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 *

243 related articles for article (PubMed ID: 11686318)

  • 1. Abnormal propeptide processing resulting in the presence of two abnormal species of protein C in plasma: characterization of the dysfunctional protein C Padua3 (protein C(R-1L/propeptide)).
    Simioni P; Kalafatis M; Tormene D; Luni S; Zerbinati P; Barzon L; Palù G; Girolami A
    Thromb Haemost; 2001 Oct; 86(4):1017-22. PubMed ID: 11686318
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Protein C Osaka 10 with aberrant propeptide processing: loss of anticoagulant activity due to an amino acid substitution in the protein C precursor.
    Miyata T; Zheng YZ; Sakata T; Kato H
    Thromb Haemost; 1995 Oct; 74(4):1003-8. PubMed ID: 8560401
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The protein C omega-loop substitution Asn2Ile is associated with reduced protein C anticoagulant activity.
    Preston RJ; Morse C; Murden SL; Brady SK; O'Donnell JS; Mumford AD
    Br J Haematol; 2009 Mar; 144(6):946-53. PubMed ID: 19133979
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Properties of a recombinant chimeric protein in which the gamma-carboxyglutamic acid and helical stack domains of human anticoagulant protein C are replaced by those of human coagulation factor VII.
    Geng JP; Castellino FJ
    Thromb Haemost; 1997 May; 77(5):926-33. PubMed ID: 9184404
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. Functional consequences of mutations in amino acid residues that stabilize calcium binding to the first epidermal growth factor homology domain of human protein C.
    Geng JP; Cheng CH; Castellino FJ
    Thromb Haemost; 1996 Nov; 76(5):720-8. PubMed ID: 8950780
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Defective sorting to secretory vesicles in trans-Golgi network is partly responsible for protein C deficiency: molecular mechanisms of impaired secretion of abnormal protein C R169W, R352W, and G376D.
    Naito M; Mimuro J; Endo H; Madoiwa S; Ogata K; Kikuchi J; Sugo T; Yasu T; Kariya Y; Hoshino Y; Sakata Y
    Circ Res; 2003 May; 92(8):865-72. PubMed ID: 12663483
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The hydrophobic nature of residue-5 of human protein C is a major determinant of its functional interactions with acidic phospholipid vesicles.
    Jalbert LR; Chan JC; Christiansen WT; Castellino FJ
    Biochemistry; 1996 Jun; 35(22):7093-9. PubMed ID: 8679535
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency.
    Miyata T; Zheng YZ; Sakata T; Tsushima N; Kato H
    Thromb Haemost; 1994 Jan; 71(1):32-7. PubMed ID: 8165644
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An abnormal protein C (protein C Yonago) with an amino acid substitution of Gly for Arg-15 caused by a single base mutation of C to G in codon 57 (CGG-->GGG). Deteriorated calcium-dependent conformation of the gamma-carboxyglutamic acid domain relevant to a thrombotic tendency.
    Mimuro J; Muramatsu S; Kaneko M; Yoshitake S; Iijima K; Nakamura K; Sakata Y; Matsuda M
    Int J Hematol; 1993 Jan; 57(1):9-14. PubMed ID: 8477066
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Protein C Sapporo (protein C Glu 25 --> Lys): a heterozygous missense mutation in the Gla domain provides new insight into the interaction between protein C and endothelial protein C receptor.
    Nakabayashi T; Mizukami K; Naitoh S; Takeda M; Shikamoto Y; Nakagawa T; Kaneko H; Tarumi T; Mizoguchi I; Mizuno H; Ieko M; Koike T
    Thromb Haemost; 2005 Nov; 94(5):942-50. PubMed ID: 16363234
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].
    Zhou RF; Wang HL; Fu QH; Wang WB; Wu WM; Ding QL; Xie S; Hu YQ; Wang XF; Wang ZY
    Zhonghua Yi Xue Za Zhi; 2003 Oct; 83(19):1694-7. PubMed ID: 14642106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Naturally occurring Arg(-1) to His mutation in human protein C leads to aberrant propeptide processing and secretion of dysfunctional protein C.
    Lind B; Johnsen AH; Thorsen S
    Blood; 1997 Apr; 89(8):2807-16. PubMed ID: 9108399
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.
    Tjeldhorn L; Sandset PM; Haugbro K; Skretting G
    Thromb Res; 2010 Mar; 125(3):230-4. PubMed ID: 19535131
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Protein C deficiency: identification of a novel two-base pair insertion and two point mutations in exon 7 of the protein C gene in Spanish families.
    Soria JM; Fontcuberta J; Borrell M; Estivill X; Sala N
    Hum Mutat; 1992; 1(5):428-31. PubMed ID: 1301954
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A compound heterozygous protein C deficiency with a single nucleotide G deletion encoding Gly-381 and an amino acid substitution of Lys for Gla-26.
    Ido M; Ohiwa M; Hayashi T; Nishioka J; Hatada T; Watanabe Y; Wada H; Shirakawa S; Suzuki K
    Thromb Haemost; 1993 Oct; 70(4):636-41. PubMed ID: 8115990
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [A point mutation at Arg169 (CGG-->TGG) in hereditary protein C deficiency].
    Morishita E; Asakura H; Saito M; Yamazaki M; Ontachi Y; Mizutani T; Kato M; Nakao S
    Rinsho Ketsueki; 2001 Feb; 42(2):104-9. PubMed ID: 11280915
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis.
    Gandrille S; Vidaud M; Aiach M; Alhenc-Gelas M; Fischer AM; Gouault-Heilman M; Toulon P; Fiessinger JN; Goossens M
    Hum Mutat; 1992; 1(6):491-500. PubMed ID: 1301959
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Six different point mutations in seven Danish families with symptomatic protein C deficiency.
    Lind B; Schwartz M; Thorsen S
    Thromb Haemost; 1995 Feb; 73(2):186-93. PubMed ID: 7792728
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.