146 related articles for article (PubMed ID: 7482420)
1. Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH.
Reitsma PH; Bernardi F; Doig RG; Gandrille S; Greengard JS; Ireland H; Krawczak M; Lind B; Long GL; Poort SR
Thromb Haemost; 1995 May; 73(5):876-89. PubMed ID: 7482420
[No Abstract] [Full Text] [Related]
2. Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Reitsma PH; Poort SR; Bernardi F; Gandrille S; Long GL; Sala N; Cooper DN
Thromb Haemost; 1993 Jan; 69(1):77-84. PubMed ID: 8446940
[No Abstract] [Full Text] [Related]
3. Analysis of mutations occurring at the human hprt locus.
Cariello NF; Skopek TR
J Mol Biol; 1993 May; 231(1):41-57. PubMed ID: 8496965
[TBL] [Abstract][Full Text] [Related]
4. Protein S deficiency: a database of mutations. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Gandrille S; Borgel D; Ireland H; Lane DA; Simmonds R; Reitsma PH; Mannhalter C; Pabinger I; Saito H; Suzuki K; Formstone C; Cooper DN; Espinosa Y; Sala N; Bernardi F; Aiach M
Thromb Haemost; 1997 Jun; 77(6):1201-14. PubMed ID: 9241758
[No Abstract] [Full Text] [Related]
5. A review of mutations causing deficiencies of antithrombin, protein C and protein S.
Aiach M; Gandrille S; Emmerich J
Thromb Haemost; 1995 Jul; 74(1):81-9. PubMed ID: 8578531
[TBL] [Abstract][Full Text] [Related]
6. Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency.
Yamamoto K; Tanimoto M; Emi N; Matsushita T; Takamatsu J; Saito H
J Clin Invest; 1992 Dec; 90(6):2439-46. PubMed ID: 1469096
[TBL] [Abstract][Full Text] [Related]
7. Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Lane DA; Bayston T; Olds RJ; Fitches AC; Cooper DN; Millar DS; Jochmans K; Perry DJ; Okajima K; Thein SL; Emmerich J
Thromb Haemost; 1997 Jan; 77(1):197-211. PubMed ID: 9031473
[No Abstract] [Full Text] [Related]
8. Novel human pathological mutations. Gene symbol: PROC. Disease: Protein C deficiency.
Pathare A; Al Zadjali S; Shah W
Hum Genet; 2009 Aug; 126(2):336-7. PubMed ID: 19694010
[No Abstract] [Full Text] [Related]
9. 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]
10. Type I protein C deficiency in French Canadians: evidence of a founder effect and association of specific protein C gene mutations with plasma protein C levels.
Couture P; Demers C; Morissette J; Delage R; Jomphe M; Couture L; Simard J
Thromb Haemost; 1998 Oct; 80(4):551-6. PubMed ID: 9798967
[TBL] [Abstract][Full Text] [Related]
11. Protein C deficiency: summary of the 1995 database update.
Reitsma PH
Nucleic Acids Res; 1996 Jan; 24(1):157-9. PubMed ID: 8594568
[TBL] [Abstract][Full Text] [Related]
12. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.
Ireland H; Thompson E; Lane DA
Thromb Haemost; 1996 Dec; 76(6):867-73. PubMed ID: 8972002
[TBL] [Abstract][Full Text] [Related]
13. Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene.
Doig RG; Begley CG; McGrath KM
Thromb Haemost; 1994 Aug; 72(2):203-8. PubMed ID: 7831652
[TBL] [Abstract][Full Text] [Related]
14. Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC gene.
Soria JM; Berg LP; Fontcuberta J; Kakkar VV; Estivill X; Cooper DN; Sala N
Thromb Haemost; 1996 Jun; 75(6):870-6. PubMed ID: 8822578
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.
Lane DA; Olds RJ; Boisclair M; Chowdhury V; Thein SL; Cooper DN; Blajchman M; Perry D; Emmerich J; Aiach M
Thromb Haemost; 1993 Aug; 70(2):361-9. PubMed ID: 8236149
[No Abstract] [Full Text] [Related]
17. Genetic mutations in ten unrelated American patients with symptomatic type 1 protein C deficiency.
Tsay W; Greengard JS; Montgomery RR; McPherson RA; Fucci JC; Koerper MA; Coughlin J; Griffin JH
Blood Coagul Fibrinolysis; 1993 Oct; 4(5):791-6. PubMed ID: 8292730
[TBL] [Abstract][Full Text] [Related]
18. Severe type I protein C deficiency in a compound heterozygote for Y124C and Q132X mutations in exon 6 of the PROC gene.
Soria JM; Morell M; Jiménez-Astorga C; Estivill X; Sala N
Thromb Haemost; 1995 Nov; 74(5):1215-20. PubMed ID: 8607097
[TBL] [Abstract][Full Text] [Related]
19. [Genetic analysis of congenital protein C deficiency].
Yamamoto S; Matsushita T
Rinsho Ketsueki; 1992 Jun; 33(6):750-5. PubMed ID: 1433913
[No Abstract] [Full Text] [Related]
20. Identification of one novel and three other point mutations in the protein C gene of five unrelated brazilian patients with hereditary protein C deficiency.
Singh YS; Arruda VR; Ozello MC; Machado TF; Annichino-Bizzacchi MM
Haematologica; 2000 Aug; 85(8):891-3. PubMed ID: 10942953
[No Abstract] [Full Text] [Related]
[Next] [New Search]