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H L Vos

Showing results (11-20 of 58) with videos related to

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Nucleic Acids Research|January 25, 1991
A single nucleotide polymorphism in an exon dictates allele dependent differential splicing of episialin mRNAM J Ligtenberg, A M Gennissen, H L Vos, et al.
Journal of Thrombosis and Haemostasis : JTH|October 25, 2006
The association of prothrombin A19911G polymorphism with plasma prothrombin activity and venous thrombosis: results of the MEGA study, a large population-based case-control studyY Chinthammitr, H L Vos, F R Rosendaal, et al.
Virus Genes|June 1, 1990
Physical mapping of two temperature-sensitive adenovirus mutants affected in the DNA polymerase and DNA binding proteinD J Roovers, C S Young, H L Vos, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 16, 1999
Two novel mutations in the prothrombin gene cause severe bleeding in a compound heterozygous patientS R Poort, K T Njo, H L Vos, et al.
Thrombosis and Haemostasis|May 6, 1998
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian originJ C Eikenboom, G Castaman, H L Vos, et al.
Current Genetics|November 2, 2013
RNA processing in yeast mitochondria: characterization of mit(-) mutants disturbed in the synthesis of subunit I of cytochrome c oxidaseL A Hensgens, G van der Horst, H L Vos, et al.
Journal of Thrombosis and Haemostasis : JTH|January 14, 2004
G20210A is a functional mutation in the prothrombin gene; effect on protein levels and 3'-end formationH Ceelie, C C Spaargaren-van Riel, R M Bertina, et al.
The Journal of Cell Biology|April 1, 1995
Episialin (MUC1) overexpression inhibits integrin-mediated cell adhesion to extracellular matrix componentsJ Wesseling, S W van der Valk, H L Vos, et al.
British Journal of Haematology|April 29, 2006
Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand diseaseP Tjernberg, G Castaman, H L Vos, et al.
Journal of Thrombosis and Haemostasis : JTH|March 6, 2004
Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residuesP Tjernberg, H L Vos, G Castaman, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Nucleic Acids Research|January 25, 1991
A single nucleotide polymorphism in an exon dictates allele dependent differential splicing of episialin mRNAM J Ligtenberg, A M Gennissen, H L Vos, et al.
Journal of Thrombosis and Haemostasis : JTH|October 25, 2006
The association of prothrombin A19911G polymorphism with plasma prothrombin activity and venous thrombosis: results of the MEGA study, a large population-based case-control studyY Chinthammitr, H L Vos, F R Rosendaal, et al.
Virus Genes|June 1, 1990
Physical mapping of two temperature-sensitive adenovirus mutants affected in the DNA polymerase and DNA binding proteinD J Roovers, C S Young, H L Vos, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 16, 1999
Two novel mutations in the prothrombin gene cause severe bleeding in a compound heterozygous patientS R Poort, K T Njo, H L Vos, et al.
Thrombosis and Haemostasis|May 6, 1998
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian originJ C Eikenboom, G Castaman, H L Vos, et al.
Current Genetics|November 2, 2013
RNA processing in yeast mitochondria: characterization of mit(-) mutants disturbed in the synthesis of subunit I of cytochrome c oxidaseL A Hensgens, G van der Horst, H L Vos, et al.
Journal of Thrombosis and Haemostasis : JTH|January 14, 2004
G20210A is a functional mutation in the prothrombin gene; effect on protein levels and 3'-end formationH Ceelie, C C Spaargaren-van Riel, R M Bertina, et al.
The Journal of Cell Biology|April 1, 1995
Episialin (MUC1) overexpression inhibits integrin-mediated cell adhesion to extracellular matrix componentsJ Wesseling, S W van der Valk, H L Vos, et al.
British Journal of Haematology|April 29, 2006
Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand diseaseP Tjernberg, G Castaman, H L Vos, et al.
Journal of Thrombosis and Haemostasis : JTH|March 6, 2004
Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residuesP Tjernberg, H L Vos, G Castaman, et al.
Pageof 6