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 *

110 related articles for article (PubMed ID: 9414311)

  • 21. New molecular insights into the genetics of thrombophilia. Resistance to activated protein C caused by Arg506 to Gln mutation in factor V as a pathogenic risk factor for venous thrombosis.
    Dahlbäck B
    Thromb Haemost; 1995 Jul; 74(1):139-48. PubMed ID: 8578447
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The p49/TaqI Y-specific polymorphisms in three groups of Indians.
    Lucotte G; Sriniva KR; Loirat F; Hazout S; Ruffié J
    Gene Geogr; 1990 Apr; 4(1):21-7. PubMed ID: 1980603
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Discrimination between normal wildtype and carriers of coagulation factor V Leiden mutation by the activated protein C resistance test in the presence of factor V deficient plasma.
    Reuner KH; Litfin F; Patscheke H
    Eur J Clin Chem Clin Biochem; 1997 Jan; 35(1):41-5. PubMed ID: 9156566
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Factor V deficiency caused by a novel missense mutation, Ile417Thr, in the A2 domain.
    Kling SJ; Griffee M; Flanders MM; Rodgers GM
    J Thromb Haemost; 2006 Feb; 4(2):481-3. PubMed ID: 16420587
    [No Abstract]   [Full Text] [Related]  

  • 25. Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leiden.
    Beauchamp NJ; Daly ME; Cooper PC; Makris M; Preston FE; Peake IR
    Blood; 1996 Sep; 88(5):1700-7. PubMed ID: 8781426
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency.
    Bafunno V; Favuzzi G; Fierro T; Chetta M; Mastrodicasa E; Chinni E; Grandone E; Margaglione M; Gresele P
    Haemophilia; 2012 Mar; 18(2):e51-3. PubMed ID: 22251029
    [No Abstract]   [Full Text] [Related]  

  • 27. A PstI polymorphism in the human coagulation factor V (F5) gene.
    McAlpine PJ; Dixon M; Guinto ER; MacGillivray RT
    Nucleic Acids Res; 1990 Dec; 18(24):7471. PubMed ID: 1979680
    [No Abstract]   [Full Text] [Related]  

  • 28. A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population.
    Castoldi E; Lunghi B; Mingozzi F; Muleo G; Redaelli R; Mariani G; Bernardi F
    Haematologica; 2001 Jun; 86(6):629-33. PubMed ID: 11418372
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Joint effect of G1691A factor V point mutation and factor VII Arg/Gln(353) gene polymorphism on the risk of premature coronary artery disease.
    Petrovic D; Zorc M; Keber I; Peterlin B
    Ann Genet; 2001; 44(1):33-6. PubMed ID: 11334615
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Factor V New Brunswick: Ala221Val associated with FV deficiency reproduced in vitro and functionally characterized.
    Steen M; Miteva M; Villoutreix BO; Yamazaki T; Dahlbäck B
    Blood; 2003 Aug; 102(4):1316-22. PubMed ID: 12714495
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular characterization of a type I quantitative factor V deficiency in a thrombosis patient that is "pseudo homozygous" for activated protein C resistance.
    Guasch JF; Lensen RP; Bertina RM
    Thromb Haemost; 1997 Feb; 77(2):252-7. PubMed ID: 9157576
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Identification of two novel mutations of human blood coagulation factor V gene in a Chinese family with congenital factor V deficiency].
    Zheng WD; Liu YH; Liu HF; Chen ZH; Wang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Oct; 23(5):515-8. PubMed ID: 17029198
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Factor V Arg2074Cys: a novel missense mutation in the C2 domain of factor V.
    Bossone A; D'Angelo F; Santacroce R; De Lucia D; Margaglione M
    Thromb Haemost; 2002 May; 87(5):923-4. PubMed ID: 12038802
    [No Abstract]   [Full Text] [Related]  

  • 34. Arylsulfatase A pseudodeficiency: a common polymorphism which is associated with a unique haplotype.
    Zlotogora J; Furman-Shaharabani Y; Goldenfum S; Winchester B; von Figura K; Gieselmann V
    Am J Med Genet; 1994 Aug; 52(2):146-50. PubMed ID: 7801999
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Factor V Kuwait alias factor V R3: a rare polymorphism of uncertain functional significance.
    Castoldi E; Lunghi B; Rosing J; Bernardi F
    Med Princ Pract; 2007; 16(3):244-5; author reply 246. PubMed ID: 17409764
    [No Abstract]   [Full Text] [Related]  

  • 36. Pseudo-homozygous activated protein C resistance due to coinheritance of heterozygous factor V Leiden mutation and type I factor V deficiency. Variable expression when analyzed by different activated protein C resistance functional assays.
    Delahousse B; Iochmann S; Pouplard C; Fimbel B; Charbonnier B; Gruel Y
    Blood Coagul Fibrinolysis; 1997 Nov; 8(8):503-9. PubMed ID: 9491268
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain.
    Asselta R; Montefusco MC; Duga S; Malcovati M; Peyvandi F; Mannucci PM; Tenchini ML
    J Thromb Haemost; 2003 Jun; 1(6):1237-44. PubMed ID: 12871325
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: a study of 150 families.
    Martinelli I; Mannucci PM; De Stefano V; Taioli E; Rossi V; Crosti F; Paciaroni K; Leone G; Faioni EM
    Blood; 1998 Oct; 92(7):2353-8. PubMed ID: 9746774
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Portal vein thrombosis and factor V Arg 506 to Gln mutation.
    Levoir D; Emmerich J; Alhenc-Gelas M; Dumontier I; Petite JP; Fiessinger JN; Aiach M
    Thromb Haemost; 1995 Mar; 73(3):550-1. PubMed ID: 7667842
    [No Abstract]   [Full Text] [Related]  

  • 40. Resistance to activated protein C due to mutated factor V as a novel cause of inherited thrombophilia.
    De Stefano V; Leone G
    Haematologica; 1995; 80(4):344-56. PubMed ID: 7590506
    [TBL] [Abstract][Full Text] [Related]  

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