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Hemoglobin
international journal for hemoglobin research
Volume 37, 2013 - Issue 6
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Original Article

Gene Expression Analysis of the Brazilian Type of Hereditary Persistence of Fetal Hemoglobin: Identification of Genes that Could be Related to γ-Globin Activation

Fernanda Marconi RoversiHematology and Hemotherapy Center, University of Campinas (UNICAMP), Campinas, São Paulo, Brasil
,
Anderson Ferreira da CunhaDepartment of Genetic and Evolution, Federal University of São Carlos (UFSCAR), São Carlos, São Paulo, Brasil
,
Ana Flávia BrugnerottoHematology and Hemotherapy Center, University of Campinas (UNICAMP), Campinas, São Paulo, Brasil
,
Marcelo Falsarella CarazzolleDepartment of Genetics and Evolution, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil
,
Dulcinéia Martins de AlbuquerqueHematology and Hemotherapy Center, University of Campinas (UNICAMP), Campinas, São Paulo, Brasil
,
Carolina LanaroHematology and Hemotherapy Center, University of Campinas (UNICAMP), Campinas, São Paulo, Brasil
,
João Agostinho Machado-NetoHematology and Hemotherapy Center, University of Campinas (UNICAMP), Campinas, São Paulo, Brasil
,
Sara Teresinha Olalla SaadHematology and Hemotherapy Center, University of Campinas (UNICAMP), Campinas, São Paulo, Brasil
&
Fernando Ferreira da CostaHematology and Hemotherapy Center, University of Campinas (UNICAMP), Campinas, São Paulo, BrasilCorrespondence[email protected]
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Pages 516-535 | Received 27 Nov 2012, Accepted 07 Apr 2013, Published online: 19 Aug 2013

Citations (3)

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Read on this site (1)

Ahmad Tamaddoni, Sahar Khabaz Astaneh, Reza Tabaripour & Haleh Akhavan-Niaki. (2019) Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia. Hemoglobin 43:1, pages 12-17.
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Articles from other publishers (2)

Guoqiang Zhou & Daru Lu. (2023) Proteomics screening uncovers HMGA1 as a promising negative regulator for γ-globin expression in response to decreased β-globin levels. Journal of Proteomics 286, pages 104957.
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Beeke Wienert, Alister P. W. Funnell, Laura J. Norton, Richard C. M. Pearson, Lorna E. Wilkinson-White, Krystal Lester, Jim Vadolas, Matthew H. Porteus, Jacqueline M. Matthews, Kate G. R. Quinlan & Merlin Crossley. (2015) Editing the genome to introduce a beneficial naturally occurring mutation associated with increased fetal globin. Nature Communications 6:1.
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