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Journal Abstract Search

672 related items for PubMed ID: 14587041

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  • 3. DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC disease.
    Konstantopoulos K, Vulliamy T, Swirsky D, Reeves JD, Kaeda J, Luzzatto L.
    Gene Geogr; 1996 Apr; 10(1):19-24. PubMed ID: 8913718
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  • 4. 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
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  • 5. Molecular characteristics of pediatric patients with sickle cell anemia and stroke.
    Sarnaik SA, Ballas SK.
    Am J Hematol; 2001 Jul; 67(3):179-82. PubMed ID: 11391715
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  • 6. Localisation of cis regulatory elements at the beta-globin locus: analysis of hybrid haplotype chromosomes.
    Ofori-Acquah SF, Lalloz MR, Layton DM.
    Biochem Biophys Res Commun; 1999 Jan 08; 254(1):181-7. PubMed ID: 9920754
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  • 7. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA, Jalal SD, Nerwey FF, Al-Sayan GO, Al-Zebari SS, Alshingaly AA, Markous RD, Jubrael JM, Hamamy H.
    Hemoglobin; 2012 Jan 08; 36(4):333-42. PubMed ID: 22686351
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  • 10. Chronic inflammatory state in sickle cell anemia patients is associated with HBB(*)S haplotype.
    Bandeira IC, Rocha LB, Barbosa MC, Elias DB, Querioz JA, Freitas MV, Gonçalves RP.
    Cytokine; 2014 Feb 08; 65(2):217-21. PubMed ID: 24290434
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  • 13. Restriction mapping of βS locus among Tunisian sickle-cell patients.
    Imen M, Ikbel BM, Leila C, Fethi M, Amine Z, Mohamed B, Salem A.
    Am J Hum Biol; 2011 Feb 08; 23(6):815-9. PubMed ID: 21965081
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  • 14. Molecular analysis of the β-globin gene cluster haplotypes in a Sudanese population with sickle cell anaemia.
    Elderdery AY, Mills J, Mohamed BA, Cooper AJ, Mohammed AO, Eltieb N, Old J.
    Int J Lab Hematol; 2012 Jun 08; 34(3):262-6. PubMed ID: 22260316
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  • 15. β-globin gene cluster haplotypes in sickle cell patients from Panamá.
    Rusanova I, Cossio G, Moreno B, Javier Perea F, De Borace RG, Perea M, Escames G, Acuña-Castroviejo D.
    Am J Hum Biol; 2011 Jun 08; 23(3):377-80. PubMed ID: 21387457
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  • 16. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
    Adekile A, Kutlar F, McKie K, Addington A, Elam D, Holley L, Clair B, Kutlar A.
    Eur J Haematol; 2005 Aug 08; 75(2):150-5. PubMed ID: 16004608
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  • 17. Haplotypes in tribal Indians bearing the sickle gene: evidence for the unicentric origin of the beta S mutation and the unicentric origin of the tribal populations of India.
    Labie D, Srinivas R, Dunda O, Dode C, Lapoumeroulie C, Devi V, Devi S, Ramasami K, Elion J, Ducrocq R.
    Hum Biol; 1989 Aug 08; 61(4):479-91. PubMed ID: 2480325
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  • 19. Raised Hb F levels in sickle cell disease are caused by a determinant linked to the beta globin gene cluster.
    Kulozik AE, Thein SL, Kar BC, Wainscoat JS, Serjeant GR, Weatherall DJ.
    Prog Clin Biol Res; 1987 Aug 08; 251():427-39. PubMed ID: 2448811
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  • 20. Haplotype analysis of beta thalassemia patients in Western Iran.
    Rahimi Z, Muniz A, Akramipour R, Tofieghzadeh F, Mozafari H, Vaisi-Raygani A, Parsian A.
    Blood Cells Mol Dis; 2009 Aug 08; 42(2):140-3. PubMed ID: 19141369
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