Physiological and Aberrant γ-Globin Transcription During Development
The expression of the fetal Gγ- and Aγ-globin genes in normal development is confined to the fetal period, where two γ-globin chains assemble with two α-globin chains to form α2γ2 tetramers (HbF). HbF sustains oxygen delivery to tissues until birth, when β-globin replaces γ-globin, leading to the fo...
Main Authors: | Gloria Barbarani, Agata Labedz, Sarah Stucchi, Alessia Abbiati, Antonella E. Ronchi |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2021-04-01
|
Series: | Frontiers in Cell and Developmental Biology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fcell.2021.640060/full |
Similar Items
-
β-Hemoglobinopathies: The Test Bench for Genome Editing-Based Therapeutic Strategies
by: Gloria Barbarani, et al.
Published: (2020-12-01) -
Mild dyserythropoiesis and β-like globin gene expression imbalance due to the loss of histone chaperone ASF1B
by: Petros Papadopoulos, et al.
Published: (2020-10-01) -
Fetal Hemoglobin in Sickle Hemoglobinopathies: High HbF Genotypes and Phenotypes
by: Martin H. Steinberg
Published: (2020-11-01) -
Molecular identification of Sicilian (<FONT FACE=Symbol>dß)º-thalassemia associated with ß-thalassemia and hemoglobin S in Brazil</FONT>
by: T.G. de Andrade, et al.
Published: (2002-08-01) -
Molecular identification of Sicilian (dß)º-thalassemia associated with ß-thalassemia and hemoglobin S in Brazil
by: Andrade T.G. de, et al.
Published: (2002-01-01)