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Items: 1 to 20 of 105

1.

Genetic modulation of HbF in Brazilians with HbSC disease and sickle cell anemia.

Barbosa CG, Aleluia AC, Pacheco AP, Paz SS, Zanette AM, Lyra IM, Steinberg MH, Milton JN, Goncalves MS.

Am J Hematol. 2013 Oct;88(10):923-4. doi: 10.1002/ajh.23538. Epub 2013 Sep 3. No abstract available.

2.

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.

3.

Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans.

Alsultan A, Solovieff N, Aleem A, AlGahtani FH, Al-Shehri A, Osman ME, Kurban K, Bahakim H, Al-Momen AK, Baldwin CT, Chui DH, Steinberg MH.

Am J Hematol. 2011 Jul;86(7):612-4. doi: 10.1002/ajh.22032. Epub 2011 May 31. No abstract available.

4.

DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil.

Cardoso GL, Diniz IG, Silva AN, Cunha DA, Silva Junior JS, Uchôa CT, Santos SE, Trindade SM, Cardoso Mdo S, Guerreiro JF.

Blood Cells Mol Dis. 2014 Dec;53(4):176-9. doi: 10.1016/j.bcmd.2014.07.006. Epub 2014 Jul 30.

5.

Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia.

Nagel RL, Steinberg MH.

Pediatr Pathol Mol Med. 2001 Mar-Apr;20(2):123-36. Review.

PMID:
12673837
6.

5' hypersensitive site-2 and fetal hemoglobin in Brazilians.

Figueirido MS, Steinberg MH.

Hemoglobin. 1996 Nov;20(4):435-8. No abstract available.

PMID:
8936469
7.

Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models.

Milton JN, Gordeuk VR, Taylor JG 6th, Gladwin MT, Steinberg MH, Sebastiani P.

Circ Cardiovasc Genet. 2014 Apr;7(2):110-5. doi: 10.1161/CIRCGENETICS.113.000387. Epub 2014 Mar 1.

8.

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
9.

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.

10.

BetaS-haplotypes in sickle cell anemia patients from Salvador, Bahia, Northeastern Brazil.

Gonçalves MS, Bomfim GC, Maciel E, Cerqueira I, Lyra I, Zanette A, Bomfim G, Adorno EV, Albuquerque AL, Pontes A, Dupuit MF, Fernandes GB, dos Reis MG.

Braz J Med Biol Res. 2003 Oct;36(10):1283-8. Epub 2003 Sep 16.

11.

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.

12.

Genetic disorders of hemoglobin synthesis.

Bank A.

Hosp Pract (Off Ed). 1985 Sep 15;20(9):109-11, 115-9, 123-4. No abstract available.

PMID:
2411743
13.
14.

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.

15.

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.

16.

Senegal haplotype is associated with higher HbF than Benin and Cameroon haplotypes in African children with sickle cell anemia.

Green NS, Fabry ME, Kaptue-Noche L, Nagel RL.

Am J Hematol. 1993 Oct;44(2):145-6. No abstract available.

PMID:
7505527
17.

Effects of hydroxyurea in a population of Brazilian patients with sickle cell anemia.

Vicari P, Barretto de Mello A, Figueiredo MS.

Am J Hematol. 2005 Mar;78(3):243-4.

18.

Beta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California.

Schroeder WA, Powars DR, Kay LM, Chan LS, Huynh V, Shelton JB, Shelton JR.

Hemoglobin. 1989;13(4):325-53.

PMID:
2473969
19.

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
20.

Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans.

Bae HT, Baldwin CT, Sebastiani P, Telen MJ, Ashley-Koch A, Garrett M, Hooper WC, Bean CJ, Debaun MR, Arking DE, Bhatnagar P, Casella JF, Keefer JR, Barron-Casella E, Gordeuk V, Kato GJ, Minniti C, Taylor J, Campbell A, Luchtman-Jones L, Hoppe C, Gladwin MT, Zhang Y, Steinberg MH.

Blood. 2012 Aug 30;120(9):1961-2. doi: 10.1182/blood-2012-06-432849. No abstract available.

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