BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 8943874)

  • 1. 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]  

  • 2. 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]  

  • 3. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population.
    Yawata Y; Kanzaki A; Yawata A; Doerfler W; Ozcan R; Eber SW
    Int J Hematol; 2000 Feb; 71(2):118-35. PubMed ID: 10745622
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.
    Jenkins PB; Abou-Alfa GK; Dhermy D; Bursaux E; Féo C; Scarpa AL; Lux SE; Garbarz M; Forget BG; Gallagher PG
    J Clin Invest; 1996 Jan; 97(2):373-80. PubMed ID: 8567957
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Band 3 deficiency as a cause of hereditary spherocytosis].
    Wada H; Suemori S; Nakanishi H; Sugihara T
    Rinsho Ketsueki; 2015 Jul; 56(7):837-45. PubMed ID: 26251147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.
    Hassoun H; Vassiliadis JN; Murray J; Njolstad PR; Rogus JJ; Ballas SK; Schaffer F; Jarolim P; Brabec V; Palek J
    Blood; 1997 Jul; 90(1):398-406. PubMed ID: 9207476
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects.
    Dhermy D; Galand C; Bournier O; Boulanger L; Cynober T; Schismanoff PO; Bursaux E; Tchernia G; Boivin P; Garbarz M
    Br J Haematol; 1997 Jul; 98(1):32-40. PubMed ID: 9233560
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Hereditary spherocytosis with spectrin deficiency related to null mutations of the beta-spectrin gene.
    Dhermy D; Galand C; Bournier O; Cynober T; Méchinaud F; Tchemia G; Garbarz M
    Blood Cells Mol Dis; 1998 Jun; 24(2):251-61. PubMed ID: 9714702
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Band 3 Cape Town (E90K) causes severe hereditary spherocytosis in combination with band 3 Prague III.
    Bracher NA; Lyons CA; Wessels G; Mansvelt E; Coetzer TL
    Br J Haematol; 2001 Jun; 113(3):689-93. PubMed ID: 11380459
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ankyrin gene mutations in japanese patients with hereditary spherocytosis.
    Nakanishi H; Kanzaki A; Yawata A; Yamada O; Yawata Y
    Int J Hematol; 2001 Jan; 73(1):54-63. PubMed ID: 11372755
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Simultaneous (AC)n microsatellite polymorphism analysis and single-stranded conformation polymorphism screening is an efficient strategy for detecting ankyrin-1 mutations in dominant hereditary spherocytosis.
    Ozcan R; Jarolim P; Lux SE; Ungewickell E; Eber SW
    Br J Haematol; 2003 Aug; 122(4):669-77. PubMed ID: 12899723
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
    Eber SW; Gonzalez JM; Lux ML; Scarpa AL; Tse WT; Dornwell M; Herbers J; Kugler W; Ozcan R; Pekrun A; Gallagher PG; Schröter W; Forget BG; Lux SE
    Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil.
    Saad ST; Costa FF; Vicentim DL; Salles TS; Pranke PH
    Br J Haematol; 1994 Oct; 88(2):295-9. PubMed ID: 7803273
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Band 3 Campinas: a novel splicing mutation in the band 3 gene (AE1) associated with hereditary spherocytosis, hyperactivity of Na+/Li+ countertransport and an abnormal renal bicarbonate handling.
    Lima PR; Gontijo JA; Lopes de Faria JB; Costa FF; Saad ST
    Blood; 1997 Oct; 90(7):2810-8. PubMed ID: 9326249
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The red blood cell band 3 variant (band 3Biceêtrel:R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negative effect.
    Dhermy D; Burnier O; Bourgeois M; Grandchamp B
    Mol Membr Biol; 1999; 16(4):305-12. PubMed ID: 10766130
    [TBL] [Abstract][Full Text] [Related]  

  • 20. beta-Spectrin São PauloII, a novel frameshift mutation of the beta-spectrin gene associated with hereditary spherocytosis and instability of the mutant mRNA.
    Bassères DS; Tavares AC; Costa FF; Saad ST
    Braz J Med Biol Res; 2002 Aug; 35(8):921-5. PubMed ID: 12185384
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.