H. Mikkola

发表

Effect of Val34Leu Polymorphism on the Activation of the Coagulation Factor XIII-A

A. Palotie, R. Lassila, I. Balogh, 2000, Thrombosis and Haemostasis.

Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levels.

L. Peltonen, A. Palotie, E. Hämäläinen, 1994, Blood.

Association of a Common Polymorphism in the Factor XIII Gene with Myocardial Infarction

A. Carter, N. Ossei-Gerning, P. Grant, 1998, Thrombosis and Haemostasis.

Association of FXIII Val34Leu with decreased risk of myocardial infarction in Finnish males.

L. Peltonen, E. Vartiainen, M. Perola, 1999, Atherosclerosis.

Molecular Mechanisms of Mutations in Factor XIII A-subunit Deficiency: In vitro Expression in COS-cells Demonstrates Intracellular Degradation of the Mutant Proteins

A. Palotie, E. Hämäläinen, A. Jalanko, 1997, Thrombosis and Haemostasis.

Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency: a splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA.

L. Peltonen, A. Palotie, T. Salmi, 1997, Blood.

Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease.

A. Palotie, M. Färkkilä, T. Heliö, 1999, Scandinavian journal of gastroenterology.

Novel aspects of blood coagulation factor XIII. I. Structure, distribution, activation, and function.

R. Ádány, L. Muszbek, H. Mikkola, 1996, Critical reviews in clinical laboratory sciences.

Peripheral Blood Platelets Express VEGF-C and VEGF which Are Released during Platelet Activation

A. Palotie, K. Alitalo, H. Joensuu, 1998, Thrombosis and Haemostasis.

Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population.

J. Kere, A. Palotie, D. Teller, 1997, American journal of human genetics.

mutations demonstrate different effects on transcript levels Deficiency in the A-subunit of coagulation factor XIII: two novel point

L. Peltonen, A. Palotie, E. Hämäläinen, 2011 .

Four novel mutations in deficiency of coagulation factor XIII: consequences to expression and structure of the A-subunit.

L. Peltonen, A. Palotie, R. Ljung, 1996, Blood.

Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia.

I. Komáromi, É. Katona, I. Balogh, 2000, Blood.

Probiotic intervention decreases serum gastrin-17 in Helicobacter pylori infection.

R. Korpela, K. Kajander, H. Vapaatalo, 2007, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Gene Defects in Congenital Factor XIII Deficiency

A. Palotie, H. Mikkola, 1996, Seminars in thrombosis and hemostasis.