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American Journal of Respiratory and Critical Care Medicine|October 21, 2017
Red Blood Cells Homeostatically Bind Mitochondrial DNA through TLR9 to Maintain Quiescence and to Prevent Lung InjuryMeghan J Hotz, Danielle Qing, Michael G S Shashaty, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 28, 2013
Intestinal HIF2α promotes tissue-iron accumulation in disorders of iron overload with anemiaErik R Anderson, Matthew Taylor, Xiang Xue, et al.
British Journal of Haematology|August 31, 2006
Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic seraOrly Weizer-Stern, Konstantin Adamsky, Ninette Amariglio, et al.
Plos One|December 10, 2021
Tmprss6-ASO as a tool for the treatment of Polycythemia Vera miceCarla Casu, Alison Liu, Gianluca De Rosa, et al.
The Journal of Clinical Investigation|July 19, 2013
Isocitrate ameliorates anemia by suppressing the erythroid iron restriction responseChanté L Richardson, Lorrie L Delehanty, Grant C Bullock, et al.
European Journal of Haematology|October 14, 2014
Altered erythropoiesis and iron metabolism in carriers of thalassemiaJacqueline S Guimarães, Juçara G Cominal, Ana Cristina Silva-Pinto, et al.
Biotechnology and Applied Biochemistry|February 17, 2009
Development of K562 cell clones expressing beta-globin mRNA carrying the beta039 thalassaemia mutation for the screening of correctors of stop-codon mutationsFrancesca Salvatori, Vera Cantale, Giulia Breveglieri, et al.
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