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Biomedical Science|January 1, 1991
Rat DNA sequence associated with a complex form of DNA polymerase alpha in nonregenerating liver interacts with a ubiquitous transcription/replication factor Oct-1N A Timchenko, O P Zhuchenko, L T Timchenko, et al.
Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Venous thromboembolism, oral contraceptives and high prothrombin levelsC Legnani, B Cosmi, L Valdrè, et al.
Human Molecular Genetics|May 1, 1993
In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand diseaseF Bernardi, P Patracchini, D Gemmati, et al.
British Journal of Haematology|December 19, 1998
Two novel mutations (Pro864His, Val867Glu) causing type 2A von Willebrand disease and affecting a single restriction site in exon 28F Bernardi, A Casonato, G Marchetti, et al.
Liver|August 1, 1992
Localization of cloned human DNA sequences and analysis of chromosomal alterations by in situ hybridizationP Patracchini, V Aiello, G Marchetti, et al.
Journal of Thrombosis and Haemostasis : JTH|October 1, 2008
Reduced factor VII and factor VIII levels and prolonged thrombin-generation times during a healthy diet in middle-aged women with mild to moderate cardiovascular disease riskA Passaro, S Calzavarini, S Volpato, et al.
Experimental Brain Research|March 22, 2013
Grasping in wonderland: altering the visual size of the body recalibrates the body schemaN F Bernardi, B F Marino, A Maravita, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 14, 2001
The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot studyC Incorvaia, F Parmeggiani, C Costagliola, et al.
Thrombosis and Haemostasis|December 20, 1993
Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assayE M Faioni, F Franchi, D Asti, et al.
Haematologica|June 22, 2001
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian populationE Castoldi, B Lunghi, F Mingozzi, et al.
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