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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

86 related items for PubMed ID: 8571932

  • 1. Two mutations in the locus control region hypersensitivity site-2 (5' HS-2) of haplotype 19 beta s chromosomes alter binding of trans-acting factors.
    Morgan JC, Scott DF, Lanclos KD.
    Am J Hematol; 1996 Jan; 51(1):12-8. PubMed ID: 8571932
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease.
    Ofori-Acquah SF, Lalloz MR, Serjeant G, Layton DM.
    Cell Mol Biol (Noisy-le-grand); 2004 Feb; 50(1):35-42. PubMed ID: 15040425
    [Abstract] [Full Text] [Related]

  • 6. Rearrangements of the beta-globin gene cluster in apparently typical betaS haplotypes.
    Zago MA, Silva WA, Gualandro S, Yokomizu IK, Araujo AG, Tavela MH, Gerard N, Krishnamoorthy R, Elion J.
    Haematologica; 2001 Feb; 86(2):142-5. PubMed ID: 11224482
    [Abstract] [Full Text] [Related]

  • 7. Transcriptional regulation of the hepatocyte growth factor (HGF) gene by the Sp family of transcription factors.
    Jiang JG, Chen Q, Bell A, Zarnegar R.
    Oncogene; 1997 Jun 26; 14(25):3039-49. PubMed ID: 9223667
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Molecular characteristics of pediatric patients with sickle cell anemia and stroke.
    Sarnaik SA, Ballas SK.
    Am J Hematol; 2001 Jul 26; 67(3):179-82. PubMed ID: 11391715
    [Abstract] [Full Text] [Related]

  • 10. Microsatellite and single nucleotide polymorphisms in the β-globin locus control region-hypersensitive Site 2: SPECIFICITY of Tunisian βs chromosomes.
    Ben Mustapha M, Moumni I, Zorai A, Douzi K, Ghanem A, Abbes S.
    Hemoglobin; 2012 Jul 26; 36(6):533-44. PubMed ID: 23101664
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia.
    Papachatzopoulou A, Kourakli A, Makropoulou P, Kakagianne T, Sgourou A, Papadakis M, Athanassiadou A.
    Eur J Haematol; 2006 Apr 26; 76(4):322-30. PubMed ID: 16519704
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. DNAase I hypersensitive site 3' to the beta-globin gene cluster contains a TAA insertion specific for beta(S)-Benin haplotype.
    Bordin S, Crespi VG, Duarte AS, Bassères DS, Melo MB, Vieira AP, Saad ST, Costa FF.
    Haematologica; 2002 Mar 26; 87(3):246-9. PubMed ID: 11869935
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. The proximal promoter of the human cathepsin G gene conferring myeloid-specific expression includes C/EBP, c-myb and PU.1 binding sites.
    Lennartsson A, Garwicz D, Lindmark A, Gullberg U.
    Gene; 2005 Aug 15; 356():193-202. PubMed ID: 16019164
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.