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Items: 1 to 20 of 121

1.

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. doi: 10.1002/ajh.24872. Epub 2017 Aug 17. Review.

PMID:
28736939
2.

Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.

Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, Luo HY, Chui DH, Farrell JJ, Al-Ali AK, Alsultan A.

Blood Cells Mol Dis. 2013 Jun;51(1):22-6. doi: 10.1016/j.bcmd.2012.12.005. Epub 2013 Mar 7.

3.

A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.

Vathipadiekal V, Farrell JJ, Wang S, Edward HL, Shappell H, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Simkin I, Farrer LA, Jiang Z, Luo HY, Huang S, Mostoslavsky G, Murphy GJ, Patra PK, Chui DH, Alsultan A, Al-Ali AK, Sebastiani P, Steinberg MH.

Am J Hematol. 2016 Nov;91(11):1118-1122. doi: 10.1002/ajh.24527. Epub 2016 Aug 22.

4.

Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.

Italia K, Jain D, Gattani S, Jijina F, Nadkarni A, Sawant P, Nair S, Mohanty D, Ghosh K, Colah R.

Blood Cells Mol Dis. 2009 Jan-Feb;42(1):25-31. doi: 10.1016/j.bcmd.2008.08.003. Epub 2008 Oct 26.

PMID:
18954999
5.

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.

Sebastiani P, Farrell JJ, Alsultan A, Wang S, Edward HL, Shappell H, Bae H, Milton JN, Baldwin CT, Al-Rubaish AM, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra PK, Farrer LA, Ngo D, Vathipadiekal V, Chui DH, Al-Ali AK, Steinberg MH.

Blood Cells Mol Dis. 2015 Mar;54(3):224-30. doi: 10.1016/j.bcmd.2015.01.001. Epub 2015 Jan 30.

6.

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. doi: 10.1016/j.cyto.2013.10.009. Epub 2013 Nov 27.

7.

Fetal hemoglobin in sickle cell anemia.

Akinsheye I, Alsultan A, Solovieff N, Ngo D, Baldwin CT, Sebastiani P, Chui DH, Steinberg MH.

Blood. 2011 Jul 7;118(1):19-27. doi: 10.1182/blood-2011-03-325258. Epub 2011 Apr 13. Review.

8.

Beta-globin gene cluster haplotypes in sickle cell patients from southwest Iran.

Rahimi Z, Karimi M, Haghshenass M, Merat A.

Am J Hematol. 2003 Nov;74(3):156-60.

9.

Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.

Alsultan A, Alabdulaali MK, Griffin PJ, Alsuliman AM, Ghabbour HA, Sebastiani P, Albuali WH, Al-Ali AK, Chui DH, Steinberg MH.

Br J Haematol. 2014 Feb;164(4):597-604. doi: 10.1111/bjh.12650. Epub 2013 Nov 13.

10.

A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease.

Pule GD, Mowla S, Novitzky N, Wiysonge CS, Wonkam A.

Expert Rev Hematol. 2015 Oct;8(5):669-79. doi: 10.1586/17474086.2015.1078235. Epub 2015 Sep 1. Review.

11.

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. doi: 10.1016/j.arcmed.2012.08.014. Epub 2012 Oct 19.

PMID:
23085440
12.

Concordant fetal hemoglobin response to hydroxyurea in siblings with sickle cell disease.

Steinberg MH, Voskaridou E, Kutlar A, Loukopoulos D, Koshy M, Ballas SK, Castro O, Barton F.

Am J Hematol. 2003 Feb;72(2):121-6.

13.

Genetic determinants of HbF in Saudi Arabian and African Benin haplotype sickle cell anemia.

Shaikho EM, Farrell JJ, Alsultan A, Sebastiani P, Steinberg MH.

Am J Hematol. 2017 Sep;92(9):E555-E557. doi: 10.1002/ajh.24822. Epub 2017 Jul 19. No abstract available.

14.

Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?

Bitoungui VJ, Pule GD, Hanchard N, Ngogang J, Wonkam A.

OMICS. 2015 Mar;19(3):171-9. doi: 10.1089/omi.2014.0134. Review.

15.

Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.

Vathipadiekal V, Alsultan A, Baltrusaitis K, Farrell JJ, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Suliman A, Patra PK, Milton JN, Farrer LA, Chui DH, Al-Ali AK, Sebastiani P, Steinberg MH.

Am J Hematol. 2016 Jun;91(6):E308-11. doi: 10.1002/ajh.24368. Epub 2016 Apr 28. No abstract available.

16.

Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia.

Alsultan A, Ngo D, Bae H, Sebastiani P, Baldwin CT, Melista E, Suliman AM, Albuali WH, Nasserullah Z, Luo HY, Chui DH, Steinberg MH, Al-Ali AK.

Am J Hematol. 2013 Jun;88(6):531-2. doi: 10.1002/ajh.23434. Epub 2013 May 2. No abstract available.

17.

Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease.

Liu L, Pertsemlidis A, Ding LH, Story MD, Steinberg MH, Sebastiani P, Hoppe C, Ballas SK, Pace BS.

Exp Biol Med (Maywood). 2016 Apr;241(7):706-18. doi: 10.1177/1535370216642047. Epub 2016 Mar 27.

18.

Determinants of fetal hemoglobin response to hydroxyurea.

Steinberg MH.

Semin Hematol. 1997 Jul;34(3 Suppl 3):8-14. Review.

PMID:
9317196
19.

Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia.

Shaikho EM, Habara AH, Alsultan A, Al-Rubaish AM, Al-Muhanna F, Naserullah Z, Alsuliman A, Qutub HO, Patra PK, Sebastiani P, Baltrusaitis K, Farrell JJ, Jiang Z, Luo HY, Chui DH, Al-Ali AK, Steinberg MH.

Blood Cells Mol Dis. 2016 Jul;59:49-51. doi: 10.1016/j.bcmd.2016.04.001. Epub 2016 Apr 13. No abstract available.

PMID:
27282567
20.

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 May-Jun;23(3):377-80. doi: 10.1002/ajhb.21148. Epub 2011 Mar 8.

PMID:
21387457

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