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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|October 31, 2018
Green tea extract modulates oxidative tissue injury in beta-thalassemic mice by chelation of redox iron and inhibition of lipid peroxidationPimpisid Koonyosying, Sarawut Kongkarnka, Chairat Uthaipibull, et al.
Scientific Reports|May 23, 2019
Restoration of correct βIVS2-654-globin mRNA splicing and HbA production by engineered U7 snRNA in β-thalassaemia/HbE erythroid cellsTiwaporn Nualkaew, Natee Jearawiriyapaisarn, Suradej Hongeng, et al.
Journal of Natural Products|March 4, 2010
Labdane diterpenes from the aerial parts of Curcuma comosa enhance fetal hemoglobin production in an erythroid cell lineRatchanaporn Chokchaisiri, Nattawara Chaneiam, Saovaros Svasti, et al.
Free Radical Research|March 26, 2003
Hemin: a possible cause of oxidative stress in blood circulation of beta-thalassemia/hemoglobin E diseaseNoppawan Phumala, Supatra Porasuphatana, Supeenun Unchern, et al.
American Journal of Hematology|July 12, 2002
Increased circulating activated endothelial cells, vascular endothelial growth factor, and tumor necrosis factor in thalassemiaPunnee Butthep, Saknarong Rummavas, Raewadee Wisedpanichkij, et al.
Frontiers in Genetics|August 28, 2020
Genome-Wide Transcriptional Regulation of the Long Non-coding RNA Steroid Receptor RNA Activator in Human ErythroblastsWaritta Sawaengdee, Kairong Cui, Keji Zhao, et al.
Biochemical and Biophysical Research Communications|March 11, 2008
Inhibition of alpha-globin gene expression by RNAiOrawan Sarakul, Phantip Vattanaviboon, Prapon Wilairat, et al.
Magnetic Resonance Imaging|May 26, 2019
MRI imaging and histopathological study of brain iron overload of β-thalassemic miceParanee Yatmark, Somkiat Huaijantug, Wuttiwong Teerapan, et al.
Annals of Hematology|January 12, 2011
Enhanced activation of autophagy in β-thalassemia/Hb E erythroblasts during erythropoiesisPathrapol Lithanatudom, Tirawat Wannatung, Amporn Leecharoenkiat, et al.
International Journal of Hematology|October 26, 2017
Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β0-thalassemia/HbE diseasePinyaphat Khamphikham, Orapan Sripichai, Thongperm Munkongdee, et al.
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