BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 10335983)

  • 1. A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin.
    Zertal-Zidani S; Merghoub T; Ducrocq R; Gerard N; Satta D; Krishnamoorthy R
    Hemoglobin; 1999 May; 23(2):159-69. PubMed ID: 10335983
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
    Hariharan P; Sawant M; Gorivale M; Manchanda R; Colah R; Ghosh K; Nadkarni A
    Mol Biol Rep; 2017 Oct; 44(5):413-417. PubMed ID: 28879539
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A role for the distal CCAAT box of the gamma-globin gene in Hb switching.
    Katsube T; Fukumaki Y
    J Biochem; 1995 Jan; 117(1):68-76. PubMed ID: 7539789
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Fetal hemoglobin expression in the compound heterozygous state for -117 (G-->A) Agamma HPFH and IVSII-745 (C-->G) beta+ thalassemia: a case study.
    Dedoussis GV; Sinopoulou K; Gyparaki M; Loutradis A
    Am J Hematol; 1999 Jun; 61(2):139-43. PubMed ID: 10367795
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
    Akinbami AO; Campbell AD; Han ZJ; Luo HY; Chui DH; Steinberg MH
    Hemoglobin; 2016; 40(1):64-5. PubMed ID: 26372199
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.
    Amato A; Cappabianca MP; Perri M; Zaghis I; Grisanti P; Ponzini D; Di Biagio P
    Int J Lab Hematol; 2014 Feb; 36(1):13-9. PubMed ID: 23621512
    [TBL] [Abstract][Full Text] [Related]  

  • 9. G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.
    Collins FS; Stoeckert CJ; Serjeant GR; Forget BG; Weissman SM
    Proc Natl Acad Sci U S A; 1984 Aug; 81(15):4894-8. PubMed ID: 6205403
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 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. Genetic heterogeneity in heterocellular hereditary persistence of fetal hemoglobin.
    Craig JE; Rochette J; Sampietro M; Wilkie AO; Barnetson R; Hatton CS; Demenais F; Thein SL
    Blood; 1997 Jul; 90(1):428-34. PubMed ID: 9207480
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the beta globin gene complex.
    Donald JA; Lammi A; Trent RJ
    Hum Genet; 1988 Sep; 80(1):69-74. PubMed ID: 2458313
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ggamma -37 (A-->T): a new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) delta0-thalassemia.
    Bouva MJ; Harteveld CL; Bakker-Verweij G; van Delft P; Giordano PC
    Hemoglobin; 2006; 30(3):371-7. PubMed ID: 16840228
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin.
    Arcasoy MO; Romana M; Fabry ME; Skarpidi E; Nagel RL; Forget BG
    Mol Cell Biol; 1997 Apr; 17(4):2076-89. PubMed ID: 9121456
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Original Research: Generation of non-deletional hereditary persistence of fetal hemoglobin β-globin locus yeast artificial chromosome transgenic mouse models: -175 Black HPFH and -195 Brazilian HPFH.
    Braghini CA; Costa FC; Fedosyuk H; Neades RY; Novikova LV; Parker MP; Winefield RD; Peterson KR
    Exp Biol Med (Maywood); 2016 Apr; 241(7):697-705. PubMed ID: 26946532
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.