A novel deletion causing α thalassemia clarifies the importance of the major human alpha globin regulatory element-Reference-Cited by-同舟云学术

A novel deletion causing α thalassemia clarifies the importance of the major human alpha globin regulatory element

Published:2006-05-01 Issue:9 Volume:107 Page:3811-3812
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Viprakasit Vip,Harteveld Cornelis L.,Ayyub Helena,Stanley Jackie S.,Giordano Piero C.,Wood William G.,Higgs Douglas R.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/107/9/3811/469996/zh800906003811.pdf

Reference10 articles.

1. Hughes JR, Cheng JF, Ventress N, et al. Annotation of cis-regulatory elements by identification, subclassification, and functional assessment of multispecies conserved sequences. Proc Natl Acad Sci U S A. 2005;102: 9830-9835.

2. Higgs DR, Wood WG, Jarman AP, et al. A major positive regulatory region located far upstream of the human alpha-globin gene locus. Genes Dev. 1990;4: 1588-1601.

3. Hatton CS, Wilkie AO, Drysdale HC, et al. Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster. Blood. 1990; 76: 221-227.

4. Higgs DR. Molecular mechanisms of α thalassemia. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, eds. Disorders of Hemoglobin. Cambridge, United Kingdom: Cambridge University Press; 2001: 405-430.

5. Viprakasit V, Kidd AM, Ayyub H, Horsley S, Hughes J, Higgs DR. De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia. Br J Haematol. 2003;120: 867-875.

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