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Items where Author is "Rezende, S"

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Number of items: 8.


Biguzzi, E, Razzari, C, Lane, DA, Castaman, G, Cappellari, A, Bucciarelli, P, Fontana, G, Margaglione, M, D'Andrea, G, Simmonds, RE, Rezende, SM, Preston, R, Prisco, D and Faioni, EM (2005) Molecular diversity and thrombotic risk in Protein S deficiency: The PROSIT study HUMAN MUTATION, 25 (3). pp. 259-269.

Rezende, SM, Simmonds, RE and Lane, DA (2004) Coagulation, inflammation, and apoptosis: different roles for protein S and the protein S-C4b binding protein complex BLOOD, 103 (4). pp. 1192-1201.

Mille-Baker, B, Rezende, SM, Simmonds, RE, Mason, PJ, Lane, DA and Laffan, MA (2003) Deletion or replacement of the second EGF-hke domain of protein S results in loss of APC cofactor activity BLOOD, 101 (4). pp. 1416-1418.

Rezende, SM, Lane, DA, Mille-Baker, B, Samama, MM, Conard, J and Simmonds, RE (2002) Protein S Gla-domain mutations causing impaired Ca2+-induced phospholipid binding and severe functional protein S deficiency BLOOD, 100 (8). pp. 2812-2819.

Rezende, SM, Lane, DA, Zoller, B, Mille-Baker, B, Laffan, M, Dahlback, B and Simmonds, RE (2002) Genetic and phenotypic variability between families with hereditary protein S deficiency THROMBOSIS AND HAEMOSTASIS, 87 (2). pp. 258-265.

Gandrille, S, Borgel, D, Sala, N, Espinosa-Parrilla, Y, Simmonds, R, Rezende, S, Lind, B, Mannhalter, C, Pabinger, I, Reitsma, PH, Formstone, C, Cooper, DN, Saito, H, Suzuki, K, Bernardi, F and Aiach, M (2000) Protein S deficiency: A database of mutations - Summary of the first update THROMBOSIS AND HAEMOSTASIS, 84 (5). p. 918.

Rezende, SM, Simmonds, RE, Zoller, B, Dahlback, B and Lane, DA (1999) The molecular basis of type I/III protein S deficiency THROMBOSIS AND HAEMOSTASIS. pp. 426-427.

Conference or Workshop Item

Simmonds, RE, Hermida, J, Rezende, SM and Lane, DA (2001) Haemostatic genetic risk factors in arterial thrombosis In: XVIIIth Congress of the International-Society-on-Thrombosis-and-Haemostasis, 2001-07-06 - 2001-07-12, PARIS, FRANCE.

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