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Human Genetics|December 1, 1986
Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosisD Dhermy, M Garbarz, M C Lecomte, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1996
Human erythroid spectrin alpha subunit and its SH3 domain are sensitive to acidic Plasmodium falciparum proteolytic activityS L Le Bonniec, C Fournier, C Deregnaucourt, et al.Journal of Biochemical and Biophysical Methods|May 1, 1989
An efficient laboratory made apparatus for DNA amplificationO Bertrand, M H Delfau, M Garbarz, et al.Blood|May 1, 1985
A new abnormal variant of spectrin in black patients with hereditary elliptocytosisM C Lecomte, D Dhermy, C Solis, et al.The Journal of Cardiovascular Surgery|December 1, 1996
Membranous obstruction of the inferior vena cava and Budd-Chiari syndrome. Report of a caseP Zamboni, L Pisano, C Mari, et al.Analytical and Bioanalytical Chemistry|June 25, 2004
Fourier-transform infrared spectroscopic study of the interactions of selenium species with living bacterial cellsJ C Feo, M A Castro, L C Robles, et al.British Journal of Haematology|November 1, 1994
A variant of spectrin low-expression allele alpha LELY carrying a hereditary elliptocytosis mutation in codon 28J Randon, L Boulanger, J Marechal, et al.British Journal of Haematology|February 5, 1998
A 5' splice region G-->C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao)M Garbarz, C Galand, D Bibas, et al.Blood|July 1, 1994
Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact siteN Parquet, I Devaux, L Boulanger, et al.The Journal of Clinical Investigation|February 1, 1981
Separate mechanisms of deformability loss in ATP-depleted and Ca-loaded erythrocytesM R Clark, N Mohandas, C Feo, et al.Pageof 13