Analyzing 5′HS3 and 5′HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations-Reference-Cited by-同舟云学术

Analyzing 5′HS3 and 5′HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations

Published:2011-03 Issue:3 Volume:46 Page:201-205
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Neishabury Maryam,Azarkeivan Azita,Oberkanins Christian,Abedini Seyedeh Sedigheh,Zamani Shahbaz,Najmabadi Hossein

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference33 articles.

1. Fourteen-year experience of prenatal diagnosis of thalassemia in Iran;Najmabadi;Community Genet.,2006

2. Thalassemia in Iran: epidemiology, prevention, and management;Abolghasemi;J. Pediatr. Hematol. Oncol.,2007

3. Lessons from thalassaemia screening in Iran;Christianson;BMJ,2004

4. Molecular mechanisms underlying thalassemia intermedia in Iran;Neishabury;Genet. Test,2008

5. Joining the loops: beta-globin gene regulation;Noordermeer;IUBMB Life,2008

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1. The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background;Blood Cells, Molecules, and Diseases;2013-08

2. Annotated Definition of BCL11A and HMIP-2 Haplotypes Through the Analysis of Sicilian β-Thalassemia Patients with High Levels of Fetal Hemoglobin;Hemoglobin;2013-06-19

3. The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5′HS4;Blood Cells, Molecules, and Diseases;2012-01