Individualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patients.
about
Current and future alternative therapies for beta-thalassemia majorRecent trends in the gene therapy of β-thalassemia.Population Screening for Hemoglobinopathy Profiling: Is the Development of a Microarray Worthwhile?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 patientsPharmacogenomics of sickle cell disease: steps toward personalized medicine.Pharmacogenomics education and research at the Department of Pharmacy, University of Patras, Greece.Correlation of SIN3A genomic variants with β-hemoglobinopathies disease severity and hydroxyurea treatment efficacy.Genomic variants in the ASS1 gene, involved in the nitric oxide biosynthesis and signaling pathway, predict hydroxyurea treatment efficacy in compound sickle cell disease/β-thalassemia patients.
P2860
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P2860
Individualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patients.
description
2014 nî lūn-bûn
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name
Individualizing fetal hemoglob ...... e hemoglobinopathies patients.
@en
type
label
Individualizing fetal hemoglob ...... e hemoglobinopathies patients.
@en
prefLabel
Individualizing fetal hemoglob ...... e hemoglobinopathies patients.
@en
P2093
P2860
P356
P1433
P1476
Individualizing fetal hemoglob ...... e hemoglobinopathies patients.
@en
P2093
Adamantia Papachatzopoulou
Aikaterini Gravia
Argyro Sgourou
George P Patrinos
Ioanna Papantoni
Joseph Borg
Vasiliki Chondrou
P2860
P304
P356
10.2217/PGS.14.101
P577
2014-07-01T00:00:00Z