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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (PubMed ID: 1699206)

  • 1. The T----C substitution at -198 of the A gamma-globin gene associated with the British form of HPFH generates overlapping recognition sites for two DNA-binding proteins.
    Fischer KD; Nowock J
    Nucleic Acids Res; 1990 Oct; 18(19):5685-93. PubMed ID: 1699206
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Methylation-enhanced binding of Sp1 to the stage selector element of the human gamma-globin gene promoter may regulate development specificity of expression.
    Jane SM; Gumucio DL; Ney PA; Cunningham JM; Nienhuis AW
    Mol Cell Biol; 1993 Jun; 13(6):3272-81. PubMed ID: 7684493
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Increased gamma-globin expression in a nondeletion HPFH mediated by an erythroid-specific DNA-binding factor.
    Martin DI; Tsai SF; Orkin SH
    Nature; 1989 Mar; 338(6214):435-8. PubMed ID: 2467208
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA sequences regulating human globin gene transcription in nondeletional hereditary persistence of fetal hemoglobin.
    Ottolenghi S; Mantovani R; Nicolis S; Ronchi A; Giglioni B
    Hemoglobin; 1989; 13(6):523-41. PubMed ID: 2481658
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased Sp1 binding mediates erythroid-specific overexpression of a mutated (HPFH) gamma-globulin promoter.
    Ronchi A; Nicolis S; Santoro C; Ottolenghi S
    Nucleic Acids Res; 1989 Dec; 17(24):10231-41. PubMed ID: 2481268
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The effects of HPFH mutations in the human gamma-globin promoter on binding of ubiquitous and erythroid specific nuclear factors.
    Mantovani R; Malgaretti N; Nicolis S; Ronchi A; Giglioni B; Ottolenghi S
    Nucleic Acids Res; 1988 Aug; 16(16):7783-97. PubMed ID: 2458563
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comparative studies of nondeletional HPFH gamma-globin gene promoters.
    Motum PI; Lindeman R; Harvey MP; Trent RJ
    Exp Hematol; 1993 Jul; 21(7):852-8. PubMed ID: 7686501
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Nuclear proteins that bind the human gamma-globin gene promoter: alterations in binding produced by point mutations associated with hereditary persistence of fetal hemoglobin.
    Gumucio DL; Rood KL; Gray TA; Riordan MF; Sartor CI; Collins FS
    Mol Cell Biol; 1988 Dec; 8(12):5310-22. PubMed ID: 2468996
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A naturally occurring gamma globin gene mutation enhances SP1 binding activity.
    Sykes K; Kaufman R
    Mol Cell Biol; 1990 Jan; 10(1):95-102. PubMed ID: 1688466
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Molecular analysis of the human fetal-to-adult globin switching.
    Katsube T; Fucharoen S; Tojo H; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():212-20. PubMed ID: 8629109
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of the mechanism of action of the Brazilian type (Agamma-195 C --> G) of hereditary persistence of fetal hemoglobin.
    Takahashi T; Schreiber R; Krieger JE; Saad ST; Costa FF
    Eur J Haematol; 2003 Dec; 71(6):418-24. PubMed ID: 14703691
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Purification and identification of proteins that bind to the hereditary persistence of fetal hemoglobin -198 mutation in the gamma-globin gene promoter.
    Olave IA; Doneanu C; Fang X; Stamatoyannopoulos G; Li Q
    J Biol Chem; 2007 Jan; 282(2):853-62. PubMed ID: 17114178
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sites I and II upstream of the A gamma globin gene bind nuclear factors and affect gene expression.
    Lloyd JA; Lee RF; Menon AG; Lingrel JB
    Prog Clin Biol Res; 1989; 316A():139-48. PubMed ID: 2480607
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in two regions upstream of the A gamma globin gene canonical promoter affect gene expression.
    Lloyd JA; Lee RF; Lingrel JB
    Nucleic Acids Res; 1989 Jun; 17(11):4339-52. PubMed ID: 2472607
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An A gamma globin promoter (four base-pair deletion) mutant shows linked polymorphic changes throughout the A gamma gene.
    Harvey MP; Motum P; Lindeman R; Trent RJ
    Exp Hematol; 1992 Mar; 20(3):320-3. PubMed ID: 1373683
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. HMG-I binds to GATA motifs: implications for an HPFH syndrome.
    Magis W; Martin DI
    Biochem Biophys Res Commun; 1995 Sep; 214(3):927-33. PubMed ID: 7575565
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.