Genetic reversal of the globin switch concurrently modulates both fetal and sickle hemoglobin and reduces red cell sickling
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
-
Genetic reversal of the globin switch concurrently modulates both fetal and sickle hemoglobin and reduces red cell sickling ; volume:14 ; number:1 ; day:20 ; month:9 ; year:2023 ; pages:1-10 ; date:12.2023
Nature Communications ; 14, Heft 1 (20.9.2023), 1-10, 12.2023
- Creator
-
Souza, Daniel C. De
Hebert, Nicolas
Esrick, Erica B.
Ciuculescu, M. Felicia
Archer, Natasha M.
Armant, Myriam
Audureau, Étienne
Brendel, Christian
Caprio, Giuseppe Di
Galactéros, Frédéric
Liu, Donghui
McCabe, Amanda
Morris, Emily
Schonbrun, Ethan
Williams, Dillon
Wood, David K.
Williams, David A.
Bartolucci, Pablo
Higgins, John M.
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1038/s41467-023-40923-5
- URN
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urn:nbn:de:101:1-2024020210422695945622
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:37 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Souza, Daniel C. De
- Hebert, Nicolas
- Esrick, Erica B.
- Ciuculescu, M. Felicia
- Archer, Natasha M.
- Armant, Myriam
- Audureau, Étienne
- Brendel, Christian
- Caprio, Giuseppe Di
- Galactéros, Frédéric
- Liu, Donghui
- McCabe, Amanda
- Morris, Emily
- Schonbrun, Ethan
- Williams, Dillon
- Wood, David K.
- Williams, David A.
- Bartolucci, Pablo
- Higgins, John M.
- SpringerLink (Online service)
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Gum Arabic as fetal hemoglobin inducing agent in sickle cell anemia; in vivo study
The globin gene family of the cephalochordate amphioxus: implications for chordate globin evolution
Base-editing-mediated dissection of a γ-globin cis-regulatory element for the therapeutic reactivation of fetal hemoglobin expression
Classical sickle beta-globin haplotypes exhibit a high degree of long-range haplotype similarity in African and Afro-Caribbean populations
An Aγ-globin G->A gene polymorphism associated with β039 thalassemia globin gene and high fetal hemoglobin production
Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants
Fetal hemoglobin level and nutritional status in patients with sickle cell disease
Expression der Gene β-Globin [Beta-Globin], γ-Globin [Gamma-Globin] und Glycophorin A in myeloischen Kolonien bei Kindern mit juveniler myelomonozytärer Leukämie
Expression der Gene β-Globin [Beta-Globin], y-Globin [Gamma-Globin] und Glycophorin A in myeloischen Kolonien bei Kindern mit juveniler myelomonozytärer Leukämie
The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease
Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia
Correlates of Pulmonary Function in Children with Sickle Cell Disease and Elevated Fetal Hemoglobin
Gum Arabic as fetal hemoglobin inducing agent in sickle cell anemia; in vivo study
The globin gene family of the cephalochordate amphioxus: implications for chordate globin evolution
Base-editing-mediated dissection of a γ-globin cis-regulatory element for the therapeutic reactivation of fetal hemoglobin expression
Classical sickle beta-globin haplotypes exhibit a high degree of long-range haplotype similarity in African and Afro-Caribbean populations
An Aγ-globin G->A gene polymorphism associated with β039 thalassemia globin gene and high fetal hemoglobin production
Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants
Fetal hemoglobin level and nutritional status in patients with sickle cell disease
Expression der Gene β-Globin [Beta-Globin], γ-Globin [Gamma-Globin] und Glycophorin A in myeloischen Kolonien bei Kindern mit juveniler myelomonozytärer Leukämie
Expression der Gene β-Globin [Beta-Globin], y-Globin [Gamma-Globin] und Glycophorin A in myeloischen Kolonien bei Kindern mit juveniler myelomonozytärer Leukämie
The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease
Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia
Correlates of Pulmonary Function in Children with Sickle Cell Disease and Elevated Fetal Hemoglobin
Gum Arabic as fetal hemoglobin inducing agent in sickle cell anemia; in vivo study
The globin gene family of the cephalochordate amphioxus: implications for chordate globin evolution
Base-editing-mediated dissection of a γ-globin cis-regulatory element for the therapeutic reactivation of fetal hemoglobin expression