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Blood Cells, Molecules & Diseases|May 16, 2015
Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genesFrancesca Clementina Radio, Silvia Majore, Caterina Aurizi, et al.
Blood Cells, Molecules & Diseases|May 31, 2020
Biomedical article authorship: A proposal to enhance the meaningful assignment of authorshipMarshall A Lichtman
Blood Cells, Molecules & Diseases|June 20, 2020
Hypoxia induced up-regulation of tissue factor is mediated through extracellular RNA activated Toll-like receptor 3-activated protein 1 signallingSaumya Bhagat, Indranil Biswas, Rehan Ahmed, et al.
Blood Cells, Molecules & Diseases|August 16, 2005
Enhancement of growth and survival and alterations in Bcl-family proteins in beta-thalassemic erythroid progenitors by novel short-chain fatty acid derivativesSerguei Castaneda, Michael S Boosalis, David Emery, et al.
Blood Cells, Molecules & Diseases|October 6, 2005
Exosomes contain ubiquitinated proteinsSonja I Buschow, Jolanda M P Liefhebber, Richard Wubbolts, et al.
Blood Cells, Molecules & Diseases|August 1, 2006
Enhanced oxidative cross-linking of hemoglobin E with spectrin and loss of erythrocyte membrane asymmetry in hemoglobin Ebeta-thalassemiaPoppy Datta, Sumanta Basu, Sudipa Basu Chakravarty, et al.
Blood Cells, Molecules & Diseases|September 12, 2006
Relationship between polymorphisms in thrombophilic genes and preeclampsia in a Brazilian populationC A Dalmáz, K G Santos, M R Botton, et al.
Blood Cells, Molecules & Diseases|August 15, 2006
Stimulation of non-transferrin iron uptake by iron deprivation in K562 cellsJan Kovar, Jitka Neubauerova, Marketa Cimburova, et al.
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