BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 2446459)

  • 1. A short review of human gamma-globin gene anomalies.
    Huisman TH
    Acta Haematol; 1987; 78(2-3):80-4. PubMed ID: 2446459
    [TBL] [Abstract][Full Text] [Related]  

  • 2. %Hb A2, %Hb F, %G gamma values and the haplotypes in the beta-globin gene cluster in Japanese adults with elevated Hb F.
    Shimizu K; Keino H
    Hum Hered; 1992; 42(4):222-30. PubMed ID: 1380945
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene.
    Stoming TA; Stoming GS; Lanclos KD; Fei YJ; Altay C; Kutlar F; Huisman TH
    Blood; 1989 Jan; 73(1):329-33. PubMed ID: 2462941
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Australian type of nondeletional G gamma-HPFH has a C-->G substitution at nucleotide -114 of the G gamma gene.
    Motum PI; Deng ZM; Huong L; Trent RJ
    Br J Haematol; 1994 Jan; 86(1):219-21. PubMed ID: 7516698
    [TBL] [Abstract][Full Text] [Related]  

  • 6. G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesis.
    Coleman MB; Adams JG; Steinberg MH; Plonczynski MW; Harrell AH; Castro O; Winter WP
    Am J Hematol; 1993 Feb; 42(2):186-90. PubMed ID: 7679879
    [TBL] [Abstract][Full Text] [Related]  

  • 7. G gamma-196 C-->T, A gamma-201 C-->T: two novel mutations in the promoter region of the gamma-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece.
    Tasiopoulou M; Boussiou M; Sinopoulou K; Moraitis G; Loutradi-Anagnostou A; Karababa P
    Blood Cells Mol Dis; 2008; 40(3):320-2. PubMed ID: 18096417
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Nondeletional type of hereditary persistence of fetal haemoglobin: molecular characterization of three unrelated Thai HPFH.
    Winichagoon P; Fucharoen S; Wilairat P; Chihara K; Fukumaki Y
    Br J Haematol; 1994 Aug; 87(4):797-804. PubMed ID: 7527242
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin.
    Collins FS; Metherall JE; Yamakawa M; Pan J; Weissman SM; Forget BG
    Nature; 1985 Jan 24-30; 313(6000):325-6. PubMed ID: 2578620
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH.
    Surrey S; Delgrosso K; Malladi P; Schwartz E
    Blood; 1988 Mar; 71(3):807-10. PubMed ID: 2449926
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFH.
    Gottardi E; Losekoot M; Fodde R; Saglio G; Camaschella C; Bernini LF
    Br J Haematol; 1992 Apr; 80(4):533-8. PubMed ID: 1374633
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variant.
    Farquhar M; Gelinas R; Tatsis B; Murray J; Yagi M; Mueller R; Stamatoyannopoulos G
    Am J Hum Genet; 1983 Jul; 35(4):611-20. PubMed ID: 6192712
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sardinian G gamma-HPFH: a T----C substitution in a conserved "octamer" sequence in the G gamma-globin promoter.
    Ottolenghi S; Nicolis S; Taramelli R; Malgaretti N; Mantovani R; Comi P; Giglioni B; Longinotti M; Dore F; Oggiano L
    Blood; 1988 Mar; 71(3):815-7. PubMed ID: 2449927
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel C-T transition within the distal CCAAT motif of the G gamma-globin gene in the Japanese HPFH: implication of factor binding in elevated fetal globin expression.
    Fucharoen S; Shimizu K; Fukumaki Y
    Nucleic Acids Res; 1990 Sep; 18(17):5245-53. PubMed ID: 1698280
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A fetal globin gene mutation in A gamma nondeletion hereditary persistence of fetal hemoglobin increases promoter strength in a nonerythroid cell.
    Rixon MW; Gelinas RE
    Mol Cell Biol; 1988 Feb; 8(2):713-21. PubMed ID: 2451123
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identical mutations in the paralogous human γ-globin genes leading to hemoglobin variants and nondeletional hereditary persistence of fetal hemoglobin.
    Papachatzopoulou A; Patrinos GP
    Hemoglobin; 2011; 35(2):135-41. PubMed ID: 21417570
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The deletion of the distal CCAAT box region of the A gamma-globin gene in black HPFH abolishes the binding of the erythroid specific protein NFE3 and of the CCAAT displacement protein.
    Mantovani R; Superti-Furga G; Gilman J; Ottolenghi S
    Nucleic Acids Res; 1989 Aug; 17(16):6681-91. PubMed ID: 2476717
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.