Cargando…
Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patients
BACKGROUND: Human erythropoiesis is characterized by distinct gene expression profiles at various developmental stages. Previous studies suggest that fetal-to-adult hemoglobin switch is regulated by a complex mechanism, in which many key players still remain unknown. Here, we report our findings fro...
Autores principales: | Chondrou, Vasiliki, Kolovos, Petros, Sgourou, Argyro, Kourakli, Alexandra, Pavlidaki, Alexia, Kastrinou, Vlasia, John, Anne, Symeonidis, Argiris, Ali, Bassam R., Papachatzopoulou, Adamantia, Katsila, Theodora, Patrinos, George P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654038/ https://www.ncbi.nlm.nih.gov/pubmed/29061162 http://dx.doi.org/10.1186/s40246-017-0120-8 |
Ejemplares similares
-
Impact of ZBTB7A hypomethylation and expression patterns on treatment response to hydroxyurea
por: Chondrou, Vasiliki, et al.
Publicado: (2018) -
The multi-faceted functioning portrait of LRF/ZBTB7A
por: Constantinou, Caterina, et al.
Publicado: (2019) -
Contingent Synergistic Interactions between Non-Coding RNAs and DNA-Modifying Enzymes in Myelodysplastic Syndromes
por: Symeonidis, Argiris, et al.
Publicado: (2022) -
Association of genome variations in the renin-angiotensin system with physical performance
por: Sgourou, Argyro, et al.
Publicado: (2012) -
P-075: HYDROXYUREA: EFFECTS ON TREATMENT OF CHILDREN WITH HEMOGLOBINOPATHY SC
por: A., CAMPOS, et al.
Publicado: (2022)