232 related articles for article (PubMed ID: 20056793)
1. Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells.
Robledo RF; Lambert AJ; Birkenmeier CS; Cirlan MV; Cirlan AF; Campagna DR; Lux SE; Peters LL
Blood; 2010 Mar; 115(9):1804-14. PubMed ID: 20056793
[TBL] [Abstract][Full Text] [Related]
2. Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene.
Wandersee NJ; Birkenmeier CS; Gifford EJ; Mohandas N; Barker JE
Hematol J; 2000; 1(4):235-42. PubMed ID: 11920196
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.
Jarolim P; Murray JL; Rubin HL; Taylor WM; Prchal JT; Ballas SK; Snyder LM; Chrobak L; Melrose WD; Brabec V; Palek J
Blood; 1996 Dec; 88(11):4366-74. PubMed ID: 8943874
[TBL] [Abstract][Full Text] [Related]
5. Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia.
Wichterle H; Hanspal M; Palek J; Jarolim P
J Clin Invest; 1996 Nov; 98(10):2300-7. PubMed ID: 8941647
[TBL] [Abstract][Full Text] [Related]
6. Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiency.
Peters LL; Swearingen RA; Andersen SG; Gwynn B; Lambert AJ; Li R; Lux SE; Churchill GA
Blood; 2004 Apr; 103(8):3233-40. PubMed ID: 15070709
[TBL] [Abstract][Full Text] [Related]
7. Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation.
Inaba M; Yawata A; Koshino I; Sato K; Takeuchi M; Takakuwa Y; Manno S; Yawata Y; Kanzaki A; Sakai J; Ban A; Ono K; Maede Y
J Clin Invest; 1996 Apr; 97(8):1804-17. PubMed ID: 8621763
[TBL] [Abstract][Full Text] [Related]
8. Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis.
Wandersee NJ; Roesch AN; Hamblen NR; de Moes J; van der Valk MA; Bronson RT; Gimm JA; Mohandas N; Demant P; Barker JE
Blood; 2001 Jan; 97(2):543-50. PubMed ID: 11154235
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Combined deletion of mouse dematin-headpiece and beta-adducin exerts a novel effect on the spectrin-actin junctions leading to erythrocyte fragility and hemolytic anemia.
Chen H; Khan AA; Liu F; Gilligan DM; Peters LL; Messick J; Haschek-Hock WM; Li X; Ostafin AE; Chishti AH
J Biol Chem; 2007 Feb; 282(6):4124-35. PubMed ID: 17142833
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis.
Reliene R; Mariani M; Zanella A; Reinhart WH; Ribeiro ML; del Giudice EM; Perrotta S; Iolascon A; Eber S; Lutz HU
Blood; 2002 Sep; 100(6):2208-15. PubMed ID: 12200387
[TBL] [Abstract][Full Text] [Related]
14. Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis.
Jarolim P; Rubin HL; Brabec V; Chrobak L; Zolotarev AS; Alper SL; Brugnara C; Wichterle H; Palek J
Blood; 1995 Feb; 85(3):634-40. PubMed ID: 7530501
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Molecular aspects of erythrocyte membrane disorders].
Saad ST; Costa FF
Rev Assoc Med Bras (1992); 1994; 40(3):216-24. PubMed ID: 7787875
[No Abstract] [Full Text] [Related]
17. Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin.
Hassoun H; Vassiliadis JN; Murray J; Yi SJ; Hanspal M; Johnson CA; Palek J
Blood; 1996 Mar; 87(6):2538-45. PubMed ID: 8630421
[TBL] [Abstract][Full Text] [Related]
18. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
Tshilolo L; Kagambega F; Sztern B; Vertongen F; Gulbis B
Rev Med Brux; 1998 Oct; 19(5 Pt 1):417-23. PubMed ID: 9844481
[TBL] [Abstract][Full Text] [Related]
19. Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).
Jarolim P; Rubin HL; Liu SC; Cho MR; Brabec V; Derick LH; Yi SJ; Saad ST; Alper S; Brugnara C
J Clin Invest; 1994 Jan; 93(1):121-30. PubMed ID: 8282779
[TBL] [Abstract][Full Text] [Related]
20. Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton.
Peters LL; Shivdasani RA; Liu SC; Hanspal M; John KM; Gonzalez JM; Brugnara C; Gwynn B; Mohandas N; Alper SL; Orkin SH; Lux SE
Cell; 1996 Sep; 86(6):917-27. PubMed ID: 8808627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
