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 *

273 related articles for article (PubMed ID: 8808627)

  • 1. 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]  

  • 2. Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice.
    Peters LL; Jindel HK; Gwynn B; Korsgren C; John KM; Lux SE; Mohandas N; Cohen CM; Cho MR; Golan DE; Brugnara C
    J Clin Invest; 1999 Jun; 103(11):1527-37. PubMed ID: 10359562
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Modeling of band-3 protein diffusion in the normal and defective red blood cell membrane.
    Li H; Zhang Y; Ha V; Lykotrafitis G
    Soft Matter; 2016 Apr; 12(15):3643-53. PubMed ID: 26977476
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Trafficking and folding defects in hereditary spherocytosis mutants of the human red cell anion exchanger.
    Quilty JA; Reithmeier RA
    Traffic; 2000 Dec; 1(12):987-98. PubMed ID: 11208088
    [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. Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts.
    Satchwell TJ; Bell AJ; Hawley BR; Pellegrin S; Mordue KE; van Deursen CT; Braak NH; Huls G; Leers MP; Overwater E; Tamminga RY; van der Zwaag B; Fermo E; Bianchi P; van Wijk R; Toye AM
    Haematologica; 2016 Sep; 101(9):1018-27. PubMed ID: 27247322
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Protein 4.2 interaction with hereditary spherocytosis mutants of the cytoplasmic domain of human anion exchanger 1.
    Bustos SP; Reithmeier RA
    Biochem J; 2011 Jan; 433(2):313-22. PubMed ID: 21039340
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ubiquitylation-independent ER-associated degradation of an AE1 mutant associated with dominant hereditary spherocytosis in cattle.
    Ito D; Koshino I; Arashiki N; Adachi H; Tomihari M; Tamahara S; Kurogi K; Amano T; Ono K; Inaba M
    J Cell Sci; 2006 Sep; 119(Pt 17):3602-12. PubMed ID: 16912075
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton.
    Southgate CD; Chishti AH; Mitchell B; Yi SJ; Palek J
    Nat Genet; 1996 Oct; 14(2):227-30. PubMed ID: 8841202
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Erythrocyte membrane skeleton abnormalities in hereditary spherocytosis.
    Burke BE; Shotton DM
    Br J Haematol; 1983 Jun; 54(2):173-87. PubMed ID: 6849841
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The cytoskeletal binding domain of band 3 is required for multiprotein complex formation and retention during erythropoiesis.
    Satchwell TJ; Hawley BR; Bell AJ; Ribeiro ML; Toye AM
    Haematologica; 2015 Jan; 100(1):133-42. PubMed ID: 25344524
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular basis of altered red blood cell membrane properties in Southeast Asian ovalocytosis: role of the mutant band 3 protein in band 3 oligomerization and retention by the membrane skeleton.
    Liu SC; Palek J; Yi SJ; Nichols PE; Derick LH; Chiou SS; Amato D; Corbett JD; Cho MR; Golan DE
    Blood; 1995 Jul; 86(1):349-58. PubMed ID: 7795244
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hemolytic anemias due to disorders of red cell membrane skeleton.
    Bossi D; Russo M
    Mol Aspects Med; 1996 Apr; 17(2):171-88. PubMed ID: 8813717
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.
    Wolfe LC; John KM; Falcone JC; Byrne AM; Lux SE
    N Engl J Med; 1982 Nov; 307(22):1367-74. PubMed ID: 6215583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Full-Length Anion Exchanger 1 Structure and Interactions with Ankyrin-1 Determined by Zero Length Crosslinking of Erythrocyte Membranes.
    Rivera-Santiago R; Harper SL; Sriswasdi S; Hembach P; Speicher DW
    Structure; 2017 Jan; 25(1):132-145. PubMed ID: 27989623
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.