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 *

200 related articles for article (PubMed ID: 18387321)

  • 21. Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis.
    Demiralp DO; Peker S; Turgut B; Akar N
    Proteomics Clin Appl; 2012 Aug; 6(7-8):403-11. PubMed ID: 22807418
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Relation between types of erythrocyte membrane defects and the clinical picture in hereditary spherocytosis].
    Brabec V; Palek J; Petrtýlová K; Cermák J; Jarolím P
    Vnitr Lek; 1997 Feb; 43(2):91-4. PubMed ID: 9245075
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 in hereditary spherocytosis (HS).
    Ayala S; Besson I; Aymerich M; Berga L; Vives Corrons JL
    Int J Hematol; 1995 Jul; 62(1):53-4. PubMed ID: 7670008
    [No Abstract]   [Full Text] [Related]  

  • 24. Complementary markers for the clinical severity classification of hereditary spherocytosis in unsplenectomized patients.
    Rocha S; Costa E; Rocha-Pereira P; Ferreira F; Cleto E; Barbot J; Quintanilha A; Belo L; Santos-Silva A
    Blood Cells Mol Dis; 2011 Feb; 46(2):166-70. PubMed ID: 21138793
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Polymorphism analysis of G199A, Ncol in ANK1 and Memphis I in SLC4A1 genes in Mexican healthy individuals and subjects affected with hereditary spherocytosis].
    Camacho-Torres AL; Sánchez-López JY; Mesa-Cornejo VM; Ibarra B; Perea-Díaz FJ
    Gac Med Mex; 2006; 142(5):435-7. PubMed ID: 17128827
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Interactions between peroxiredoxin 2, hemichrome and the erythrocyte membrane.
    Bayer SB; Low FM; Hampton MB; Winterbourn CC
    Free Radic Res; 2016 Dec; 50(12):1329-1339. PubMed ID: 27677384
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The effect of splenectomy in hereditary spherocytosis by dual angle laser light cytometry.
    Ricard MP; Gilsanz F
    Clin Lab Haematol; 1996 Dec; 18(4):249-51. PubMed ID: 9054697
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. [Erythrocyte indexes in hereditary spherocytosis].
    Eberle SE; Sciuccati G; Bonduel M; Díaz L; Staciuk R; Torres AF
    Medicina (B Aires); 2007; 67(6 Pt 2):698-700. PubMed ID: 18422060
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The diagnosis and management of hereditary spherocytosis.
    Bolton-Maggs PH
    Baillieres Best Pract Res Clin Haematol; 2000 Sep; 13(3):327-42. PubMed ID: 11030038
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Catalase, Glutathione Peroxidase, and Peroxiredoxin 2 in Erythrocyte Cytosol and Membrane in Hereditary Spherocytosis, Sickle Cell Disease, and β-Thalassemia.
    Melo D; Ferreira F; Teles MJ; Porto G; Coimbra S; Rocha S; Santos-Silva A
    Antioxidants (Basel); 2024 May; 13(6):. PubMed ID: 38929068
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Abnormal membrane protein of red blood cells in hereditary spherocytosis.
    Jacob HS; Ruby A; Overland ES; Mazia D
    J Clin Invest; 1971 Sep; 50(9):1800-5. PubMed ID: 5564386
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele.
    Miraglia del Giudice E; Francese M; Polito R; Nobili B; Iolascon A; Perrotta S
    Haematologica; 1997; 82(3):332-3. PubMed ID: 9234582
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hematologically important mutations: ankyrin variants in hereditary spherocytosis.
    Gallagher PG
    Blood Cells Mol Dis; 2005; 35(3):345-7. PubMed ID: 16223590
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. [Hereditary spherocytosis -- prevalence of erythrocyte membrane protein deficiency].
    Granjo E; Manata P; Torres N; Rodrigues L; Ferreira F; Bauerle R; Quintanilha A
    Acta Med Port; 2003; 16(2):65-9. PubMed ID: 12828006
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Propolis influence on erythrocyte membrane disorder (hereditary spherocytosis): a first approach.
    Moreira LL; Dias T; Dias LG; Rogão M; Da Silva JP; Estevinho LM
    Food Chem Toxicol; 2011 Feb; 49(2):520-6. PubMed ID: 21130830
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The novel role of peroxiredoxin-2 in red cell membrane protein homeostasis and senescence.
    Matté A; Pantaleo A; Ferru E; Turrini F; Bertoldi M; Lupo F; Siciliano A; Ho Zoon C; De Franceschi L
    Free Radic Biol Med; 2014 Nov; 76():80-8. PubMed ID: 25151118
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Heterozygosity of CDAN II (HEMPAS) gene may be detected by the analysis of erythrocyte membrane glycoconjugates from healthy carriers.
    Zdebska E; Mendek-Czajkowska E; Ploski R; Woêniewicz B; Koscielak J
    Haematologica; 2002 Feb; 87(2):126-30. PubMed ID: 11836161
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.