These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 8822580)

  • 21. 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; 125(5):647-54. PubMed ID: 15147381
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency.
    Pung-amritt P; Poort SR; Vos HL; Bertina RM; Mahasandana C; Tanphaichitr VS; Veerakul G; Kankirawatana S; Suvatte V
    Thromb Haemost; 1999 Feb; 81(2):189-92. PubMed ID: 10063989
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Ser 460 to Pro substitution of the protein S alpha (PROS1) gene is a frequent mutation associated with free protein S (type IIa) deficiency.
    Duchemin J; Gandrille S; Borgel D; Feurgard P; Alhenc-Gelas M; Matheron C; Dreyfus M; Dupuy E; Juhan-Vague I; Aiach M
    Blood; 1995 Nov; 86(9):3436-43. PubMed ID: 7579448
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement.
    Alhenc Gelas M; Juin F; de Raucourt E; Gandrille S; Borgel D; Aiach M
    Thromb Haemost; 2007 Apr; 97(4):678-80. PubMed ID: 17393035
    [No Abstract]   [Full Text] [Related]  

  • 25. DNA sequence analysis of protein S deficiency--identification of four point mutations in twelve Japanese subjects.
    Iwaki T; Mastushita T; Kobayashi T; Yamamoto Y; Nomura Y; Kagami K; Nakayama T; Sugiura I; Kojima T; Takamatsu J; Kanayama N; Saito H
    Semin Thromb Hemost; 2001; 27(2):155-60. PubMed ID: 11372770
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An Sp1 binding site mutation of the PROS1 promoter in a patient with protein S deficiency.
    Sanda N; Fujimori Y; Kashiwagi T; Takagi A; Murate T; Mizutani E; Matsushita T; Naoe T; Kojima T
    Br J Haematol; 2007 Sep; 138(5):663-5. PubMed ID: 17596203
    [No Abstract]   [Full Text] [Related]  

  • 27. Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
    Boinot C; Borgel D; Kitzis A; Guicheteau M; Aiach M; Alhenc-Gelas M
    Blood Coagul Fibrinolysis; 2003 Feb; 14(2):191-6. PubMed ID: 12632031
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Protein S Thr103Asn mutation associated with type II deficiency reproduced in vitro and functionally characterised.
    Giri TK; García de Frutos P; Dahlbäck B
    Thromb Haemost; 2000 Sep; 84(3):413-9. PubMed ID: 11019964
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Confirmation of inherited protein S deficiency by PROS1 mutational screening: Identification of three novel PROS1 mutations and haplotype analysis of p.Q279X recurrence.
    Hurtado B; Abasolo N; Domènech-Santasusana P; Fuentes-Prior P; García de Frutos P; Sala N
    Thromb Haemost; 2008 Oct; 100(4):721-4. PubMed ID: 18841302
    [No Abstract]   [Full Text] [Related]  

  • 30. Genetic modulation of plasma protein S levels by two frequent dimorphisms in the PROS1 gene.
    Leroy-Matheron C; Duchemin J; Levent M; Gouault-Heilmann M
    Thromb Haemost; 1999 Sep; 82(3):1088-92. PubMed ID: 10494768
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Large deletions of the PROS1 gene in a large fraction of mutation-negative patients with protein S deficiency.
    Johansson AM; Hillarp A; Säll T; Zöller B; Dahlbäck B; Halldén C
    Thromb Haemost; 2005 Nov; 94(5):951-7. PubMed ID: 16363235
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Protein C and protein S assessment in hospital laboratories: which strategy and what role for DNA sequencing?
    Labrouche S; Reboul MP; Guérin V; Vergnes C; Freyburger G
    Blood Coagul Fibrinolysis; 2003 Sep; 14(6):531-8. PubMed ID: 12960605
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Protein C and protein S deficiencies.
    Aiach M; Borgel D; Gaussem P; Emmerich J; Alhenc-Gelas M; Gandrille S
    Semin Hematol; 1997 Jul; 34(3):205-16. PubMed ID: 9241706
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [A point mutation of protein C gene in a congenital protein C deficiency pedigree].
    Liu L; Guo WR; He LS; Mu H; Jiang Y; Huang FQ; Li JZ
    Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):115-8. PubMed ID: 12697119
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel splice acceptor site mutation which produces multiple splicing abnormalities resulting in protein S deficiency type I.
    Tatewaki H; Iida H; Nakahara M; Tsuda H; Kinoshita S; Kanaji T; Yoshida N; Miyazaki S; Hamasaki N
    Thromb Haemost; 1999 Jul; 82(1):65-71. PubMed ID: 10456456
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Gene symbol: PROS1. Disease: Protein S deficiency.
    Steidle M; Pfanner G; Haug B
    Hum Genet; 2008 Oct; 124(3):313. PubMed ID: 18846658
    [No Abstract]   [Full Text] [Related]  

  • 37. Gene symbol: PROS1. Disease: Protein S deficiency.
    Steidle M; Pfanner G; Haug B
    Hum Genet; 2008 Oct; 124(3):316. PubMed ID: 18846666
    [No Abstract]   [Full Text] [Related]  

  • 38. A novel mutation in intron K of the PROS1 gene causes aberrant RNA splicing and is a common cause of protein S deficiency in a UK thrombophilia cohort.
    Beauchamp NJ; Daly ME; Makris M; Preston FE; Peake IR
    Thromb Haemost; 1998 Jun; 79(6):1086-91. PubMed ID: 9657428
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Type I protein C deficiency caused by a novel protein C gene mutation].
    Zheng Y; Zhu D; Zhou B
    Zhonghua Xue Ye Xue Za Zhi; 1998 Mar; 19(3):138-42. PubMed ID: 11243145
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
    Zhou RF; Fu QH; Wang WB; Xie S; Hu YQ; Wang XF; Wang ZY; Wang HL
    Chin Med J (Engl); 2004 Jun; 117(6):813-7. PubMed ID: 15198878
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.