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 *

126 related articles for article (PubMed ID: 7795152)

  • 1. Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His.
    Alhenc-Gelas M; Emmerich J; Gandrille S; Aubry ML; Benaily N; Fiessinger JN; Aiach M
    Blood Coagul Fibrinolysis; 1995 Feb; 6(1):35-41. PubMed ID: 7795152
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosis.
    Grundy CB; Schulman S; Tengborn L; Kakkar VV; Cooper DN
    Hum Genet; 1992 Aug; 89(6):685-6. PubMed ID: 1511989
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Replacement therapy with a purified protein C concentrate during initiation of oral anticoagulation in severe protein C congenital deficiency.
    De Stefano V; Mastrangelo S; Schwarz HP; Pola P; Flore R; Bizzi B; Leone G
    Thromb Haemost; 1993 Aug; 70(2):247-9. PubMed ID: 8236128
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Protein C deficiency resulting from possible double heterozygosity and its response to danazol.
    Gruppo RA; Leimer P; Francis RB; Marlar RA; Silberstein E
    Blood; 1988 Feb; 71(2):370-4. PubMed ID: 3337902
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel (R(-11)C; T394D) and two repeat missense mutations in the protein C gene associated with venous thrombosis in six kindreds.
    Ireland HA; Boisclair MD; Taylor J; Thompson E; Thein SL; Girolami A; De Caterina M; Scopacasa F; De Stefano V; Leone G; Finazzi G; Cohen H; Lane DA
    Hum Mutat; 1996; 7(2):176-9. PubMed ID: 8829639
    [No Abstract]   [Full Text] [Related]  

  • 6. [A pedigree analysis of pulmonary embolism caused by compound heterozygous mutations of protein C].
    Ye X; Liu X; Feng Y; Ding Q; Zhou X; Wang X
    Nan Fang Yi Ke Da Xue Xue Bao; 2012 Jan; 32(1):109-12. PubMed ID: 22366017
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Compound heterozygous protein C deficiency caused by two mutations, Arg-178 to Gln and Cys-331 to Arg, leading to impaired secretion of mutant protein C.
    Sugahara Y; Miura O; Hirosawa S; Aoki N
    Thromb Haemost; 1994 Dec; 72(6):814-8. PubMed ID: 7740447
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Six missense mutations associated with type I and type II protein C deficiency and implications obtained from molecular modelling.
    Zheng YZ; Sakata T; Matsusue T; Umeyama H; Kato H; Miyata T
    Blood Coagul Fibrinolysis; 1994 Oct; 5(5):687-96. PubMed ID: 7865674
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Gene diagnosis of four patients with protein C deficiency].
    Gao B; Zhou RF; Ouyang J; Chen B; Xu Y; Li P
    Zhonghua Xue Ye Xue Za Zhi; 2016 Nov; 37(11):966-970. PubMed ID: 27995882
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Successful protein C concentrate administration during initiation of oral anticoagulation in adult patients with severe congenital protein C deficiency: report of two cases.
    Imberti D; Pierfranceschi MG
    Pathophysiol Haemost Thromb; 2008; 36(2):53-7. PubMed ID: 19127082
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel dysfunctional protein C (protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg-1 results in a strongly reduced affinity for binding of Ca++.
    Girolami A; Simioni P; Girolami B; Marchiori A; Millar DS; Bignell P; Kakkar VV; Cooper DN
    Br J Haematol; 1993 Nov; 85(3):521-7. PubMed ID: 8136274
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Homozygosity for R87H missense mutation and for a rare intron 7 DNA variant (7054G --> A) in the PROC genes of three siblings initially classified as heterozygotes for protein C deficiency.
    Soria JM; Morell M; Nicolau I; Estivill X; Sala N
    Blood Coagul Fibrinolysis; 1996 Jan; 7(1):15-23. PubMed ID: 8845458
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Different impact of two mutations of a novel compound heterozygous protein C deficiency with late onset thrombosis.
    Yang LH; Wang MS; Zheng FX; Li J; Chen Y; Jin YH; Xie HX; Yang XL; Chen BC
    Genet Mol Res; 2014 Apr; 13(2):2969-77. PubMed ID: 24782131
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Severe congenital protein C deficiency: description of a new mutation and prophylactic protein C therapy and in vivo pharmacokinetics.
    Tcheng WY; Dovat S; Gurel Z; Donkin J; Wong WY
    J Pediatr Hematol Oncol; 2008 Feb; 30(2):166-71. PubMed ID: 18376272
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. Recurrent superficial venous thrombophlebitis because of mutations in the protein C and fibrinogen genes in a young Argentinian female.
    Guglielmone HA; Bastos L; Jarchum GD; Alvarez-Bollea MA
    Blood Coagul Fibrinolysis; 2019 Mar; 30(2):80-84. PubMed ID: 30632992
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Five novel mutations located in exons III and IX of the protein C gene in patients presenting with defective protein C anticoagulant activity.
    Gandrille S; Alhenc-Gelas M; Gaussem P; Aillaud MF; Dupuy E; Juhan-Vague I; Aiach M
    Blood; 1993 Jul; 82(1):159-68. PubMed ID: 8324221
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.