BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

277 related articles for article (PubMed ID: 447835)

  • 1. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.
    Adams JG; Boxer LA; Baehner RL; Forget BG; Tsistrakis GA; Steinberg MH
    J Clin Invest; 1979 May; 63(5):931-8. PubMed ID: 447835
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Low output hemoglobins which produce the phenotype of thalassemia.
    Adams JG; Steinberg MH
    Prog Clin Biol Res; 1981; 55():81-98. PubMed ID: 6895257
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Imbalance in alpha and beta globin synthesis associated with a hemoglobinopathy.
    Rieder RF; James GW
    J Clin Invest; 1974 Oct; 54(4):948-56. PubMed ID: 4430724
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Modification of hemoglobin H disease by sickle trait.
    Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.
    Wood WG; Stamatoyannopoulos G
    J Clin Invest; 1975 Mar; 55(3):567-78. PubMed ID: 1167870
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Abnormal red cell membrane proteolytic activity in severe heterozygous beta-thalassemia.
    Ballas SK; Burka ER; Gill FM
    J Lab Clin Med; 1982 Feb; 99(2):263-74. PubMed ID: 7038010
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MRNA analysis in reticulocytes of subjects with Hb D, Hb Porto Alegre, Hb E, and different types of unstable hemoglobin variants.
    Smetanina NS; Huisman TH
    Am J Hematol; 1996 Aug; 52(4):258-63. PubMed ID: 8701943
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).
    Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH
    J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Catabolism of hemoglobin by human erythrocyte membranes.
    Ballas SK; Burka ER
    J Lab Clin Med; 1978 Sep; 92(3):387-92. PubMed ID: 681824
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 86(4):363-7. PubMed ID: 11325640
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Analysis of a program for atypical familial microcytosis. Molecular basis of alpha-thalassemia].
    Villegas Martínez A
    Sangre (Barc); 1990 Aug; 35(4):277-88. PubMed ID: 2274839
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytes.
    Nienhuis AW; Anderson WF
    J Clin Invest; 1971 Nov; 50(11):2458-60. PubMed ID: 5096528
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel beta-globin structural mutant, Hb Brescia (beta 114 Leu-Pro), causing a severe beta-thalassemia intermedia phenotype.
    Murru S; Poddie D; Sciarratta GV; Agosti S; Baffico M; Melevendi C; Pirastu M; Cao A
    Hum Mutat; 1992; 1(2):124-8. PubMed ID: 1301199
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Silent thalassemias: genotypes and phenotypes.
    Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
    Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Hemoglobin O Arab in interaction with beta 0-thalassemia].
    Nikolov N; Andreeva M; Janković L; Efremov GD
    Lijec Vjesn; 1989; 111(1-2):27-30. PubMed ID: 2739498
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hemoglobin North Shore: a variant hemoglobin associated with the phenotype of beta-thalassemia.
    Smith CM; Hedlund B; Cich JA; Tukey DP; Olson M; Steinberg MH; Adams JG
    Blood; 1983 Feb; 61(2):378-83. PubMed ID: 6821704
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Post-transcriptional effects of interleukin-3, interferon-gamma, erythropoietin and butyrate on in vitro hemoglobin chain synthesis in congenital hemolytic anemia.
    Reinhardt D; Ridder R; Kugler W; Pekrun A
    Haematologica; 2001 Aug; 86(8):791-800. PubMed ID: 11522534
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular mechanisms of thalassemia in southeast Asia.
    Winichagoon P; Fucharoen S; Wilairat P; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():235-40. PubMed ID: 8629113
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.