Zobrazeno 1 - 9
of 9
pro vyhledávání: '"HK Ploos van Amstel"'
Publikováno v:
Arthritis & Rheumatism. Oct2003, Vol. 48 Issue 10, p2995. 1p.
Publikováno v:
Journal of Clinical Investigation. 93:486-492
A panel of eight unrelated subjects with inherited type I protein S deficiency was screened for mutations in the PROS1 gene. In five subjects an abnormality was found but mutations were not detected in the remaining three subjects. Two subjects share
Autor:
B. H. A. Maas, Pieter H. Reitsma, Bonno N. Bouma, HK Ploos van Amstel, R M Bertina, Glenn T G Chang
Publikováno v:
Thrombosis and Haemostasis. 71:461-467
SummaryHuman protein S interacts noncovalently with human C4b-binding protein (C4BP). We have studied this interaction using deletion variants of recombinant human protein S. Two deletion variants were constructed by restriction enzyme digestion and
Autor:
RM Bertina, HK Ploos van Amstel, A van Wijngaarden, J Coenen, MP Leemhuis, PP Deutz-Terlouw, IK van der Linden, PH Reitsma
Publikováno v:
Blood. 76:538-548
We recently developed an enzyme-linked immunosorbent assay (ELISA) for total protein S (PS) antigen using the monoclonal antibody S-12. During the screening of thrombophilic patients we identified a patient, who was using marcoumar, with 0% PS by mon
Autor:
HK Ploos van Amstel, Piëtte P. Deutz-Terlouw, J Coenen, Pieter H. Reitsma, R M Bertina, MP Leemhuis, I K van der Linden, A van Wijngaarden
Publikováno v:
Blood. 76:538-548
We recently developed an enzyme-linked immunosorbent assay (ELISA) for total protein S (PS) antigen using the monoclonal antibody S-12. During the screening of thrombophilic patients we identified a patient, who was using marcoumar, with 0% PS by mon
Publikováno v:
Blood. 73:479-483
Familial thrombophilia, the hereditary predisposition to venous thromboembolic disease, is associated with a protein S deficiency in approximately 8% of the cases. Laboratory measurements of total protein S antigen in affected families have indicated
Autor:
Laan SNJ; Department of Internal Medicine, Division of Thrombosis and Hemostasis, Leiden University Medical Centre, Leiden, the Netherlands; Department of Hematology, Erasmus University Medical Centre, Rotterdam, the Netherlands. Electronic address: https://twitter.com/laan_bas., de Boer S; Department of Internal Medicine, Division of Thrombosis and Hemostasis, Leiden University Medical Centre, Leiden, the Netherlands., Dirven RJ; Department of Internal Medicine, Division of Thrombosis and Hemostasis, Leiden University Medical Centre, Leiden, the Netherlands., van Moort I; Department of Hematology, Erasmus University Medical Centre, Rotterdam, the Netherlands., Kuipers TB; Sequencing Analysis Support Core, Department of Biomedical Data Sciences, Leiden University Medical Centre, Leiden, the Netherlands., Mei H; Sequencing Analysis Support Core, Department of Biomedical Data Sciences, Leiden University Medical Centre, Leiden, the Netherlands., Bierings R; Department of Hematology, Erasmus University Medical Centre, Rotterdam, the Netherlands., Eikenboom J; Department of Internal Medicine, Division of Thrombosis and Hemostasis, Leiden University Medical Centre, Leiden, the Netherlands. Electronic address: h.c.j.eikenboom@lumc.nl.
Publikováno v:
Journal of thrombosis and haemostasis : JTH [J Thromb Haemost] 2024 Jul; Vol. 22 (7), pp. 2027-2038. Date of Electronic Publication: 2024 Apr 02.
Publikováno v:
Journal of Inherited Metabolic Disease; Nov2002, Vol. 25 Issue 6, p514-514, 1p
Publikováno v:
Seminars in Thrombosis & Hemostasis; 1995, Vol. 21 Issue 3, p261-275, 15p