BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 11380459)

  • 1. 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]  

  • 2. 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]  

  • 3. Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas).
    Alloisio N; Maillet P; Carré G; Texier P; Vallier A; Baklouti F; Philippe N; Delaunay J
    Blood; 1996 Aug; 88(3):1062-9. PubMed ID: 8704215
    [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. Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11.
    Maillet P; Vallier A; Reinhart WH; Wyss EJ; Ott P; Texier P; Baklouti F; Tanner MJ; Delaunay J; Alloisio N
    Br J Haematol; 1995 Dec; 91(4):804-10. PubMed ID: 8547122
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 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. 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]  

  • 9. Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis.
    Kanzaki A; Hayette S; Morlé L; Inoue F; Matsuyama R; Inoue T; Yawata A; Wada H; Vallier A; Alloisio N; Yawata Y; Delaunay J
    Br J Haematol; 1997 Dec; 99(3):522-30. PubMed ID: 9401060
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis.
    Alloisio N; Texier P; Vallier A; Ribeiro ML; Morlé L; Bozon M; Bursaux E; Maillet P; Gonçalves P; Tanner MJ; Tamagnini G; Delaunay J
    Blood; 1997 Jul; 90(1):414-20. PubMed ID: 9207478
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary spherocytosis (HS) due to loss of anion exchange transporter.
    Iolascon A; Miraglia del Giudice E; Perrotta S; Pinto L; Fiorelli G; Cappellini DM; Vasseur C; Bursaux E; Cutillo S
    Haematologica; 1992; 77(6):450-6. PubMed ID: 1289181
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Band 3Tambaú: a de novo mutation in the AE1 gene associated with hereditary spherocytosis. Implications for anion exchange and insertion into the red blood cell membrane.
    Lima PR; Baratti MO; Chiattone ML; Costa FF; Saad ST
    Eur J Haematol; 2005 May; 74(5):396-401. PubMed ID: 15813913
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 Vesuvio.
    Perrotta S; Polito F; Cone ML; Nobili B; Cutillo S; Nigro V; Iolascon A; Amendola G
    Blood; 1999 Mar; 93(6):2131-2. PubMed ID: 10189204
    [No Abstract]   [Full Text] [Related]  

  • 14. Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locus.
    Miraglia del Giudice E; Vallier A; Maillet P; Perrotta S; Cutillo S; Iolascon A; Tanner MJ; Delaunay J; Alloisio N
    Br J Haematol; 1997 Jan; 96(1):70-6. PubMed ID: 9012689
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Band 3 Tokyo: Thr837-->Ala837 substitution in erythrocyte band 3 protein associated with spherocytic hemolysis.
    Iwase S; Ideguchi H; Takao M; Horiguchi-Yamada J; Iwasaki M; Takahara S; Sekikawa T; Mochizuki S; Yamada H
    Acta Haematol; 1998; 100(4):200-3. PubMed ID: 9973643
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1.
    Van Zwieten R; François JJ; Van Leeuwen K; Van Wesel AC; Van Bruggen R; Van Solinge WW; Roos D; Verhoeven AJ; Van Wijk R
    Am J Hematol; 2013 Feb; 88(2):159-60. PubMed ID: 23255290
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis.
    van Zwieten R; van Oirschot BA; Veldthuis M; Dobbe JG; Streekstra GJ; van Solinge WW; Schutgens RE; van Wijk R
    Am J Hematol; 2015 Mar; 90(3):E35-9. PubMed ID: 25388786
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.