BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

626 related articles for article (PubMed ID: 1726857)

  • 1. Molecular biology of hemoglobin: its application to sickle cell anemia and thalassemia.
    Kan YW
    Schweiz Med Wochenschr Suppl; 1991; 43():51-4. PubMed ID: 1726857
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Future prospects for treatment of hemoglobinopathies.
    Stamatoyannopoulos JA
    West J Med; 1992 Dec; 157(6):631-6. PubMed ID: 1282285
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach.
    Basak AN; Tuzmen S
    Methods Mol Biol; 2011; 700():291-307. PubMed ID: 21204041
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid detection of fetal Mendelian disorders: thalassemia and sickle cell syndromes.
    Traeger-Synodinos J; Vrettou C; Kanavakis E
    Methods Mol Biol; 2008; 444():133-45. PubMed ID: 18425477
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The intrauterine diagnosis of hemoglobin disorders.
    Wong SC; Ali MA; Benzie R
    Clin Perinatol; 1984 Jun; 11(2):283-308. PubMed ID: 6086205
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders.
    Perrine SP; Ginder GD; Faller DV; Dover GH; Ikuta T; Witkowska HE; Cai SP; Vichinsky EP; Olivieri NF
    N Engl J Med; 1993 Jan; 328(2):81-6. PubMed ID: 7677966
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Current trends in hemoglobin genetic diseases].
    Girot R
    Nouv Rev Fr Hematol (1978); 1991; 33(2):189-94. PubMed ID: 1766851
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of thalassemias and hemoglobinopathies.
    Seale TW; Rennert OM
    Ann Clin Lab Sci; 1980; 10(5):383-94. PubMed ID: 6252819
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The thalassemia syndromes: lessons from molecular medicines index case.
    Benz EJ
    Trans Am Clin Climatol Assoc; 1996; 107():20-36; discussion 35-6. PubMed ID: 8725557
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hemoglobin switching and its clinical implications.
    Blau CA; Stamatoyannopoulos G
    Curr Opin Hematol; 1994 Mar; 1(2):136-42. PubMed ID: 9371272
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia.
    Embury SH; Dozy AM; Miller J; Davis JR; Kleman KM; Preisler H; Vichinsky E; Lande WN; Lubin BH; Kan YW; Mentzer WC
    N Engl J Med; 1982 Feb; 306(5):270-4. PubMed ID: 6172710
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Globin gene expression in hereditary persistence of fetal haemoglobin and (delta beta) (0)-thalassaemia.
    Poncz M; Henthorn P; Stoeckert C; Surrey S
    Oxf Surv Eukaryot Genes; 1988; 5():163-203. PubMed ID: 2472152
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Beta-thalassemia and sickle cell disease in culture of early erythroid precursors: hemoglobin synthesis and ultrastructural study.
    Beuzard Y; Tulliez M; Testa U; Vainchenker W; Dubart A; Tsapis A; Galacteros F; Breton-Gorius J; Rosa J
    Blood Cells; 1981; 7(1):179-200. PubMed ID: 7187747
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
    Andersson BA; Wering ME; Luo HY; Basran RK; Steinberg MH; Smith HP; Chui DH
    Eur J Haematol; 2007 Jan; 78(1):82-5. PubMed ID: 17038017
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Sickle cell syndrome. Association between hemoglobin S and β thalassemia].
    Gasparini NP; Agriello EE; Zanella MJ; Iommi MP; Maradei J; Sandoval MJ
    Medicina (B Aires); 2016; 76(6):369-372. PubMed ID: 27959846
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia.
    Nagel RL; Steinberg MH
    Pediatr Pathol Mol Med; 2001; 20(2):123-36. PubMed ID: 12673837
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disorders of the synthesis of human fetal hemoglobin.
    Manca L; Masala B
    IUBMB Life; 2008 Feb; 60(2):94-111. PubMed ID: 18379999
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya.
    Keser I; Sanlioglu AD; Manguoglu E; Guzeloglu Kayisli O; Nal N; Sargin F; Yesilipek A; Simsek M; Mendilcioglu I; Canatan D; Luleci G
    Acta Haematol; 2004; 111(4):205-10. PubMed ID: 15153712
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of hemoglobin variants. Prenatal diagnosis on a fetus at risk of having the hemoglobin variants S and/or C in combination with beta-thalassemia.
    Blanke S
    Scand J Clin Lab Invest Suppl; 1989; 194():51-5. PubMed ID: 2772555
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sickle cell disease: a multigenic perspective of a single gene disorder.
    Kutlar A
    Hemoglobin; 2007; 31(2):209-24. PubMed ID: 17486504
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 32.