These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 8547122)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosis.
    Bianchi P; Zanella A; Alloisio N; Barosi G; Bredi E; Pelissero G; Zappa M; Vercellati C; Baronciani L; Delaunay J; Sirchia G
    Br J Haematol; 1997 Aug; 98(2):283-8. PubMed ID: 9266920
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Hereditary spherocytosis associated with protein band 3 defect in a Swiss kindred.
    Reinhart WH; Wyss EJ; Arnold D; Ott P
    Br J Haematol; 1994 Jan; 86(1):147-55. PubMed ID: 8011524
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.