BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 17112522)

  • 1. Characterization of red cell membrane proteins as a function of red cell density: annexin VII in different forms of hereditary spherocytosis.
    Caterino M; Ruoppolo M; Orrù S; Savoia M; Perrotta S; Del Vecchio L; Salvatore F; Stewart GW; Iolascon A
    FEBS Lett; 2006 Dec; 580(28-29):6527-32. PubMed ID: 17112522
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects.
    De Franceschi L; Olivieri O; Miraglia del Giudice E; Perrotta S; Sabato V; Corrocher R; Iolascon A
    Am J Hematol; 1997 Jul; 55(3):121-8. PubMed ID: 9256290
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases.
    Ricard MP; Gilsanz F; Millan I
    Haematologica; 2000 Sep; 85(9):994-5. PubMed ID: 10980645
    [No Abstract]   [Full Text] [Related]  

  • 6. Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning role.
    Ingrosso D; D'Angelo S; Perrotta S; d'Urzo G; Iolascon A; Perna AF; Galletti P; Zappia V; Miraglia del Giudice E
    Br J Haematol; 1996 Apr; 93(1):38-41. PubMed ID: 8611472
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [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]  

  • 9. Combined ankyrin and spectrin deficiency in hereditary spherocytosis.
    Pekrun A; Eber SW; Kuhlmey A; Schröter W
    Ann Hematol; 1993 Aug; 67(2):89-93. PubMed ID: 8347735
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population.
    Ayhan AC; Yildiz I; Yüzbaşıoğlu S; Celkan T; Apak H; Ozkan A; Karaman S
    Hematology; 2012 Jul; 17(4):232-6. PubMed ID: 22889517
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis.
    Lee YK; Cho HI; Park SS; Lee YJ; Ra E; Chang YH; Hur M; Shin HY; Ahn HS
    J Korean Med Sci; 2000 Jun; 15(3):284-8. PubMed ID: 10895969
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary spherocytosis: identification of several HS families with ankyrin and band 3 deficiency in a population of southwestern Poland.
    Bogusławska DM; Heger E; Chorzalska A; Nierzwicka M; Hołojda J; Swiderska A; Straburzyńska A; Paździor G; Langner M; Sikorski AF
    Ann Hematol; 2004 Jan; 83(1):28-33. PubMed ID: 14517693
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients.
    Rocha S; Costa E; Rocha-Pereira P; Ferreira F; Cleto E; Barbot J; Quintanilha A; Belo L; Santos-Silva A
    Br J Haematol; 2010 Jun; 149(5):785-94. PubMed ID: 20346007
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Characteristics of hereditary spherocytosis].
    Yawata Y
    Nihon Naika Gakkai Zasshi; 1999 Sep; 88(9):1825-33. PubMed ID: 10581770
    [No Abstract]   [Full Text] [Related]  

  • 16. Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.
    Inoue T; Kanzaki A; Yawata A; Wada H; Okamoto N; Takahashi M; Sugihara T; Yamada O; Yawata Y
    Int J Hematol; 1994 Dec; 60(4):227-38. PubMed ID: 7894027
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Application of 2 electrophoresis techniques to the analysis of erythrocyte membrane proteins in hereditary spherocytosis].
    Ferrándiz F; Ródenas S; Villegas A
    Sangre (Barc); 1993 Oct; 38(5):393-7. PubMed ID: 8140503
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis.
    Miraglia del Giudice E; Iolascon A; Pinto L; Nobili B; Perrotta S
    Br J Haematol; 1994 Sep; 88(1):52-5. PubMed ID: 7803256
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
    Garbarz M; Bibas D; Cynober T; Galand C; Bournier O; Devaux I; Tchernia G; Dhermy D
    C R Acad Sci III; 1996 Oct; 319(10):913-9. PubMed ID: 8977772
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.