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 *

114 related articles for article (PubMed ID: 10607700)

  • 21. [Recurrent deep vein thrombosis caused by heterozygous missense mutation of the protein S gene: genetic analysis of a case].
    Ye X; Liu XL; Feng Y; Zhou XH; Xing ZF
    Nan Fang Yi Ke Da Xue Xue Bao; 2011 Jun; 31(7):1228-31. PubMed ID: 21764702
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Protein S deficiency type I: identification of point mutations in 9 of 10 families.
    Mustafa S; Pabinger I; Mannhalter C
    Blood; 1995 Nov; 86(9):3444-51. PubMed ID: 7579449
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 91(6):1105-14. PubMed ID: 15175796
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification of two different mutations causing protein S deficiency in two unrelated Belgian families using a nonisotopic scanning and sequencing method.
    Messiaen L; Callens T; Baele G
    Haemostasis; 1997; 27(5):228-36. PubMed ID: 9690481
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.
    Duga S; Asselta R; Santagostino E; Zeinali S; Simonic T; Malcovati M; Mannucci PM; Tenchini ML
    Blood; 2000 Feb; 95(4):1336-41. PubMed ID: 10666208
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study.
    Biguzzi E; Razzari C; Lane DA; Castaman G; Cappellari A; Bucciarelli P; Fontana G; Margaglione M; D'Andrea G; Simmonds RE; Rezende SM; Preston R; Prisco D; Faioni EM;
    Hum Mutat; 2005 Mar; 25(3):259-69. PubMed ID: 15712227
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Two distinct novel splice site mutations in a compound heterozygous patient with protein S deficiency.
    Yamazaki T; Katsumi A; Okamoto Y; Takafuta T; Tsuzuki S; Kagami K; Sugiura I; Kojima T; Fujimura K; Saito H
    Thromb Haemost; 1997 Jan; 77(1):14-20. PubMed ID: 9031442
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Compound heterozygous mutations identified in severe type I protein S deficiency impaired the secretion of protein S.
    Zhou J; Shen W; Gu Y; Li M; Shen W
    J Clin Pathol; 2020 Jan; 73(1):7-13. PubMed ID: 31422373
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Identification of protein Salpha gene mutations including four novel mutations in eight unrelated patients with protein S deficiency.
    Okada H; Takagi A; Murate T; Adachi T; Yamamoto K; Matsushita T; Takamatsu J; Sugita K; Sugimoto M; Yoshioka A; Yamazaki T; Saito H; Kojima T
    Br J Haematol; 2004 Jul; 126(2):219-25. PubMed ID: 15238143
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular basis of protein S deficiency in China.
    Tang L; Jian XR; Hamasaki N; Guo T; Wang HF; Lu X; Wang QY; Hu Y
    Am J Hematol; 2013 Oct; 88(10):899-905. PubMed ID: 23813890
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S.
    Makris M; Leach M; Beauchamp NJ; Daly ME; Cooper PC; Hampton KK; Bayliss P; Peake IR; Miller GJ; Preston FE
    Blood; 2000 Mar; 95(6):1935-41. PubMed ID: 10706858
    [TBL] [Abstract][Full Text] [Related]  

  • 32. One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.
    Mizukami K; Nakabayashi T; Naitoh S; Takeda M; Tarumi T; Mizoguchi I; Ieko M; Koike T
    Am J Hematol; 2006 Oct; 81(10):787-97. PubMed ID: 16868938
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.
    Borgel D; Duchemin J; Alhenc-Gelas M; Matheron C; Aiach M; Gandrille S
    J Lab Clin Med; 1996 Aug; 128(2):218-27. PubMed ID: 8765219
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes.
    Simmonds RE; Zöller B; Ireland H; Thompson E; de Frutos PG; Dahlbäck B; Lane DA
    Blood; 1997 Jun; 89(12):4364-70. PubMed ID: 9192759
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Factor V New Brunswick: Ala221Val associated with FV deficiency reproduced in vitro and functionally characterized.
    Steen M; Miteva M; Villoutreix BO; Yamazaki T; Dahlbäck B
    Blood; 2003 Aug; 102(4):1316-22. PubMed ID: 12714495
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Compound heterozygous mutations in the PROS1 gene responsible for quantitative and qualitative protein S deficiency.
    Yamanouchi J; Hato T; Tamura T; Fujiwara H; Yakushijin Y; Yasukawa M
    Int J Hematol; 2009 Nov; 90(4):537-539. PubMed ID: 19826897
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. Gly74Ser mutation in protein C causes thrombosis due to a defect in protein S-dependent anticoagulant function.
    Chen C; Yang L; Villoutreix BO; Wang X; Ding Q; Rezaie AR
    Thromb Haemost; 2017 Jun; 117(7):1358-1369. PubMed ID: 28405673
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy.
    Formstone CJ; Wacey AI; Berg LP; Rahman S; Bevan D; Rowley M; Voke J; Bernardi F; Legnani C; Simioni P; Girolami A; Tuddenham EG; Kakkar VV; Cooper DN
    Blood; 1995 Oct; 86(7):2632-41. PubMed ID: 7545463
    [TBL] [Abstract][Full Text] [Related]  

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