Showing results (171-180 of 2,197) with videos related to

Sort By:
Pageof 220
Blood Cells, Molecules & Diseases|September 23, 2000
Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneityG Papanikolaou, M Politou, E Terpos, et al.
Blood Cells, Molecules & Diseases|March 22, 2001
Identification and validation of candidate Myb target genesP A Bartley, J K Lutwyche, T J Gonda
Blood Cells, Molecules & Diseases|January 11, 2002
A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidinP L Lee, T Gelbart, C West, et al.
Blood Cells, Molecules & Diseases|January 11, 2002
A region upstream of the human delta-globin gene shows a stage-specific interaction with globin promoters in erythroid cell linesM Vitale, R Calzolari, R Di Marzo, et al.
Blood Cells, Molecules & Diseases|January 11, 2002
Monitoring of MRP-like activity in human erythrocytes: inhibitory effect of isoflavonesM Bobrowska-Hägerstrand, A Wróbel, B Rychlik, et al.
Blood Cells, Molecules & Diseases|November 27, 1999
The consequence of nucleotide substitutions in the triosephosphate isomerase (TPI) gene promoterA Humphries, A Ationu, B Wild, et al.
Blood Cells, Molecules & Diseases|November 27, 1999
Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopeniaL J Thompson, M R Lalloz, D M Layton
Blood Cells, Molecules & Diseases|November 27, 1999
Analysis of blood coagulation in the zebrafishP Jagadeeswaran, J P Sheehan
Blood Cells, Molecules & Diseases|December 9, 2000
A new gene-pseudogene fusion allele due to a recombination in intron 2 of the glucocerebrosidase gene causes Gaucher diseaseB Cormand, A Díaz, D Grinberg, et al.
Blood Cells, Molecules & Diseases|December 9, 2000
Erythropoietin-dependent suppression of the expression of the beta subunits of the interleukin-3 receptor during erythroid differentiationC Carta, S Campisi, G Migliaccio, et al.
Pageof 220