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Blood Cells, Molecules & Diseases|November 3, 2007
Photodynamic purging of alloreactive T cells for adoptive immunotherapy after haploidentical stem cell transplantationKatia Perruccio, Fabiana Topini, Antonella Tosti, et al.Blood Cells, Molecules & Diseases|October 30, 2007
A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemiaPrabhakar S Kedar, Prashant Warang, Anita H Nadkarni, et al.Blood Cells, Molecules & Diseases|October 30, 2007
Immunogenetic factors in donors and patients that affect the outcome of hematopoietic stem cell transplantationAlejandro Madrigal, Bronwen E ShawBlood Cells, Molecules & Diseases|October 30, 2007
Reduced erythroid cell and erythropoietin production in response to acute anemia in prion protein-deficient (Prnp-/-) miceJan H Zivny, Monique P Gelderman, Fei Xu, et al.Blood Cells, Molecules & Diseases|August 11, 2007
The role of STAT, AP-1, E-box and TIEG motifs in the regulation of hepcidin by IL-6 and BMP-9: lessons from human HAMP and murine Hamp1 and Hamp2 gene promotersJaroslav Truksa, Pauline Lee, Ernest BeutlerBlood Cells, Molecules & Diseases|November 11, 2008
Staging multiple myeloma patients with active disease using serum levels of beta2m-free HLA class I heavy chain together with IgM or platelet countFederico Perosa, Carla Minoia, Elvira Favoino, et al.Blood Cells, Molecules & Diseases|April 3, 2012
Refined views of multi-protein complexes in the erythrocyte membraneT J Mankelow, T J Satchwell, N M BurtonBlood Cells, Molecules & Diseases|December 3, 2011
ABCB1 haplotype is associated with major molecular response in chronic myeloid leukemia patients treated with standard-dose of imatinibDouglas Vivona, Carolina T Bueno, Luciene T Lima, et al.Blood Cells, Molecules & Diseases|August 17, 2011
Iron chelation therapy in thalassemia major: a systematic review with meta-analyses of 1520 patients included on randomized clinical trialsAurelio Maggio, Aldo Filosa, Angela Vitrano, et al.Blood Cells, Molecules & Diseases|February 3, 2012
Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosisAi Hattori, Naohisa Tomosugi, Yasuaki Tatsumi, et al.Pageof 220