Ploos van Amstel HK - Search Results

1

Rapid detection of genomic imbalances using micro-arrays consisting of pooled BACs covering all human chromosome arms.

Knijnenburg J, van der Burg M, Nilsson P, Ploos van Amstel HK, Tanke H, Szuhai K. Knijnenburg J, et al. Among authors: ploos van amstel hk, van der burg m. Nucleic Acids Res. 2005 Oct 12;33(18):e159. doi: 10.1093/nar/gni161. Nucleic Acids Res. 2005. PMID: 16221972 Free PMC article.

2

RFLP for the human prothrombin (F2) gene.

de Vetten M, Ploos van Amstel HK, Reitsma PH. de Vetten M, et al. Among authors: ploos van amstel hk. Nucleic Acids Res. 1990 Oct 11;18(19):5917. doi: 10.1093/nar/18.19.5917. Nucleic Acids Res. 1990. PMID: 1977138 Free PMC article.

3

Intron-exon organization of the active human protein S gene PS alpha and its pseudogene PS beta: duplication and silencing during primate evolution.

Ploos van Amstel HK, Reitsma PH, van der Logt CP, Bertina RM. Ploos van Amstel HK, et al. Among authors: van der logt cp. Biochemistry. 1990 Aug 28;29(34):7853-61. doi: 10.1021/bi00486a011. Biochemistry. 1990. PMID: 2148111

4

Partial protein S gene deletion in a family with hereditary thrombophilia.

Ploos van Amstel HK, Huisman MV, Reitsma PH, Wouter ten Cate J, Bertina RM. Ploos van Amstel HK, et al. Blood. 1989 Feb;73(2):479-83. Blood. 1989. PMID: 2521801 Free article.

5

Human protein S cDNA encodes Phe-16 and Tyr 222 in consensus sequences for the post-translational processing.

Ploos van Amstel HK, van der Zanden AL, Reitsma PH, Bertina RM. Ploos van Amstel HK, et al. Among authors: van der zanden al. FEBS Lett. 1987 Sep 28;222(1):186-90. doi: 10.1016/0014-5793(87)80217-x. FEBS Lett. 1987. PMID: 2820795 Free article.

6

The human protein S locus: identification of the PS alpha gene as a site of liver protein S messenger RNA synthesis.

Ploos van Amstel HK, Reitsma PH, Bertina RM. Ploos van Amstel HK, et al. Biochem Biophys Res Commun. 1988 Dec 30;157(3):1033-8. doi: 10.1016/s0006-291x(88)80978-1. Biochem Biophys Res Commun. 1988. PMID: 2974696

7

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 RNA.

Eikenboom JC, Ploos van Amstel HK, Reitsma PH, Briët E. Eikenboom JC, et al. Among authors: ploos van amstel hk. Thromb Haemost. 1992 Oct 5;68(4):448-54. Thromb Haemost. 1992. PMID: 1448779

8

Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460.

Bertina RM, Ploos van Amstel HK, van Wijngaarden A, Coenen J, Leemhuis MP, Deutz-Terlouw PP, van der Linden IK, Reitsma PH. Bertina RM, et al. Among authors: van der linden ik, ploos van amstel hk, van wijngaarden a. Blood. 1990 Aug 1;76(3):538-48. Blood. 1990. PMID: 2143091 Free article.

9

A mutation in the protein S pseudogene is linked to protein S deficiency in a thrombophilic family.

Ploos van Amstel HK, Reitsma PH, Hamulyák K, de Die-Smulders CE, Mannucci PM, Bertina RM. Ploos van Amstel HK, et al. Thromb Haemost. 1989 Nov 24;62(3):897-901. Thromb Haemost. 1989. PMID: 2531940

10

Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I.

Reitsma PH, Ploos van Amstel HK, Bertina RM. Reitsma PH, et al. Among authors: ploos van amstel hk. J Clin Invest. 1994 Feb;93(2):486-92. doi: 10.1172/JCI116997. J Clin Invest. 1994. PMID: 8113388 Free PMC article.

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