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Human Genetics|January 1, 1980
Heterogeneity in beta 0 thalassemia from Algeria: genetic, clinical and molecular studiesM Belhani, F Morlé, P Colonna, et al.Blood|March 1, 1980
Mapping the alpha-globin genes in an Algerian HbH patient and his familyE Whitelaw, J Pagnier, G Verdier, et al.Biochimica Et Biophysica Acta|June 11, 1985
Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosisN Alloisio, L Morlé, D Bachir, et al.American Journal of Hematology|December 1, 1982
Kinetic alterations of the red cell membrane phosphatase in alpha- and beta-thalassemiaL Morlé, E Dorléac, N Alloisio, et al.The Journal of Biological Chemistry|November 15, 1989
A study of membrane protein defects and alpha hemoglobin chains of red blood cells in human beta thalassemiaP Rouyer-Fessard, M C Garel, C Domenget, et al.Journal of Cell Science|October 31, 2001
Podosomes in osteoclast-like cells: structural analysis and cooperative roles of paxillin, proline-rich tyrosine kinase 2 (Pyk2) and integrin alphaVbeta3M Pfaff, P JurdicBiochemical and Biophysical Research Communications|May 9, 2000
Differential regulation of the carbonic anhydrase II gene expression by hormonal nuclear receptors in monocytic cells: identification of the retinoic acid response elementI Quélo, P JurdicBlood|June 1, 1989
Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated familiesA F Roux, F Morlé, D Guetarni, et al.Blood|September 1, 1977
beta-O-thalassemia from Algeria: genetic and molecular characterizationJ Godet, G Verdier, V Nigon, et al.Biochemical and Biophysical Research Communications|October 19, 2001
RANKL induces formation of avian osteoclasts from macrophages but not from macrophage polykaryonsP Boissy, O Destaing, P JurdicPageof 29