138 related articles for article (PubMed ID: 27274608)
1. Influence of βS-Globin Haplotypes and Hydroxyurea on Arginase I Levels in Sickle Cell Disease.
Moreira JA; Machado RP; Laurentino MR; Lemes RP; Barbosa MC; Santos TE; Bandeira IC; Martins AM
Dis Markers; 2016; 2016():9172726. PubMed ID: 27274608
[TBL] [Abstract][Full Text] [Related]
2. 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; 65(2):217-21. PubMed ID: 24290434
[TBL] [Abstract][Full Text] [Related]
3. Impact of β(S)-globin haplotypes on oxidative stress in patients with sickle cell anemia in steady state.
Carvalho-dos Santos BS; Dias-Elias DB; da Silva-Rocha LB; Cavalcante-Barbosa M; Pinheiro-Gonçalves R
Arch Med Res; 2012 Oct; 43(7):536-40. PubMed ID: 23085440
[TBL] [Abstract][Full Text] [Related]
4. Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea.
Bernaudin F; Arnaud C; Kamdem A; Hau I; Lelong F; Epaud R; Pondarré C; Pissard S
Blood Adv; 2018 Mar; 2(6):626-637. PubMed ID: 29555644
[TBL] [Abstract][Full Text] [Related]
5. 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; 23(6):815-9. PubMed ID: 21965081
[TBL] [Abstract][Full Text] [Related]
6. β
Abou-Elew HH; Youssry I; Hefny S; Hashem RH; Fouad N; Zayed RA
Hematology; 2018 Jul; 23(6):362-367. PubMed ID: 29157167
[TBL] [Abstract][Full Text] [Related]
7. Inheritance of the Bantu/Benin haplotype causes less severe hemolytic and oxidative stress in sickle cell anemia patients treated with hydroxycarbamide.
Okumura JV; Silva DG; Torres LS; Belini-Junior E; Barberino WM; Oliveira RG; Carrocini GC; Gelaleti GB; Lobo CL; Bonini-Domingos CR
J Hum Genet; 2016 Jul; 61(7):605-11. PubMed ID: 26961071
[TBL] [Abstract][Full Text] [Related]
8. Influence of βS-globin haplotypes and hydroxyurea on tumor necrosis factor-alpha levels in sickle cell anemia.
Laurentino MR; Maia PA; Barbosa MC; Bandeira IC; Rocha LB; Gonçalves RP
Rev Bras Hematol Hemoter; 2014 Mar; 36(2):121-5. PubMed ID: 24790537
[TBL] [Abstract][Full Text] [Related]
9. 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; 23(3):377-80. PubMed ID: 21387457
[TBL] [Abstract][Full Text] [Related]
10. Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia.
Silva DG; Belini Junior E; Carrocini GC; Torres Lde S; Ricci Júnior O; Lobo CL; Bonini-Domingos CR; de Almeida EA
BMC Med Genet; 2013 Oct; 14():108. PubMed ID: 24106994
[TBL] [Abstract][Full Text] [Related]
11. DNA damage in leukocytes of sickle cell anemia patients is associated with hydroxyurea therapy and with HBB*S haplotype.
da Silva Rocha LB; Dias Elias DB; Barbosa MC; Bandeira IC; Gonçalves RP
Mutat Res; 2012 Dec; 749(1-2):48-52. PubMed ID: 22918118
[TBL] [Abstract][Full Text] [Related]
12. Atypical beta(s) haplotypes are generated by diverse genetic mechanisms.
Zago MA; Silva WA; Dalle B; Gualandro S; Hutz MH; Lapoumeroulie C; Tavella MH; Araujo AG; Krieger JE; Elion J; Krishnamoorthy R
Am J Hematol; 2000 Feb; 63(2):79-84. PubMed ID: 10629573
[TBL] [Abstract][Full Text] [Related]
13. Hydroxyurea improves nitric oxide bioavailability in humanized sickle cell mice.
Taylor CM; Kasztan M; Sedaka R; Molina PA; Dunaway LS; Pollock JS; Pollock DM
Am J Physiol Regul Integr Comp Physiol; 2021 May; 320(5):R630-R640. PubMed ID: 33624556
[TBL] [Abstract][Full Text] [Related]
14. Beta-globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in Lebanon.
Inati A; Taher A; Bou Alawi W; Koussa S; Kaspar H; Shbaklo H; Zalloua PA
Eur J Haematol; 2003 Feb; 70(2):79-83. PubMed ID: 12581188
[TBL] [Abstract][Full Text] [Related]
15. High-density SNP genotyping to define beta-globin locus haplotypes.
Liu L; Muralidhar S; Singh M; Sylvan C; Kalra IS; Quinn CT; Onyekwere OC; Pace BS
Blood Cells Mol Dis; 2009; 42(1):16-24. PubMed ID: 18829352
[TBL] [Abstract][Full Text] [Related]
16. Frequency of beta S globin gene haplotypes among sickle cell patients in Nigeria.
Adabale A; Makanjuola SBL; Akinbami A; Dosunmu A; Akanmu A; Javid FA; Ajonuma LC
J Int Med Res; 2021 Jun; 49(6):3000605211019918. PubMed ID: 34187213
[TBL] [Abstract][Full Text] [Related]
17. 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; 34(3):262-6. PubMed ID: 22260316
[TBL] [Abstract][Full Text] [Related]
18. Rapid and reliable β-globin gene cluster haplotyping of sickle cell disease patients by FRET Light Cycler and HRM assays.
Joly P; Lacan P; Garcia C; Delasaux A; Francina A
Clin Chim Acta; 2011 Jun; 412(13-14):1257-61. PubMed ID: 21440534
[TBL] [Abstract][Full Text] [Related]
19. Identification of β-globin haplotypes linked to sickle hemoglobin (Hb S) alleles in Mazandaran province, Iran.
Aghajani F; Mahdavi MR; Kosaryan M; Mahdavi M; Hamidi M; Jalali H
Genes Genet Syst; 2017 May; 91(6):311-313. PubMed ID: 28003571
[TBL] [Abstract][Full Text] [Related]
20. Fetal hemoglobin in sickle cell anemia: The Arab-Indian haplotype and new therapeutic agents.
Habara AH; Shaikho EM; Steinberg MH
Am J Hematol; 2017 Nov; 92(11):1233-1242. PubMed ID: 28736939
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
