BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

255 related articles for article (PubMed ID: 29623813)

  • 1. Analysis of erythrocyte membrane proteins in patients with hereditary spherocytosis and other types of haemolytic anaemia.
    Shibuya A; Kawashima H; Tanaka M
    Hematology; 2018 Oct; 23(9):669-675. PubMed ID: 29623813
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Efficacy of cytochemical tests in gene analysis of hereditary spherocytosis: a case study of six patients with different disease subtypes.
    Shibuya A; Kawashima H; Tanaka M
    Hematology; 2021 Dec; 26(1):827-834. PubMed ID: 34672909
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Hereditary spherocytosis.
    Perrotta S; Gallagher PG; Mohandas N
    Lancet; 2008 Oct; 372(9647):1411-26. PubMed ID: 18940465
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect.
    Mariani M; Barcellini W; Vercellati C; Marcello AP; Fermo E; Pedotti P; Boschetti C; Zanella A
    Haematologica; 2008 Sep; 93(9):1310-7. PubMed ID: 18641031
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations.
    Margetis P; Antonelou M; Karababa F; Loutradi A; Margaritis L; Papassideri I
    Blood Cells Mol Dis; 2007; 38(3):210-20. PubMed ID: 17208471
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
    Trabelsi N; Bouguerra G; Haddad F; Ouederni M; Darragi I; Boudrigua I; Chaouachi D; Barmat M; Fouzai C; Bejaoui M; Menif S; Kraiem I; Abbes S
    Cell Physiol Biochem; 2021 Mar; 55(1):117-129. PubMed ID: 33667330
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy.
    Li Y; Lu L; Li J
    Cell Biochem Biophys; 2016 Sep; 74(3):365-71. PubMed ID: 27557951
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next‑generation sequencing technology and matrix‑assisted laser desorption/ionization time‑of‑flight mass spectrometry.
    Şener LT; Aktan M; Albeniz G; Şener A; Üstek D; Albeniz I
    Mol Med Rep; 2019 May; 19(5):3912-3922. PubMed ID: 30896804
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary spherocytosis and related disorders.
    Becker PS; Lux SE
    Clin Haematol; 1985 Feb; 14(1):15-43. PubMed ID: 3886234
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis.
    Goodman SR; Shiffer KA; Casoria LA; Eyster ME
    Blood; 1982 Sep; 60(3):772-84. PubMed ID: 7104494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary spherocytosis of man. Altered binding of cytoskeletal components to the erythrocyte membrane.
    Hill JS; Sawyer WH; Howlett GJ; Wiley JS
    Biochem J; 1982 Feb; 201(2):259-66. PubMed ID: 7082289
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The abnormal phosphorylation of spectrin in human hereditary spherocytosis.
    Thompson S; Maddy AH
    Biochim Biophys Acta; 1981 Nov; 649(1):31-7. PubMed ID: 6272858
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.
    King MJ; Telfer P; MacKinnon H; Langabeer L; McMahon C; Darbyshire P; Dhermy D
    Cytometry B Clin Cytom; 2008 Jul; 74(4):244-50. PubMed ID: 18454487
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Elevated levels of redox regulators, membrane-bound globin chains, and cytoskeletal protein fragments in hereditary spherocytosis erythrocyte proteome.
    Saha S; Ramanathan R; Basu A; Banerjee D; Chakrabarti A
    Eur J Haematol; 2011 Sep; 87(3):259-66. PubMed ID: 21575061
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.