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Similar articles for PubMed (Select 19344402)

1.

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
2.

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, Araújo 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.

3.

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
4.

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications.

Thein SL, Menzel S, Lathrop M, Garner C.

Hum Mol Genet. 2009 Oct 15;18(R2):R216-23. doi: 10.1093/hmg/ddp401. Review.

5.

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.

Uda M, Galanello R, Sanna S, Lettre G, Sankaran VG, Chen W, Usala G, Busonero F, Maschio A, Albai G, Piras MG, Sestu N, Lai S, Dei M, Mulas A, Crisponi L, Naitza S, Asunis I, Deiana M, Nagaraja R, Perseu L, Satta S, Cipollina MD, Sollaino C, Moi P, Hirschhorn JN, Orkin SH, Abecasis GR, Schlessinger D, Cao A.

Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1620-5. doi: 10.1073/pnas.0711566105. Epub 2008 Feb 1.

6.

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
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.

[Progress on genes related to fetal hemoglobin quantitative trait].

Guo XQ.

Yi Chuan. 2010 Apr;32(4):295-300. Review. Chinese.

PMID:
20423883
9.

Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania.

Mtatiro SN, Makani J, Mmbando B, Thein SL, Menzel S, Cox SE.

Am J Hematol. 2015 Jan;90(1):E1-4. doi: 10.1002/ajh.23859. Epub 2014 Oct 20.

PMID:
25263325
10.

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.

PMID:
17918249
11.

Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.

Makani J, Menzel S, Nkya S, Cox SE, Drasar E, Soka D, Komba AN, Mgaya J, Rooks H, Vasavda N, Fegan G, Newton CR, Farrall M, Thein SL.

Blood. 2011 Jan 27;117(4):1390-2. doi: 10.1182/blood-2010-08-302703. Epub 2010 Nov 10.

12.

BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.

Sedgewick AE, Timofeev N, Sebastiani P, So JC, Ma ES, Chan LC, Fucharoen G, Fucharoen S, Barbosa CG, Vardarajan BN, Farrer LA, Baldwin CT, Steinberg MH, Chui DH.

Blood Cells Mol Dis. 2008 Nov-Dec;41(3):255-8. doi: 10.1016/j.bcmd.2008.06.007. Epub 2008 Aug 8.

13.

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.

Thein SL, Menzel S, Peng X, Best S, Jiang J, Close J, Silver N, Gerovasilli A, Ping C, Yamaguchi M, Wahlberg K, Ulug P, Spector TD, Garner C, Matsuda F, Farrall M, Lathrop M.

Proc Natl Acad Sci U S A. 2007 Jul 3;104(27):11346-51. Epub 2007 Jun 25.

14.

Association of Xmn1 -158 γG variant with severity and HbF levels in β-thalassemia major and sickle cell anaemia.

Dadheech S, Jain S, Madhulatha D, Sharma V, Joseph J, Jyothy A, Munshi A.

Mol Biol Rep. 2014 May;41(5):3331-7. doi: 10.1007/s11033-014-3195-5. Epub 2014 Feb 2.

PMID:
24488321
15.

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression.

Farrell JJ, Sherva RM, Chen ZY, Luo HY, Chu BF, Ha SY, Li CK, Lee AC, Li RC, Li CK, Yuen HL, So JC, Ma ES, Chan LC, Chan V, Sebastiani P, Farrer LA, Baldwin CT, Steinberg MH, Chui DH.

Blood. 2011 May 5;117(18):4935-45. doi: 10.1182/blood-2010-11-317081. Epub 2011 Mar 8.

16.

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
17.

Influences of genetic variation on fetal hemoglobin.

He Y, Lin W, Luo J.

Pediatr Hematol Oncol. 2011 Nov;28(8):708-17. doi: 10.3109/08880018.2011.616573.

PMID:
22023465
18.

Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia.

Papachatzopoulou A, Kourakli A, Makropoulou P, Kakagianne T, Sgourou A, Papadakis M, Athanassiadou A.

Eur J Haematol. 2006 Apr;76(4):322-30.

PMID:
16519704
19.

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.

20.

Haemoglobin F levels in healthy Nigerian adults.

Kotila TR, Shokunbi WA.

West Afr J Med. 2003 Jun;22(2):143-5.

PMID:
14529224
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