Fetal Hemoglobin Inducers from the Natural World: A Novel Approach for Identification of Drugs for the Treatment of {beta}-Thalassemia and Sickle-Cell Anemia.
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α:Non-α and Gγ:Aγ globin chain ratios in thalassemia intermedia patients treated with hydroxyurea.Fetal globin induction in beta-thalassemia.Characterization of the transcriptome profiles related to globin gene switching during in vitro erythroid maturation.The in vitro antisickling and antioxidant effects of aqueous extracts Zanthoxyllum heitzii on sickle cell disorder.Screening Antitumor Compounds Psoralen and Isopsoralen from Psoralea corylifolia L. SeedsDissection of the radical reactions linked to fetal hemoglobin reveals enhanced pseudoperoxidase activity.The Ethanol Extract of Fructus trichosanthis Promotes Fetal Hemoglobin Production via p38 MAPK Activation and ERK Inactivation in K562 Cells.Role of XmnIgG Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients.Production of beta-globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous beta(0)39 thalassemia patients.Comparison of in-vitro and in-vivo response to fetal hemoglobin production and γ-mRNA expression by hydroxyurea in Hemoglobinopathies.Alternative options for DNA-based experimental therapy of β-thalassemia.Recent trends for novel options in experimental biological therapy of β-thalassemia.Recent trends in the gene therapy of β-thalassemia.Natural Remedies for the Treatment of Beta-Thalassemia and Sickle Cell Anemia-Current Status and Perspectives in Fetal Hemoglobin Reactivation.Radix Astragali Stimulates p38 MARK Phosphorylation in Pediatric Patients with β-Thalassemia.Piceatannol: a potential futuristic natural stilbene as fetal haemoglobin inducer.Phytochemical and pharmacological properties of essential oils from Cedrus species.C(5) modified uracil derivatives showing antiproliferative and erythroid differentiation inducing activities on human chronic myelogenous leukemia K562 cells.The management of sickle cell disease in a primary care setting.Predictive analyses of biological effects of natural products: from plant extracts to biomolecular laboratory and computer modeling.Foetal haemoglobin inducers and thalassaemia: novel achievements.A reduced curcuminoid analog as a novel inducer of fetal hemoglobin.Pharmacological and molecular approaches for the treatment of β-hemoglobin disorders.Combining gene therapy and fetal hemoglobin induction for treatment of β-thalassemia.Complementary and alternative medicine use in thalassemia patients in Shiraz, southern Iran: A cross-sectional study.
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P2860
Fetal Hemoglobin Inducers from the Natural World: A Novel Approach for Identification of Drugs for the Treatment of {beta}-Thalassemia and Sickle-Cell Anemia.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 11 December 2007
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Fetal Hemoglobin Inducers from ...... ssemia and Sickle-Cell Anemia.
@en
Fetal Hemoglobin Inducers from ...... ssemia and Sickle-Cell Anemia.
@nl
type
label
Fetal Hemoglobin Inducers from ...... ssemia and Sickle-Cell Anemia.
@en
Fetal Hemoglobin Inducers from ...... ssemia and Sickle-Cell Anemia.
@nl
prefLabel
Fetal Hemoglobin Inducers from ...... ssemia and Sickle-Cell Anemia.
@en
Fetal Hemoglobin Inducers from ...... ssemia and Sickle-Cell Anemia.
@nl
P2093
P2860
P50
P356
P1476
Fetal Hemoglobin Inducers from ...... assemia and Sickle-Cell Anemia
@en
P2093
Cristina Zuccato
Ilaria Lampronti
Monica Borgatti
Nicoletta Bianchi
Roberto Gambari
P2860
P304
P356
10.1093/ECAM/NEM139
P577
2007-12-11T00:00:00Z