Showing results (111-120 of 122) with videos related to

Sort By:
Pageof 13
The Journal of Clinical Investigation|March 1, 1992
A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrinP G Gallagher, W T Tse, T Coetzer, et al.
Talanta|October 31, 2008
Speciation of selenite and selenate using living bacteriaL C Robles, J C Feo, B de Celis, et al.
Archives Francaises De Pediatrie|June 1, 1986
[Auto-immune hemolytic anemia revealed by erythroblastopenia linked to a parvovirus infection]Y Bertrand, J J Lefrère, G Leverger, et al.
The Journal of Clinical Investigation|January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosisP B Jenkins, G K Abou-Alfa, D Dhermy, et al.
British Journal of Haematology|October 1, 1996
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in BeninC Glele-Kakai, M Garbarz, M C Lecomte, et al.
American Journal of Hematology|July 1, 1988
Hemoglobin J Guantanamo [alpha 2 beta 2 128 (H6) Ala----Asp] in association with hemoglobin C and alpha-thalassemia in a family from BeninH Wajcman, V Baudin-Chich, J Kister, et al.
British Journal of Haematology|July 1, 1990
A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblingsA Ghanem, B Pothier, J Marechal, et al.
Water Research|January 6, 2007
Retention of inorganic arsenic by coryneform mutant strainsJ C Feo, E Ordoñez, M Letek, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|October 20, 2006
Colorectal cancer screening: results of a 5-year program in asymptomatic subjects at increased riskA Pezzoli, V Matarese, M Rubini, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPID Moatti, P Seknadji, C Galand, et al.
Pageof 13