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Seminars in Thrombosis and Hemostasis|January 1, 1996
Gene defects in congenital factor XIII deficiencyH Mikkola, A PalotieThrombosis and Haemostasis|June 1, 1997
Molecular mechanisms of mutations in factor XIII A-subunit deficiency: in vitro expression in COS-cells demonstrates intracellular degradation of the mutant proteinsH Mikkola, L Muszbek, G Haramura, et al.Blood|July 15, 1994
Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levelsH Mikkola, M Syrjälä, V Rasi, et al.Scandinavian Journal of Gastroenterology|April 7, 1999
Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel diseaseT Heliö, U Wartiovaara, L Halme, et al.Thrombosis and Haemostasis|November 1, 2000
Effect of Val34Leu polymorphism on the activation of the coagulation factor XIII-AU Wartiovaara, H Mikkola, G Szôke, et al.Blood|February 15, 1997
Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency: a splicing mutation permitting partial correct splicing of FXIII A-subunit mRNAH Mikkola, L Muszbek, E Laiho, et al.Collagen and Related Research|March 1, 1983
Effect of elevated temperature on the intracellular degradation of different collagen typesA PalotieAmerican Journal of Human Genetics|October 27, 1997
Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated populationE Laiho, J Ignatius, H Mikkola, et al.Blood|January 1, 1996
Four novel mutations in deficiency of coagulation factor XIII: consequences to expression and structure of the A-subunitH Mikkola, V C Yee, M Syrjälä, et al.Thrombosis and Haemostasis|July 31, 1998
Peripheral blood platelets express VEGF-C and VEGF which are released during platelet activationU Wartiovaara, P Salven, H Mikkola, et al.Pageof 17