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 *

117 related articles for article (PubMed ID: 17522339)

  • 21. Novel frameshift mutation (Pro171fsX21) in neonatal type 2 Gaucher's disease.
    Park HW; Lee Y; Kim GH; Lee BS; Kim KS; Yoo HW; Kim EA
    Gene; 2012 Oct; 507(2):170-3. PubMed ID: 22772462
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Antithrombotic potential of the contact activation pathway.
    Schmaier AH
    Curr Opin Hematol; 2016 Sep; 23(5):445-52. PubMed ID: 27380557
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency.
    Yang LH; Zheng FX; Chen Y; Jin YH; Zhang Z; Xie HX; Yang XL; Wang MS; Chen BC
    Blood Coagul Fibrinolysis; 2014 Dec; 25(8):824-30. PubMed ID: 24911457
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Type I antithrombin deficiency due to 13389G deletion in antithrombin gene].
    Fu Q; Xu X; Ding Q; Hu Y; Wang X; Wang H
    Zhonghua Xue Ye Xue Za Zhi; 2002 Nov; 23(11):588-90. PubMed ID: 12482344
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [A case of high molecular weight kininogen deficiency--problem of its laboratory diagnosis and low molecular weight kininogen].
    Komiyama Y; Nishikado H; Egawa H; Murata K; Munakata M; Teraoka A; Okubo S; Yasunaga K
    Nihon Ketsueki Gakkai Zasshi; 1987 Aug; 50(5):1047-53. PubMed ID: 3324605
    [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. [Laboratory values of kallikrein-kininogen-kinin].
    Omata K
    Nihon Rinsho; 2005 Aug; 63 Suppl 8():573-6. PubMed ID: 16149580
    [No Abstract]   [Full Text] [Related]  

  • 28. Primary structures of guinea pig high- and low-molecular-weight kininogens.
    Semba U; Umeda Y; Shibuya Y; Okabe H; Tanase S; Yamamoto T
    Int Immunopharmacol; 2004 Oct; 4(10-11):1391-400. PubMed ID: 15313436
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Five antithrombin variants, four associated with thrombosis.
    Fitton HL; Walker ID; Jones L; Brown K; Carrell RW; Coughlin P
    Blood Coagul Fibrinolysis; 1997 Mar; 8(2):145-8. PubMed ID: 9518046
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Tachibana trait: human high molecular weight kininogen deficiency with diminished levels of prekallikrein and low molecular weight kininogen.
    Nakamura K; Iijima K; Fukuda C; Kadowaki H; Ikoma H; Oh-ishi S; Uchida Y; Katori M
    Nihon Ketsueki Gakkai Zasshi; 1985 Sep; 48(6):1473-9. PubMed ID: 3853954
    [No Abstract]   [Full Text] [Related]  

  • 31. Molecular characterization of total kininogen deficiency in Japanese patients.
    Ishimaru F; Dansako H; Nakase K; Fujii N; Sezaki N; Nakayama H; Fujii N; Komiyama Y; Iijima K; Takenaka K; Teshima T; Shinagawa K; Ikeda K; Niiya K; Harada M
    Int J Hematol; 1999 Feb; 69(2):126-8. PubMed ID: 10071463
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Severe coagulation factor V deficiency caused by a 4 bp deletion in the factor V gene.
    Guasch JF; Cannegieter S; Reitsma PH; van't Veer-Korthof ET; Bertina RM
    Br J Haematol; 1998 Apr; 101(1):32-9. PubMed ID: 9576178
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The first cases of Fitzgerald factor deficiency in the Orient: three cases in one family.
    Hayashi H; Koya H; Kuroda M; Kitazima K; Kimura I; Katori M; Oh-ishi S
    Acta Haematol; 1980; 63(2):107-13. PubMed ID: 6768213
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Six additional mutations in fucosidosis: three nonsense mutations and three frameshift mutations.
    Seo HC; Willems PJ; O'Brien JS
    Hum Mol Genet; 1993 Aug; 2(8):1205-8. PubMed ID: 8401503
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Partial rescue of human carbonic anhydrase II frameshift mutation by ribosomal frameshift.
    Hu PY; Waheed A; Sly WS
    Proc Natl Acad Sci U S A; 1995 Mar; 92(6):2136-40. PubMed ID: 7892236
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyria.
    Todd DJ; Hughes AE; Ennis KT; Ward AJ; Burrows D; Nevin NC
    Hum Mol Genet; 1993 Sep; 2(9):1495-6. PubMed ID: 8242081
    [No Abstract]   [Full Text] [Related]  

  • 38. Novel deleterious mutation in the F12 gene in a Korean family with severe coagulation factor XII deficiency.
    Kim HJ; Kim HJ; Kwon EH; Lee KO; Park IA; Kim SH
    Blood Coagul Fibrinolysis; 2010 Oct; 21(7):683-6. PubMed ID: 20729721
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [High molecular weight kininogen in inflammation and angiogenesis: a review of its properties and therapeutic applications].
    Isordia-Salas I; Sainz IM; Pixley RA; Martínez-Murillo C; Colman RW
    Rev Invest Clin; 2005; 57(6):802-13. PubMed ID: 16708906
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Characterization of the murine gene of gC1qBP, a novel cell protein that binds the globular heads of C1q, vitronectin, high molecular weight kininogen and factor XII.
    Lim BL; White RA; Hummel GS; Schwaeble W; Lynch NJ; Peerschke EI; Reid KB; Ghebrehiwet B
    Gene; 1998 Mar; 209(1-2):229-37. PubMed ID: 9524273
    [TBL] [Abstract][Full Text] [Related]  

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