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Blood Cells, Molecules & Diseases|October 20, 2009
Analysis of malaria associated genetic traits in Cabo Verde, a melting pot of European and sub Saharan settlersJoana Alves, Patrícia Machado, João Silva, et al.Blood Cells, Molecules & Diseases|March 5, 2010
Effect of interleukin-8 and RANTES on the Gardos channel activity in sickle human red blood cells: role of the Duffy antigen receptor for chemokinesMarie-Claude Durpès, Danitza Nebor, Pierre Couespel du Mesnil, et al.Blood Cells, Molecules & Diseases|January 16, 2010
Spontaneous regression of disease manifestations can occur in type 1 Gaucher disease; results of a retrospective cohort studyJooske M F Boomsma, Laura van Dussen, Maaike G Wiersma, et al.Blood Cells, Molecules & Diseases|February 4, 2010
X-linked agammaglobulinemia in a 10-year-old boy with a novel non-invariant splice-site mutation in Btk geneKota Maekawa, Masafumi Yamada, Yuka Okura, et al.Blood Cells, Molecules & Diseases|January 1, 1997
Modulatory subdomains of the HS2 enhancer differentially regulate enhancer activity in erythroid cells at different developmental stagesR Cavallesco, D TuanBlood Cells, Molecules & Diseases|January 1, 1997
Red cell-mediated therapy: opportunities and challengesA KrantzBlood Cells, Molecules & Diseases|December 21, 2005
Mechanisms involved in the swelling of erythrocytes caused by Pacific and Caribbean ciguatoxinsMartin-Pierre Sauviat, Raphaële Boydron-Le Garrec, Jean-Baptiste Masson, et al.Blood Cells, Molecules & Diseases|January 5, 2010
Vivo-Morpholino knockdown of alphaIIb: A novel approach to inhibit thrombocyte function in adult zebrafishSeongcheol Kim, Uvaraj P Radhakrishnan, Surendra Kumar Rajpurohit, et al.Blood Cells, Molecules & Diseases|November 29, 2005
Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infantM J Percy, L J Crowley, D Roper, et al.Blood Cells, Molecules & Diseases|November 3, 2009
A common SNP near BMP2 is associated with severity of the iron burden in HFE p.C282Y homozygous patients: a follow-up studyJacqueline Milet, Gérald Le Gac, Virginie Scotet, et al.Pageof 220