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Hematology (Amsterdam, Netherlands)|November 22, 2017
Modulation of hepcidin expression by normal control and beta0-thalassemia/Hb E erythroblastsJanejira Jaratsittisin, Wannapa Sornjai, Saovaros Svasti, et al.
Biochemical and Biophysical Research Communications|October 10, 2006
Lipid fluidity at different regions in LDL and HDL of beta-thalassemia/Hb E patientsNoppawan Phumala Morales, Chalermkhwan Charlermchoung, Rataya Luechapudiporn, et al.
Histochemistry and Cell Biology|June 10, 2011
Impaired bone formation and osteopenia in heterozygous β(IVSII-654) knockin thalassemic miceKanogwun Thongchote, Saovaros Svasti, Mayurachat Sa-ardrit, et al.
Haematologica|December 18, 2009
A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E diseasePathrapol Lithanatudom, Amporn Leecharoenkiat, Tirawat Wannatung, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|March 3, 2012
Vitamin E supplement improves erythrocyte membrane fluidity of thalassemia: an ESR spin labeling studyWerasak Sutipornpalangkul, Noppawan Phumala Morales, Supeenun Unchern, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|November 4, 2021
Iron chelation therapy with deferiprone improves oxidative status and red blood cell quality and reduces redox-active iron in β-thalassemia/hemoglobin E patientsNoppawan Phumala Morales, Supot Rodrat, Pannaree Piromkraipak, et al.
British Journal of Haematology|July 15, 2009
Increased erythropoiesis of beta-thalassaemia/Hb E proerythroblasts is mediated by high basal levels of ERK1/2 activationTirawat Wannatung, Pathrapol Lithanatudom, Amporn Leecharoenkiat, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|February 19, 2013
In vitro antimicrobial activity of volatile organic compounds from Muscodor crispans against the pathogenic oomycete Pythium insidiosumTheerapong Krajaejun, Tassanee Lowhnoo, Wanta Yingyong, et al.
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