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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

257 related items for PubMed ID: 21264907

  • 21. Thalassemia: pathophysiology of red cell changes.
    Schrier SL.
    Annu Rev Med; 1994; 45():211-8. PubMed ID: 8198378
    [Abstract] [Full Text] [Related]

  • 22. Differential regulation of redox proteins and chaperones in HbEβ-thalassemia erythrocyte proteome.
    Bhattacharya D, Saha S, Basu S, Chakravarty S, Chakravarty A, Banerjee D, Chakrabarti A.
    Proteomics Clin Appl; 2010 May; 4(5):480-8. PubMed ID: 21137065
    [Abstract] [Full Text] [Related]

  • 23. Red cell parameters in alpha-thalassemia with and without beta-thalassemia trait or hemoglobin E trait.
    Jindadamrongwech S, Wisedpanichkij R, Bunyaratvej A, Hathirat P.
    Southeast Asian J Trop Med Public Health; 1997 May; 28 Suppl 3():97-9. PubMed ID: 9640607
    [Abstract] [Full Text] [Related]

  • 24. Interaction between endothelial cells and thalassemic red cells in vitro.
    Butthep P, Bunyaratvej A, Kitaguchi H, Funahara Y, Fucharoen S.
    Southeast Asian J Trop Med Public Health; 1992 May; 23 Suppl 2():101-4. PubMed ID: 1298981
    [Abstract] [Full Text] [Related]

  • 25. Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.
    Bunyaratvej A, Fucharoen S, Tatsumi N.
    Southeast Asian J Trop Med Public Health; 1992 May; 23 Suppl 2():86-90. PubMed ID: 1299000
    [Abstract] [Full Text] [Related]

  • 26. Erythroid bone marrow activity and red cell hemoglobinization in iron sufficient beta-thalassemia heterozygotes as reflected by soluble transferrin receptor and reticulocyte hemoglobin in content. Correlation with genotypes and Hb A(2) levels.
    Skarmoutsou C, Papassotiriou I, Traeger-Synodinos J, Stamou H, Ladis V, Metaxotou-Mavrommati A, Stamoulakatou A, Kanavakis E.
    Haematologica; 2003 Jun; 88(6):631-6. PubMed ID: 12801838
    [Abstract] [Full Text] [Related]

  • 27. Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography.
    Wan JH, Tian PL, Luo WH, Wu BY, Xiong F, Zhou WJ, Wei XC, Xu XM.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2012 Jul 15; 901():53-8. PubMed ID: 22727753
    [Abstract] [Full Text] [Related]

  • 28. An erythroid chaperone that facilitates folding of alpha-globin subunits for hemoglobin synthesis.
    Yu X, Kong Y, Dore LC, Abdulmalik O, Katein AM, Zhou S, Choi JK, Gell D, Mackay JP, Gow AJ, Weiss MJ.
    J Clin Invest; 2007 Jul 15; 117(7):1856-65. PubMed ID: 17607360
    [Abstract] [Full Text] [Related]

  • 29. Development of severe anemia during fever episodes in patients with hemoglobin E trait and hemoglobin H disease combinations.
    Jetsrisuparb A, Sanchaisuriya K, Fucharoen G, Fucharoen S, Wiangnon S, Jetsrisuparb C, Sirijirachai J, Chansoong K.
    J Pediatr Hematol Oncol; 2006 Apr 15; 28(4):249-53. PubMed ID: 16679924
    [Abstract] [Full Text] [Related]

  • 30. Red blood cell phenotypes in alpha-thalassemias in the Spanish population.
    Villegas A, Porres A, Sánchez J, González FA, Pérez-Clausell C, Martínez M, Murga MJ, Cachá J, Lozano M, Fernández-Fuertes I, Del Arco A, Arrizabalaga B, Pérez de Mendiguren B, San Juan I, Saavedra R, Ricart P, Sainz C, Guerra JL, Muñoz JA, Lago C, Ansó VM.
    Haematologica; 1998 Feb 15; 83(2):99-103. PubMed ID: 9580456
    [Abstract] [Full Text] [Related]

  • 31. AHSP and beta-thalassemia: a possible genetic modifier.
    dos Santos CO, Costa FF.
    Hematology; 2005 Apr 15; 10(2):157-61. PubMed ID: 16019463
    [Abstract] [Full Text] [Related]

  • 32. Association of alpha hemoglobin-stabilizing protein (AHSP) gene mutation and disease severity among HbE-beta thalassemia patients.
    Ray R, Kalantri SA, Bhattacharjee S, Biswas A, Shahab A, Biswas S, Bhattacharyya M.
    Ann Hematol; 2019 Aug 15; 98(8):1827-1834. PubMed ID: 31190133
    [Abstract] [Full Text] [Related]

  • 33. Hydration of red cells in alpha and beta thalassemias differs. A useful approach to distinguish between these red cell phenotypes.
    Bunyaratvej A, Fucharoen S, Greenbaum A, Mohandas N.
    Am J Clin Pathol; 1994 Aug 15; 102(2):217-22. PubMed ID: 8042592
    [Abstract] [Full Text] [Related]

  • 34. Implication of globin gene expression, hemoglobin F and hemoglobin E levels on β-thalassemia/Hb E disease severity.
    Siriworadechkul S, Jindadamrongwech S, Chuncharunee S, Aupparakkitanon S.
    Ann Clin Lab Sci; 2014 Aug 15; 44(4):437-42. PubMed ID: 25361929
    [Abstract] [Full Text] [Related]

  • 35. Study of alpha hemoglobin stabilizing protein expression in patients with β thalassemia and sickle cell anemia and its impact on clinical severity.
    Mahmoud HM, Shoeib AA, Abd El Ghany SM, Reda MM, Ragab IA.
    Blood Cells Mol Dis; 2015 Dec 15; 55(4):358-62. PubMed ID: 26460260
    [Abstract] [Full Text] [Related]

  • 36. Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene.
    Traeger-Synodinos J, Papassotiriou I, Vrettou C, Skarmoutsou C, Stamoulakatou A, Kanavakis E.
    Haematologica; 2001 Apr 15; 86(4):363-7. PubMed ID: 11325640
    [Abstract] [Full Text] [Related]

  • 37. Oxidative instability of hemoglobin E (β26 Glu→Lys) is increased in the presence of free α subunits and reversed by α-hemoglobin stabilizing protein (AHSP): Relevance to HbE/β-thalassemia.
    Strader MB, Kassa T, Meng F, Wood FB, Hirsch RE, Friedman JM, Alayash AI.
    Redox Biol; 2016 Aug 15; 8():363-74. PubMed ID: 26995402
    [Abstract] [Full Text] [Related]

  • 38. [Role of alpha-hemoglobin molecular chaperone in the hemoglobin formation and clinical expression of some hemoglobinopathies].
    Vasseur C, Baudin-Creuza V.
    Transfus Clin Biol; 2015 Mar 15; 22(1):49-57. PubMed ID: 25724329
    [Abstract] [Full Text] [Related]

  • 39. Alpha-hemoglobin-stabilizing protein (AHSP): a modulatory factor in β-thalassemia.
    Che Yaacob NS, Islam MA, Alsaleh H, Ibrahim IK, Hassan R.
    Int J Hematol; 2020 Mar 15; 111(3):352-359. PubMed ID: 31894534
    [Abstract] [Full Text] [Related]

  • 40. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Eur J Haematol; 2009 Jul 15; 83(1):57-65. PubMed ID: 19226360
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.