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Blood Cells, Molecules & Diseases|November 22, 2016
Combined beta-glucosylceramide and ambroxol hydrochloride in patients with Gaucher related Parkinson disease: From clinical observations to drug developmentYuval Ishay, Ari Zimran, Jeffrey Szer, et al.Blood Cells, Molecules & Diseases|February 12, 2014
DNMT3A R882 mutations in patients with cytogenetically normal acute myeloid leukemia and myelodysplastic syndromeDoaa El Ghannam, Mona M Taalab, Hayam F Ghazy, et al.Blood Cells, Molecules & Diseases|May 31, 2008
The hemolysis kinetics of psoriatic red blood cellsA GórnickiBlood Cells, Molecules & Diseases|February 19, 2014
The spectrum of α- and β-thalassemia mutations of the Li people in Hainan Province of ChinaHongxia Yao, Xinping Chen, Lie Lin, et al.Blood Cells, Molecules & Diseases|February 4, 2014
DNA damage response in adult stem cellsAlessandra Insinga, Angelo Cicalese, Pier Giuseppe PelicciBlood Cells, Molecules & Diseases|March 6, 2014
The RNA in reticulocytes is not just debris: it is necessary for the final stages of erythrocyte formationEunMi Lee, Hye Sook Choi, Jung Hye Hwang, et al.Blood Cells, Molecules & Diseases|March 8, 2014
Inhibition of DPP4/CD26 and dmPGE₂ treatment enhances engraftment of mouse bone marrow hematopoietic stem cellsHal E Broxmeyer, Louis M PelusBlood Cells, Molecules & Diseases|March 4, 2014
Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysisNaruwat Pakdee, Supawadee Yamsri, Goonnapa Fucharoen, et al.Blood Cells, Molecules & Diseases|April 3, 2008
Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao familyPeng Yi, Fang Yu, Shengwei Huang, et al.Blood Cells, Molecules & Diseases|October 21, 2018
Detection of HFE Haemochromatosis in the clinic and community using standard erythrocyte testsNiwansa Adris, Simon Hazeldine, Peter Bentley, et al.Pageof 220