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The Journal of Biological Chemistry|June 15, 1989
A novel amino acid substitution in the reactive site of a congenital variant antithrombin. Antithrombin pescara, ARG393 to pro, caused by a CGT to CCT mutationD A Lane, H Erdjument, E Thompson, et al.British Journal of Haematology|May 1, 1987
Thalassaemia intermedia: interaction of the triple alpha-globin gene arrangement and heterozygous beta-thalassaemiaA E Kulozik, S L Thein, J S Wainscoat, et al.Blood|December 23, 1999
Genetic influences on F cells and other hematologic variables: a twin heritability studyC Garner, T Tatu, J E Reittie, et al.Annals of the New York Academy of Sciences|July 21, 1998
Elimination of transfusions through induction of fetal hemoglobin synthesis in Cooley's anemiaN F Olivieri, D C Rees, G D Ginder, et al.Blood|December 15, 1994
Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch familiesH H van Boven, R J Olds, S L Thein, et al.Lancet (London, England)|October 4, 1986
First-trimester fetal diagnosis for haemoglobinopathies: report on 200 casesJ M Old, A Fitches, C Heath, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Molecular basis for dominantly inherited inclusion body beta-thalassemiaS L Thein, C Hesketh, P Taylor, et al.British Journal of Haematology|September 1, 1991
Antithrombin Glasgow II: alanine 382 to threonine mutation in the serpin P12 position, resulting in a substrate reaction with thrombinH Ireland, D A Lane, E Thompson, et al.Digestion|January 1, 1987
Time relationships between cessation of smoking and onset of ulcerative colitisR J Motley, J Rhodes, G A Ford, et al.British Journal of Haematology|January 1, 1991
Antithrombin Vicenza, Ala 384 to Pro (GCA to CCA) mutation, transforming the inhibitor into a substrateR Caso, D A Lane, E A Thompson, et al.Pageof 15