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 *

122 related articles for article (PubMed ID: 17002658)

  • 21. Molecular diagnosis of hypophosphatasia with severe periodontitis.
    Watanabe H; Goseki-Sone M; Iimura T; Oida S; Orimo H; Ishikawa I
    J Periodontol; 1999 Jun; 70(6):688-91. PubMed ID: 10397525
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion.
    Hewitt J; Ballard JN; Nelson TN; Smith VC; Griffiths TA; Pritchard S; Wu JK; Wadsworth LD; Casey B; MacGillivray RT
    Br J Haematol; 2005 Feb; 128(3):380-5. PubMed ID: 15667541
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency.
    Kuijper PH; Schellings MW; van de Kerkhof D; Nicolaes GA; Reitsma P; Halbertsma F; Dors N
    Haemophilia; 2013 Sep; 19(5):e304-6. PubMed ID: 23711336
    [No Abstract]   [Full Text] [Related]  

  • 24. Prothrombin deficiency caused by compound heterozygosity for two novel mutations in the prothrombin gene associated with a bleeding tendency.
    Stanchev H; Philips M; Villoutreix BO; Aksglaede L; Lethagen S; Thorsen S
    Thromb Haemost; 2006 Jan; 95(1):195-8. PubMed ID: 16543981
    [No Abstract]   [Full Text] [Related]  

  • 25. Prothrombin Molise I: documentation of a second incidence of replacement of a critical Arg near the active site.
    James HL; Kim DJ; Zheng DQ; Girolami A
    Thromb Res; 1995 Nov; 80(4):363-6. PubMed ID: 8585050
    [No Abstract]   [Full Text] [Related]  

  • 26. [Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations].
    Zhou RF; Fu QH; Xu XC; Wang WB; Wu WM; Ding QL; Xie S; Zhai ZM; Hu YQ; Wang XF; Wu JS; Wang HL
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):129-32. PubMed ID: 15946520
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Double mutation, a 2-bp deletion and Val211Ile, in the blood coagulation factor IX gene of a patient with severe hemophilia B].
    Seita I; Shinozawa K; Otaki M; Fujita S; Suzuki T; Amano K; Inaba H; Fukutake K
    Rinsho Byori; 2009 May; 57(5):417-24. PubMed ID: 19522246
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Factor VII Mie: homozygous asymptomatic type I deficiency caused by an amino acid substitution of His (CAC) for Arg(247) (CGC) in the catalytic domain.
    Ohiwa M; Hayashi T; Wada H; Minamikawa K; Shirakawa S; Suzuki K
    Thromb Haemost; 1994 Jun; 71(6):773-7. PubMed ID: 7974346
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Congenital prothrombin deficiency.
    Lancellotti S; De Cristofaro R
    Semin Thromb Hemost; 2009 Jun; 35(4):367-81. PubMed ID: 19598065
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prothrombin carora: hypoprothrombinaemia caused by substitution of Tyr-44 by Cys.
    Sun WY; Ruiz-Saez A; Burkart MC; Bosch N; Degen SJ
    Br J Haematol; 1999 Jun; 105(3):670-2. PubMed ID: 10354129
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. A new variant of human prothrombin: prothrombin Metz, demonstration in a family showing double heterozygosity for congenital hypoprothrombinemia and dysprothrombinemia.
    Josso F; Rio Y; Béguin S
    Haemostasis; 1982; 12(4):309-16. PubMed ID: 7152370
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A compound heterozygote for a novel missense mutation (G105R) in exon 3 and a missense mutation (D204E) in exon 5 of the lipoprotein lipase gene in a Japanese infant with hyperchylomicronaemia.
    Ikeda Y; Goji K; Takagi A
    Clin Sci (Lond); 2000 Dec; 99(6):569-78. PubMed ID: 11099402
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prothrombin Himi: a compound heterozygote for two dysfunctional prothrombin molecules (Met-337-->Thr and Arg-388-->His).
    Morishita E; Saito M; Kumabashiri I; Asakura H; Matsuda T; Yamaguchi K
    Blood; 1992 Nov; 80(9):2275-80. PubMed ID: 1421398
    [TBL] [Abstract][Full Text] [Related]  

  • 35. True congenital prothrombin deficiency due to a 'new' mutation in the pre-propeptide (ARG-39 GLN).
    Girolami A; Santarossa L; Scarparo P; Candeo N; Girolami B
    Acta Haematol; 2008; 120(2):82-6. PubMed ID: 18852482
    [No Abstract]   [Full Text] [Related]  

  • 36. [Analysis of mutation in heavy chain-micro (microHC) gene in a Chinese patient with congenital agammaglobulinemia].
    Zhang ZY; Zhao XD; Wang M; Zhang Y; Zhao Y; Yang XQ
    Zhonghua Er Ke Za Zhi; 2010 Apr; 48(4):279-83. PubMed ID: 20654017
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Simultaneous detection of FV Q506 and prothrombin 20210 A variation by allele-specific PCR.
    Mitterer M; Lanthaler AJ; Mair W; Giacomuzzi K; Coser P
    Haematologica; 1999 Mar; 84(3):204-7. PubMed ID: 10189382
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Molecular analysis of two pedigrees with inherited coagulation factor VII deficiency].
    Liang WL; Wei HY; Lin FQ; Zhou JL
    Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):817-20. PubMed ID: 23302610
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prothrombin Suresnes: a case of homozygous F299V mutation responsible for hypodysprothrombinemia.
    François D; Chevreaud C; Vignon D; de Mazancourt P
    Haematologica; 2006 Mar; 91(3):431-2. PubMed ID: 16503555
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Molecular genetic analysis for a pedigree with severe hereditary coagulation factor VII deficiency].
    Ding QL; Wang HL; Wang XF; Wang MS; Fu QH; Wu WM; Hu YQ; Wang ZY
    Zhonghua Nei Ke Za Zhi; 2003 Oct; 42(10):692-6. PubMed ID: 14633462
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.