H K Ploos van Amstel - JoVE Visualize

Showing results (1-10 of 26) with videos related to

Pageof 3

Sort By:

Biochemical and Biophysical Research Communications|December 30, 1988

The human protein S locus: identification of the PS alpha gene as a site of liver protein S messenger RNA synthesisH K Ploos van Amstel, P H Reitsma, R M Bertina

The Journal of Clinical Investigation|February 1, 1994

Three novel mutations in five unrelated subjects with hereditary protein S deficiency type IP H Reitsma, H K Ploos van Amstel, R M Bertina

Thrombosis and Haemostasis|October 5, 1992

Mutations in severe, type III von Willebrand's disease in the Dutch population: candidate missense and nonsense mutations associated with reduced levels of von Willebrand factor messenger RNAJ C Eikenboom, H K Ploos van Amstel, P H Reitsma, et al.

Biochemistry|August 28, 1990

Intron-exon organization of the active human protein S gene PS alpha and its pseudogene PS beta: duplication and silencing during primate evolutionH K Ploos van Amstel, P H Reitsma, C P van der Logt, et al.

FEBS Letters|September 28, 1987

Human protein S cDNA encodes Phe-16 and Tyr 222 in consensus sequences for the post-translational processingH K Ploos van Amstel, A L van der Zanden, P H Reitsma, et al.

Prenatal Diagnosis|November 14, 1997

Mutation analysis for prenatal diagnosis of hereditary tyrosinaemia type 1A Mustonen, H K Ploos van Amstel, R Berger, et al.

Blood|February 1, 1989

Partial protein S gene deletion in a family with hereditary thrombophiliaH K Ploos van Amstel, M V Huisman, P H Reitsma, et al.

Thrombosis and Haemostasis|May 4, 1992

Expression and characterization of recombinant human protein S in heterologous cells--studies of the interaction of amino acid residues leu-608 to glu-612 with human C4b-binding proteinG T Chang, H K Ploos van Amstel, M Hessing, et al.

Neurology|March 17, 1999

A diagnostic protocol for adult-onset glycogen storage disease type IIM G Ausems, P Lochman, O P van Diggelen, et al.

Thrombosis and Haemostasis|April 1, 1994

Studies of the interaction between human protein S and human C4b-binding protein using deletion variants of recombinant human protein SG T Chang, B H Maas, H K Ploos van Amstel, et al.

Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:

Pageof 3

Biochemical and Biophysical Research Communications|December 30, 1988

The human protein S locus: identification of the PS alpha gene as a site of liver protein S messenger RNA synthesisH K Ploos van Amstel, P H Reitsma, R M Bertina

The Journal of Clinical Investigation|February 1, 1994

Three novel mutations in five unrelated subjects with hereditary protein S deficiency type IP H Reitsma, H K Ploos van Amstel, R M Bertina

Thrombosis and Haemostasis|October 5, 1992

Mutations in severe, type III von Willebrand's disease in the Dutch population: candidate missense and nonsense mutations associated with reduced levels of von Willebrand factor messenger RNAJ C Eikenboom, H K Ploos van Amstel, P H Reitsma, et al.

Biochemistry|August 28, 1990

Intron-exon organization of the active human protein S gene PS alpha and its pseudogene PS beta: duplication and silencing during primate evolutionH K Ploos van Amstel, P H Reitsma, C P van der Logt, et al.

FEBS Letters|September 28, 1987

Human protein S cDNA encodes Phe-16 and Tyr 222 in consensus sequences for the post-translational processingH K Ploos van Amstel, A L van der Zanden, P H Reitsma, et al.

Prenatal Diagnosis|November 14, 1997

Mutation analysis for prenatal diagnosis of hereditary tyrosinaemia type 1A Mustonen, H K Ploos van Amstel, R Berger, et al.

Blood|February 1, 1989

Partial protein S gene deletion in a family with hereditary thrombophiliaH K Ploos van Amstel, M V Huisman, P H Reitsma, et al.

Thrombosis and Haemostasis|May 4, 1992

Expression and characterization of recombinant human protein S in heterologous cells--studies of the interaction of amino acid residues leu-608 to glu-612 with human C4b-binding proteinG T Chang, H K Ploos van Amstel, M Hessing, et al.

Neurology|March 17, 1999

A diagnostic protocol for adult-onset glycogen storage disease type IIM G Ausems, P Lochman, O P van Diggelen, et al.

Thrombosis and Haemostasis|April 1, 1994

Studies of the interaction between human protein S and human C4b-binding protein using deletion variants of recombinant human protein SG T Chang, B H Maas, H K Ploos van Amstel, et al.

Pageof 3