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Journal Abstract Search

121 related items for PubMed ID: 2143091

  • 1. 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.
    Blood; 1990 Aug 01; 76(3):538-48. PubMed ID: 2143091
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  • 3. Deficient APC-cofactor activity of protein S Heerlen in degradation of factor Va Leiden: a possible mechanism of synergism between thrombophilic risk factors.
    Giri TK, Yamazaki T, Sala N, Dahlbäck B, de Frutos PG.
    Blood; 2000 Jul 15; 96(2):523-31. PubMed ID: 10887114
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  • 4. Direct anticoagulant activity of protein S-C4b binding protein complex in Heerlen heterozygotes and normals.
    Heeb MJ, Koenen RR, Fernández JA, Hackeng TM.
    J Thromb Haemost; 2004 Oct 15; 2(10):1766-73. PubMed ID: 15456488
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  • 5. Homozygosity for the protein S Heerlen allele is associated with type I PS deficiency in a thrombophilic pedigree with multiple risk factors.
    Espinosa-Parrilla Y, Navarro G, Morell M, Abella E, Estivill X, Sala N.
    Thromb Haemost; 2000 Jan 15; 83(1):102-6. PubMed ID: 10669162
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  • 6. Expression and characterization of recombinant protein S with the Ser 460 Pro mutation.
    Morboeuf O, Borgel D, Aiach M, Kaabache T, Gandrille S, Gaussem P.
    Thromb Res; 2000 Oct 01; 100(1):81-8. PubMed ID: 11053620
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  • 7. The Ser460Pro mutation in recombinant protein S Heerlen does not affect its APC-cofactor and APC-independent anticoagulant activities.
    Koenen RR, Gomes L, Tans G, Rosing J, Hackeng TM.
    Thromb Haemost; 2004 Jun 01; 91(6):1105-14. PubMed ID: 15175796
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  • 8. The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population.
    Beauchamp NJ, Dykes AC, Parikh N, Campbell Tait R, Daly ME.
    Br J Haematol; 2004 Jun 01; 125(5):647-54. PubMed ID: 15147381
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  • 10. A Case of a Pediatric Patient With Protein S Heerlen Polymorphism and Deep Venous Thrombosis.
    Kacar M, Bhatt M.
    J Pediatr Hematol Oncol; 2022 Mar 01; 44(2):e442-e443. PubMed ID: 34486549
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  • 11. The effect of N-linked glycosylation on molecular weight, thrombin cleavage, and functional activity of human protein S.
    Lu D, Xie RL, Rydzewski A, Long GL.
    Thromb Haemost; 1997 Jun 01; 77(6):1156-63. PubMed ID: 9241750
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  • 13. Monoclonal antibody-based enzyme-linked immunosorbent assays (ELISA) for the measurement of vitamin K-dependent protein S: the effect of antibody immunoreactivity on plasma protein S antigen determinations.
    D'Angelo SV, Tombesi S, Marcovina S, Albertini A, Della Valle P, D'Angelo A.
    Thromb Haemost; 1992 Jun 01; 67(6):631-8. PubMed ID: 1387263
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  • 15. Two mutations in exon XII of the protein S alpha gene in four thrombophilic families resulting in premature stop codons and depressed levels of mutated mRNA.
    Andersen BD, Lind B, Philips M, Hansen AB, Ingerslev J, Thorsen S.
    Thromb Haemost; 1996 Aug 01; 76(2):143-50. PubMed ID: 8865520
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  • 16. A phenotypically neutral dimorphism of protein S: the substitution of Lys155 by Glu in the second EGF domain predicted by an A to G base exchange in the gene.
    Yamazaki T, Sugiura I, Matsushita T, Kojima T, Kagami K, Takamatsu J, Saito H.
    Thromb Res; 1993 Jun 01; 70(5):395-403. PubMed ID: 8378895
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  • 18. Two distinct compound heterozygous constellations (R277X/IVS34-1G>C and R277X/R1511X) in the thyroglobulin (TG) gene in affected individuals of a Brazilian kindred with congenital goiter and defective TG synthesis.
    Gutnisky VJ, Moya CM, Rivolta CM, Domené S, Varela V, Toniolo JV, Medeiros-Neto G, Targovnik HM.
    J Clin Endocrinol Metab; 2004 Feb 01; 89(2):646-57. PubMed ID: 14764776
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