BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

284 related articles for article (PubMed ID: 1704267)

  • 1. Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.
    Losekoot M; Fodde R; Gerritsen EJ; van de Kuit I; Schreuder A; Giordano PC; Vossen JM; Bernini LF
    Blood; 1991 Feb; 77(4):861-7. PubMed ID: 1704267
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?
    Ottolenghi S; Giglioni B; Taramelli R; Comi P; Mazza U; Saglio G; Camaschella C; Izzo P; Cao A; Galanello R; Gimferrer E; Baiget M; Gianni AM
    Proc Natl Acad Sci U S A; 1982 Apr; 79(7):2347-51. PubMed ID: 6179097
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal gamma-gene expression in association with beta thalassemia and linkage relationship with the beta-globin gene cluster.
    Giampaolo A; Mavilio F; Sposi NM; Carè A; Massa A; Cianetti L; Petrini M; Russo R; Cappellini MD; Marinucci M
    Hum Genet; 1984; 66(2-3):151-6. PubMed ID: 6201431
    [TBL] [Abstract][Full Text] [Related]  

  • 4. beta Thalassemia associated with increased HB F production. Evidence for the existence of a heterocellular hereditary persistence of fetal hemoglobin (HPFH) determinant linked to beta thalassemia in a southern Italian population.
    Marinucci M; Mavilio F; Giuliani A; Gabbianelli M; Tentori L; Tentori L; Zorini CO; Lamberti E; Palazzolo A; Lanzo D
    Hemoglobin; 1981; 5(1):1-17. PubMed ID: 6162827
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia.
    Clegg JB; Metaxatou-Mavromati A; Kattamis C; Sofroniadou K; Wood WG; Weatherall DJ
    Br J Haematol; 1979 Dec; 43(4):521-36. PubMed ID: 93488
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Delta beta thalassemia and hereditary persistence of fetal hemoglobin.
    Bollekens JA; Forget BG
    Hematol Oncol Clin North Am; 1991 Jun; 5(3):399-422. PubMed ID: 1713909
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The gamma chain heterogeneity of fetal hemoglobin in black beta-thalassemia and HPFH heterozygotes.
    Huisman TH; Gravely ME; Webber B; Okonjo K; Henson J; Reese AL
    Blood; 1981 Jul; 58(1):62-70. PubMed ID: 6165415
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex.
    Thein SL; Weatherall DJ
    Prog Clin Biol Res; 1989; 316B():97-111. PubMed ID: 2482508
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemia.
    Ottolenghi S; Camaschella C; Comi P; Giglioni B; Longinotti M; Oggiano L; Dore F; Sciarratta G; Ivaldi G; Saglio G
    Hum Genet; 1988 May; 79(1):13-7. PubMed ID: 2452784
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary persistence of fetal hemoglobin or (delta beta)o-thalassemia: three types observed in South-Chinese families.
    Zeng YT; Huang SZ; Chen B; Liang YC; Chang ZM; Harano T; Huisman TH
    Blood; 1985 Dec; 66(6):1430-5. PubMed ID: 2415188
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular characterization of hereditary persistence of fetal hemoglobin in the Karen people of Thailand.
    Trachoo O; Sura T; Sakuntabhai A; Singhasivanon P; Krudsood S; Phimpraphi W; Krasaesub S; Chanjarunee S; Looareesuwan S
    Hemoglobin; 2003 May; 27(2):97-104. PubMed ID: 12779271
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster.
    Feingold EA; Forget BG
    Blood; 1989 Nov; 74(6):2178-86. PubMed ID: 2478223
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Greek (A gamma) variant of hereditary persistence of fetal haemoglobin: globin gene organization and studies of expression of fetal haemoglobins in clonal erythroid cultures.
    Papayannopoulou T; Lawn RM; Stamatoyannopoulos G; Maniatis T
    Br J Haematol; 1982 Mar; 50(3):387-99. PubMed ID: 6175332
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.
    Indrak K; Indrakova J; Kutlar F; Pospisilova D; Sulovska I; Baysal E; Huisman TH
    Ann Hematol; 1991 Aug; 63(2):111-5. PubMed ID: 1716997
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia.
    Wood WG; Clegg JB; Weatherall DJ
    Br J Haematol; 1979 Dec; 43(4):509-20. PubMed ID: 93487
    [No Abstract]   [Full Text] [Related]  

  • 16. Globin mRNA in beta-thalassemia heterozygotes with different beta-thalassemia alleles and in heterozygotes for hereditary persistence of fetal hemoglobin.
    Smetanina NS; Adekile AD; Huisman TH
    Acta Haematol; 1996; 96(3):162-9. PubMed ID: 8876614
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Physical mapping of the globin gene deletion in hereditary persistence of foetal haemoglobin (HPFH).
    Bernards R; Flavell RA
    Nucleic Acids Res; 1980 Apr; 8(7):1521-34. PubMed ID: 6159595
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification.
    Craig JE; Barnetson RA; Prior J; Raven JL; Thein SL
    Blood; 1994 Mar; 83(6):1673-82. PubMed ID: 7510147
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.
    Cianetti L; Care A; Sposi NM; Giampaolo A; Calandrini M; Petrini M; Massa A; Marinucci M; Mavilio F; Ceccanti M
    J Med Genet; 1984 Aug; 21(4):263-7. PubMed ID: 6208362
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newborn.
    Huisman TH; Efremov GD; Reese AL; Howard JS; Gravely ME; Harris HF; Wilson JB
    Hemoglobin; 1979; 3(4):223-52. PubMed ID: 500369
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.