Annotated Definition of BCL11A and HMIP-2 Haplotypes Through the Analysis of Sicilian β-Thalassemia Patients with High Levels of Fetal Hemoglobin-Reference-Cited by-同舟云学术

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

Published:2013-06-19 Issue:5 Volume:37 Page:423-434
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Buccheri Maria A.,Spina Sonia,Ruberto Concetta,Lombardo Turi,Labie Dominique,Ragusa and Angela

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2013.800823

Reference30 articles.

1. Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific Repressor BCL11A

2. Transcriptional silencing of γ-globin by BCL11A involves long-range interactions and cooperation with SOX6

3. Correction of Sickle Cell Disease in Adult Mice by Interference with Fetal Hemoglobin Silencing

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

5. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Homozygous KLF1 mutation c.901C>T (p.Arg301Cys) resulting in mild thalassemia intermedia in an Indian: A next-generation sequencing diagnosis;Blood Cells, Molecules, and Diseases;2018-09

2. MicroRNAs in erythropoiesis and red blood cell disorders;Frontiers in Biology;2015-07-30

3. Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child;Pediatric Hematology and Oncology;2015-06-18

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