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Items: 1 to 20 of 217

1.

Xmn I polymorphism associated with concomitant activation of Gγ and Aγ globin gene transcription on a β0-thalassemia chromosome.

Haj Khelil A, Morinière M, Laradi S, Khelif A, Perrin P, Ben Chibani J, Baklouti F.

Blood Cells Mol Dis. 2011 Feb 15;46(2):133-8. doi: 10.1016/j.bcmd.2010.11.002. Epub 2010 Dec 8.

PMID:
21144779
3.

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
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α-Haemoglobin stabilising protein expression is influenced by mean cell haemoglobin and HbF levels in HbE/β-thalassaemia individuals.

Lim WF, Muniandi L, George E, Sathar J, Teh LK, Gan GG, Lai MI.

Blood Cells Mol Dis. 2012 Jan 15;48(1):17-21. doi: 10.1016/j.bcmd.2011.10.002. Epub 2011 Nov 12.

PMID:
22079025
9.
10.

Molecular characterization of β-thalassemia intermedia: a report from Iran.

Arab A, Karimipoor M, Rajabi A, Hamid M, Arjmandi S, Zeinali S.

Mol Biol Rep. 2011 Oct;38(7):4321-6. doi: 10.1007/s11033-010-0557-5. Epub 2010 Dec 1.

PMID:
21120615
11.
12.

The Xmn I site (-158, C----T) 5' to the G gamma gene: correlation with the Senegalese haplotype and G gamma globin expression.

Ballas SK, Talacki CA, Adachi K, Schwartz E, Surrey S, Rappaport E.

Hemoglobin. 1991;15(5):393-405.

PMID:
1724976
13.

A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and beta-thalassemia compound heterozygotes.

Papadakis MN, Patrinos GP, Tsaftaridis P, Loutradi-Anagnostou A.

J Mol Med (Berl). 2002 Apr;80(4):243-7. Epub 2001 Dec 18.

PMID:
11976733
14.

Delayed decline of gamma-globin expression in infant age associated with the presence of Ggamma-158 (C-->T) polymorphism.

Grosso M, Amendolara M, Rescigno G, Danise P, Todisco N, Izzo P, Amendola G.

Int J Lab Hematol. 2008 Jun;30(3):191-5. doi: 10.1111/j.1751-553X.2007.00946.x.

PMID:
18479296
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16.

Combined effect of two different polymorphic sequences within the beta globin gene cluster on the level of HbF.

Gonçalves I, Ducrocq R, Lavinha J, Nogueira PJ, Peres MJ, Picanço I, Correia E Jr, Reis AB, Silva C, Krishnamoorthy R, Almeida LO.

Am J Hematol. 1998 Apr;57(4):269-76.

17.

Increased expression of the G gamma and A gamma globin genes associated with a mutation in the A gamma enhancer.

Balta G, Brickner HE, Takegawa S, Kazazian HH Jr, Papayannopoulou T, Forget BG, Atweh GF.

Blood. 1994 Jun 15;83(12):3727-37.

18.

Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.

Beris P, Kitundu MN, Baysal E, Oner C, Lanclos KD, Dimovski AJ, Kutlar F, Huisman TH.

Am J Hematol. 1992 Oct;41(2):97-101.

PMID:
1384315
19.

Structural and Functional Insights on an Uncharacterized Aγ-Globin-Gene Polymorphism Present in Four β0-Thalassemia Families with High Fetal Hemoglobin Levels.

Bianchi N, Cosenza LC, Lampronti I, Finotti A, Breveglieri G, Zuccato C, Fabbri E, Marzaro G, Chilin A, De Angelis G, Borgatti M, Gallucci C, Alfieri C, Ribersani M, Isgrò A, Marziali M, Gaziev J, Morrone A, Sodani P, Lucarelli G, Gambari R, Paciaroni K.

Mol Diagn Ther. 2016 Apr;20(2):161-73. doi: 10.1007/s40291-016-0187-2.

PMID:
26897028

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