy D; Féo C; Garbarz M; Bournier O; Dommergues JP; Garcia J; Boivin P; Tchernia G Nouv Rev Fr Hematol (1978); 1983; 25(1):7-16. PubMed ID: 6835836 [TBL] [Abstract][Full Text] [Related]
20. Alpha128 Arg-->Ser (CGT-->AGT) spectrin mutation associated with severe neonatal elliptopoikilocytosis in Spain. Corrons JL; Pujades A; Alvarez R; Estella J; Dhermy D Haematologica; 2001 May; 86(5):537-8. PubMed ID: 11410419 [No Abstract] [Full Text] [Related] [Next] [New Search]