91 related articles for article (PubMed ID: 8398833)
1. A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiency.
Wacey AI; Pemberton S; Cooper DN; Kakkar VV; Tuddenham EG
Br J Haematol; 1993 Jun; 84(2):290-300. PubMed ID: 8398833
[TBL] [Abstract][Full Text] [Related]
2. Structural basis for type I and type II deficiencies of antithrombotic plasma protein C: patterns revealed by three-dimensional molecular modelling of mutations of the protease domain.
Greengard JS; Fisher CL; Villoutreix B; Griffin JH
Proteins; 1994 Apr; 18(4):367-80. PubMed ID: 8208728
[TBL] [Abstract][Full Text] [Related]
3. A molecular model of a point mutation (Val297Met) in the serine protease domain of protein C.
Song KS; Park YS; Choi JR; Kim HK; Park Q
Exp Mol Med; 1999 Mar; 31(1):47-51. PubMed ID: 10231023
[TBL] [Abstract][Full Text] [Related]
4. A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic disease.
Millar DS; Wacey AI; Voke J; Kakkar VV; Cooper DN
Blood Coagul Fibrinolysis; 1993 Aug; 4(4):631-3. PubMed ID: 8218861
[TBL] [Abstract][Full Text] [Related]
5. Models of the serine protease domain of the human antithrombotic plasma factor activated protein C and its zymogen.
Fisher CL; Greengard JS; Griffin JH
Protein Sci; 1994 Apr; 3(4):588-99. PubMed ID: 8003977
[TBL] [Abstract][Full Text] [Related]
6. Possible structural implications of 20 mutations in the protein C protease domain.
Greengard JS; Griffin JH; Fisher CL
Thromb Haemost; 1994 Dec; 72(6):869-73. PubMed ID: 7740456
[TBL] [Abstract][Full Text] [Related]
7. CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining tool.
Saunders RE; Perkins SJ
Hum Mutat; 2008 Mar; 29(3):333-44. PubMed ID: 18058827
[TBL] [Abstract][Full Text] [Related]
8. Characterization of a thrombomodulin binding site on protein C and its comparison to an activated protein C binding site for factor Va.
Gale AJ; Griffin JH
Proteins; 2004 Feb; 54(3):433-41. PubMed ID: 14747992
[TBL] [Abstract][Full Text] [Related]
9. Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocket.
Marchetti G; Patracchini P; Gemmati D; Castaman G; Rodeghiero F; Wacey A; Cooper DN; Tuddenham EG; Bernardi F
Br J Haematol; 1993 Jun; 84(2):285-9. PubMed ID: 8398832
[TBL] [Abstract][Full Text] [Related]
10. Mapping active sites of blood coagulation serine proteases--activated protein C and thrombin--on simple graphics models.
Toma K; Suzuki K
J Mol Graph; 1989 Sep; 7(3):146-9, 154-5. PubMed ID: 2488854
[TBL] [Abstract][Full Text] [Related]
11. Amino acids 225-235** of the protein C serine-protease domain are important for the interaction with the thrombin-thrombomodulin complex.
Vincenot A; Gaussem P; Pittet JL; Debost S; Aiach M
FEBS Lett; 1995 Jun; 367(2):153-7. PubMed ID: 7540990
[TBL] [Abstract][Full Text] [Related]
12. A novel missense mutation (Thr176-->Ile) at the putative hinge of the neo N-terminus of activated protein C.
Hallam PJ; Wacey AI; Mannucci PM; Legnani C; Kühnau W; Krawczak M; Kakkar VV; Cooper DN
Hum Genet; 1995 Apr; 95(4):447-50. PubMed ID: 7705844
[TBL] [Abstract][Full Text] [Related]
13. Direct expression of recombinant activated human protein C, a serine protease.
Ehrlich HJ; Jaskunas SR; Grinnell BW; Yan SB; Bang NU
J Biol Chem; 1989 Aug; 264(24):14298-304. PubMed ID: 2668284
[TBL] [Abstract][Full Text] [Related]
14. Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency.
Peyvandi F; Jenkins PV; Mannucci PM; Billio A; Zeinali S; Perkins SJ; Perry DJ
Thromb Haemost; 2000 Aug; 84(2):250-7. PubMed ID: 10959697
[TBL] [Abstract][Full Text] [Related]
15. Cellular basis for protein C deficiency caused by a single amino acid substitution at Arg15 in the gamma-carboxyglutamic acid domain.
Tokunaga F; Tsukamoto T; Koide T
J Biochem; 1996 Aug; 120(2):360-8. PubMed ID: 8889822
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. [Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency].
Yang L; Jin Y; Yang T; Chen X; Zhu L; Wang M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):10-14. PubMed ID: 28186585
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
