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Items: 1 to 20 of 220

1.

Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia.

Wyszynski DF, Baldwin CT, Cleves MA, Amirault Y, Nolan VG, Farrell JJ, Bisbee A, Kutlar A, Farrer LA, Steinberg MH.

Cell Mol Biol (Noisy-le-grand). 2004 Feb;50(1):23-33.

PMID:
15040424
2.

Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations.

Sebastiani P, Wang L, Nolan VG, Melista E, Ma Q, Baldwin CT, Steinberg MH.

Am J Hematol. 2008 Mar;83(3):189-95.

3.

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.

Ma Q, Wyszynski DF, Farrell JJ, Kutlar A, Farrer LA, Baldwin CT, Steinberg MH.

Pharmacogenomics J. 2007 Dec;7(6):386-94. Epub 2007 Feb 13.

PMID:
17299377
4.

The HBS1L-MYB intergenic region on chromosome 6q23 is a quantitative trait locus controlling fetal haemoglobin level in carriers of beta-thalassaemia.

So CC, Song YQ, Tsang ST, Tang LF, Chan AY, Ma ES, Chan LC.

J Med Genet. 2008 Nov;45(11):745-51. doi: 10.1136/jmg.2008.060335. Epub 2008 Aug 12.

PMID:
18697826
5.

Genetic etiologies for phenotypic diversity in sickle cell anemia.

Steinberg MH.

ScientificWorldJournal. 2009 Jan 18;9:46-67. doi: 10.1100/tsw.2009.10. Review.

6.

Determinants of fetal hemoglobin response to hydroxyurea.

Steinberg MH.

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

PMID:
9317196
8.

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.

9.

Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.

Akinsheye I, Solovieff N, Ngo D, Malek A, Sebastiani P, Steinberg MH, Chui DH.

Am J Hematol. 2012 Feb;87(2):217-9. doi: 10.1002/ajh.22221. Epub 2011 Dec 3.

10.

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.

PMID:
15040425
11.

The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients.

Nguyen TK, Joly P, Bardel C, Moulsma M, Bonello-Palot N, Francina A.

Blood Cells Mol Dis. 2010 Aug 15;45(2):124-7. doi: 10.1016/j.bcmd.2010.04.002. Epub 2010 May 15.

PMID:
20472475
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.

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 8;254(1):181-7.

PMID:
9920754
14.

Discovering the genetics underlying foetal haemoglobin production in adults.

Thein SL, Menzel S.

Br J Haematol. 2009 May;145(4):455-67. doi: 10.1111/j.1365-2141.2009.07650.x. Epub 2008 Mar 2. Review.

PMID:
19344402
15.

DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.

Lettre G, Sankaran VG, Bezerra MA, Ara├║jo AS, Uda M, Sanna S, Cao A, Schlessinger D, Costa FF, Hirschhorn JN, Orkin SH.

Proc Natl Acad Sci U S A. 2008 Aug 19;105(33):11869-74. doi: 10.1073/pnas.0804799105. Epub 2008 Jul 30.

16.

The genetics of hemoglobin A2 regulation in sickle cell anemia.

Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH.

Am J Hematol. 2014 Nov;89(11):1019-23. doi: 10.1002/ajh.23811. Epub 2014 Aug 4.

17.

High fetal hemoglobin production in sickle cell anemia in the eastern province of Saudi Arabia is genetically determined.

Miller BA, Salameh M, Ahmed M, Wainscoat J, Antognetti G, Orkin S, Weatherall D, Nathan DG.

Blood. 1986 May;67(5):1404-10.

18.

Genetic variants associated with fetal hemoglobin levels show the diverse ethnic origin in Colombian patients with sickle cell anemia.

Fong C, Menzel S, Lizarralde MA, Barreto G.

Biomedica. 2015 Jul-Sep;35(3):437-43. doi: 10.7705/biomedica.v35i3.2573.

19.

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.

20.

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