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 *

100 related articles for article (PubMed ID: 10589087)

  • 1. A novel mutation of the protein C gene with a frameshift deletion of 3 base pair F ((3380)AGG) in exon 6 in type 1 deficiency associated with arterial and venous thrombosis.
    Takahashi T; Shinohara K; Nawata R; Wakiyama M; Hamasaki N
    Am J Hematol; 1999 Dec; 62(4):260-1. PubMed ID: 10589087
    [No Abstract]   [Full Text] [Related]  

  • 2. Hereditary basis of protein C deficiency (PCD) in thrombosis patients: first report from India.
    Pai N; Shetty S; Idicula-Thomas S; Kulkarni B; Ghosh K
    Thromb Haemost; 2009 Apr; 101(4):785-7. PubMed ID: 19350130
    [No Abstract]   [Full Text] [Related]  

  • 3. Identification of one base deletion in exon IX of the protein C gene that causes a type I deficiency.
    Tokunaga F; Wakabayashi S; Sato H; Arakawa M; Tawaraya H; Koide T
    Thromb Res; 1992 Dec; 68(4-5):417-23. PubMed ID: 1290170
    [No Abstract]   [Full Text] [Related]  

  • 4. A novel frameshift mutation Gly239Serfs*8 in the PROC gene results in protein C deficiency in a Korean patient.
    Park SH; Jang S; Yang HK; Shim H; Park CJ; Chi HS; Oh YM
    Ann Hematol; 2012 Nov; 91(11):1829-30. PubMed ID: 22588326
    [No Abstract]   [Full Text] [Related]  

  • 5. Identification of mutations in 15 Hungarian families with hereditary protein C deficiency.
    Dávid M; Losonczy H; Sas G; Nagy A; Kutscher G; Meyer M
    Br J Haematol; 2000 Oct; 111(1):129-35. PubMed ID: 11091192
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Acroangiodermatitis of Mali in protein C deficiency due to a novel PROC gene mutation.
    Wei-Min Tan A; Lee JS; Pramono ZA; Chong WS
    Am J Dermatopathol; 2012 Apr; 34(2):e19-21. PubMed ID: 22441373
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis.
    Millar DS; Grundy CB; Bignell P; Moffat EH; Martin R; Kakkar VV; Cooper DN
    Blood Coagul Fibrinolysis; 1993 Apr; 4(2):345-7. PubMed ID: 8499568
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiency.
    Hasstedt SJ; Bovill EG; Callas PW; Long GL
    Am J Hum Genet; 1998 Aug; 63(2):569-76. PubMed ID: 9683579
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A single base-pair deletion in the protein C gene causing recurrent thromboembolism.
    Grundy C; Plendl H; Grote W; Zoll B; Kakkar VV; Cooper DN
    Thromb Res; 1991 Feb; 61(3):335-40. PubMed ID: 2028449
    [No Abstract]   [Full Text] [Related]  

  • 10. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.
    Ireland H; Thompson E; Lane DA
    Thromb Haemost; 1996 Dec; 76(6):867-73. PubMed ID: 8972002
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Exclusion of the alpha2 subunit of platelet-activating factor acetylhydrolase 1b (PAFAH1B2) as a prothrombotic gene in a protein C-deficient kindred and population-based case-control sample.
    Hasstedt SJ; Scott BT; Rosendaal FR; Callas PW; Vossen CY; Long GL; Bovill EG
    Thromb Haemost; 2007 Sep; 98(3):587-92. PubMed ID: 17849047
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis-prone lineage.
    Bernardi F; Patracchini P; Gemmati D; Boninsegna S; Guerra S; Legnani C; Ballerini G; Marchetti G
    Br J Haematol; 1992 Jun; 81(2):277-82. PubMed ID: 1643025
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 76(2):143-50. PubMed ID: 8865520
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients.
    Altinisik J; Ates O; Ulutin T; Cengiz M; Buyru N
    Clin Appl Thromb Hemost; 2008 Oct; 14(4):415-20. PubMed ID: 18160601
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic analysis of a large kindred exhibiting type I protein C deficiency and associated thrombosis.
    Tomczak JA; Ando RA; Sobel HG; Bovill EG; Long GL
    Thromb Res; 1994 May; 74(3):243-54. PubMed ID: 7913773
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe arterial thrombosis in a family with type III protein S deficiency caused by a frameshift mutation in the PROS1 gene.
    Larsen TB; Brusgaard K; Nybo M
    Thromb Res; 2010 Aug; 126(2):e159-61. PubMed ID: 20398916
    [No Abstract]   [Full Text] [Related]  

  • 17. Acceptor splice site mutation in the invariant AG of intron 5 of the protein C gene, causing type I protein C deficiency.
    Soria JM; Fontcuberta J; Chillón M; Borrell M; Estivill X; Sala N
    Hum Genet; 1993 Nov; 92(5):506-8. PubMed ID: 8244342
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Protein C/S ratio, an accurate and simple tool to identify carriers of a protein C gene mutation.
    Libourel EJ; Meinardi JR; de Kam PJ; Veenstra R; van der Schaaf W; Ruiters MH; van der Meer J
    Br J Haematol; 2002 Aug; 118(2):615-8. PubMed ID: 12139756
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Protein C deficiency and venous thrombosis--the search for the second genetic defect.
    Bertina RM
    Thromb Haemost; 2000 Mar; 83(3):360-1. PubMed ID: 10744137
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.