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See Latest ArticlesMolecular characterization of a novel mutation in the factor XIII a subunit gene associated with a severe defect: importance of prophylactic substitution
Blood Coagulation & Fibrinolysis, 10/07/09
Morange P et al. – Mutation gene analysis found a homozygous four bases insertion predicting a stop codon seven residues after PRO675. Antigen assay indicated that the mutant molecule is secreted. This case highlights the importance of prophylactic FXIII infusion.
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Today in Basic Science/Genetics...keeping you current
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Mutation analysis of the MSMB gene in familial prostate cancer
British Journal of Cancer, 12/10/09
Influence of omega-6 PUFA arachidonic acid and bone marrow adipocytes on metastatic spread from prostate cancer
British Journal of Cancer, 12/10/09
Gene set enrichment analysis provides insight into novel signalling pathways in breast cancer stem cells
British Journal of Cancer, 12/10/09
Today in Coagulation/Bleeding Dz...keeping you current
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Kasabach–Merritt phenomenon: a single centre experience
European Journal of Haematology, 12/10/09
Thrombotic thrombocytopenia purpura (TTP) and other thrombotic microangiopathies
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Developments in factor Xa inhibitors for the treatment of thromboembolic disorders
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