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2. Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population. Santamaría A, Mateo J, Tirado I, Oliver A, Belvís R, Martí-Fábregas J, Felices R, Soria JM, Souto JC, Fontcuberta J. Stroke; 2004 Aug; 35(8):1795-9. PubMed ID: 15232129 [Abstract] [Full Text] [Related]
3. Rapid detection of the 46C --> T polymorphism in the factor XII gene, a novel genetic risk factor for thrombosis, by melting peak analysis using fluorescence hybridization probes. Tirado I, Fontcuberta J, Soria JM. Genet Test; 2003 Aug; 7(4):295-301. PubMed ID: 15000805 [Abstract] [Full Text] [Related]
4. Factor XII C46T gene polymorphism and the risk of cerebral venous thrombosis. Reuner KH, Jenetzky E, Aleu A, Litfin F, Mellado P, Kloss M, Jüttler E, Grau AJ, Rickmann H, Patscheke H, Lichy C. Neurology; 2008 Jan 08; 70(2):129-32. PubMed ID: 18180442 [Abstract] [Full Text] [Related]
5. Homozygosity of the T allele of the 46 C-->T polymorphism in the F12 gene is a risk factor for acute coronary artery disease in the Spanish population. Santamaría A, Martínez-Rubio A, Mateo J, Tirado I, Soria JM, Fontcuberta J. Haematologica; 2004 Jul 08; 89(7):878-9. PubMed ID: 15257949 [Abstract] [Full Text] [Related]
6. Association of FXII 5'UTR 46C>T polymorphism with FXII activity and risk of thrombotic disease. Rasighaemi P, Kazemi A, Ala F, Jazebi M, Razmkhah F. Turk J Haematol; 2010 Mar 05; 27(1):15-9. PubMed ID: 27265792 [Abstract] [Full Text] [Related]
7. The 46C-->T polymorphism in the factor XII gene (F12) and the risk of venous thrombosis. Bertina RM, Poort SR, Vos HL, Rosendaal FR. J Thromb Haemost; 2005 Mar 05; 3(3):597-9. PubMed ID: 15748262 [No Abstract] [Full Text] [Related]
8. Factor XII 46C --> T gene polymorphism in Chilean subjects with coronary artery disease and controls. Caamaño J, Jaramillo PC, Lanas C, Lanas F, Salazar LA. Med Princ Pract; 2009 Mar 05; 18(2):137-42. PubMed ID: 19204433 [Abstract] [Full Text] [Related]
12. Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels. Calafell F, Almasy L, Sabater-Lleal M, Buil A, Mordillo C, Ramírez-Soriano A, Sikora M, Souto JC, Blangero J, Fontcuberta J, Soria JM. Hum Mol Genet; 2010 Feb 01; 19(3):517-25. PubMed ID: 19933701 [Abstract] [Full Text] [Related]
13. FXII (46C-->T) polymorphism and in vivo generation of FXII activity--gene frequencies and relationship in patients with coronary artery disease. Kohler HP, Futers TS, Grant PJ. Thromb Haemost; 1999 May 01; 81(5):745-7. PubMed ID: 10365748 [Abstract] [Full Text] [Related]
14. A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease. Soria JM, Almasy L, Souto JC, Bacq D, Buil A, Faure A, Martínez-Marchán E, Mateo J, Borrell M, Stone W, Lathrop M, Fontcuberta J, Blangero J. Am J Hum Genet; 2002 Mar 01; 70(3):567-74. PubMed ID: 11805911 [Abstract] [Full Text] [Related]
15. Activated factor XII levels are dependent on factor XII 46C/T genotypes and factor XII zymogen levels, and are associated with vascular risk factors in patients and healthy subjects. Ishii K, Oguchi S, Murata M, Mitsuyoshi Y, Takeshita E, Ito D, Tanahashi N, Fukuuchi Y, Oosumi K, Matsumoto K, Kitajima M, Yamamoto M, Watanabe G, Ikeda Y, Watanabe K. Blood Coagul Fibrinolysis; 2000 Apr 01; 11(3):277-84. PubMed ID: 10870808 [Abstract] [Full Text] [Related]
16. Factor XII gene (F12) -4C/C polymorphism in combination with low protein S activity is associated with deep vein thrombosis. Kanaji T, Watanabe K, Hattori S, Urata M, Iida H, Kinoshita S, Kayamori Y, Kang D, Hamasaki N. Thromb Haemost; 2006 Dec 01; 96(6):854-5. PubMed ID: 17139385 [No Abstract] [Full Text] [Related]
17. Major and potential prothrombotic genotypes in patients with venous thrombosis and in healthy subjects from Slovenia. Bedencic M, Bozic M, Peternel P, Stegnar M. Pathophysiol Haemost Thromb; 2008 Dec 01; 36(2):58-63. PubMed ID: 19127083 [Abstract] [Full Text] [Related]
18. Hageman factor C46T promoter gene polymorphism in patients with hypercortisolism. Świątkowska-Stodulska R, Kitowska A, Skibowska-Bielińska A, Wiśniewski P, Sworczak K. Horm Metab Res; 2014 Jun 01; 46(7):510-4. PubMed ID: 24691729 [Abstract] [Full Text] [Related]
19. Rebuttal: factor XII levels, factor XII 46 C>T polymorphism and venous thrombosis: a word of caution is needed. Girolami A, Sartori MT, Lombardi AM, Pellati D. Thromb Haemost; 2004 Oct 01; 92(4):892-3; author reply 894-5. PubMed ID: 15467923 [No Abstract] [Full Text] [Related]