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Journal Abstract Search

180 related items for PubMed ID: 10828024

  • 1. Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies.
    Pinotti M, Toso R, Girelli D, Bindini D, Ferraresi P, Papa ML, Corrocher R, Marchetti G, Bernardi F.
    Blood; 2000 Jun 01; 95(11):3423-8. PubMed ID: 10828024
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  • 2. Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma.
    Bernardi F, Marchetti G, Pinotti M, Arcieri P, Baroncini C, Papacchini M, Zepponi E, Ursicino N, Chiarotti F, Mariani G.
    Arterioscler Thromb Vasc Biol; 1996 Jan 01; 16(1):72-6. PubMed ID: 8548429
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  • 3. F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study.
    Quintavalle G, Riccardi F, Rivolta GF, Martorana D, Di Perna C, Percesepe A, Tagliaferri A, Ad-Hoc Study Group.
    Thromb Haemost; 2017 Aug 01; 117(8):1455-1464. PubMed ID: 28447100
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  • 4. Contribution of factor VII genotype to activated FVII levels. Differences in genotype frequencies between northern and southern European populations.
    Bernardi F, Arcieri P, Bertina RM, Chiarotti F, Corral J, Pinotti M, Prydz H, Samama M, Sandset PM, Strom R, Garcia VV, Mariani G.
    Arterioscler Thromb Vasc Biol; 1997 Nov 01; 17(11):2548-53. PubMed ID: 9409226
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  • 5. Polymorphisms of the coagulation factor VII gene and its plasma levels in relation to acute cerebral infarction differences in allelic frequencies between Chinese Han and European populations.
    Kang WY, Wang HL, Xiong LF, Wang XF, Chu HY, Qu B, Liu XF, Yin J, Duan BH, Wang ZY.
    Chin Med J (Engl); 2004 Jan 01; 117(1):71-4. PubMed ID: 14733777
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  • 6. Genotype associations of factor VII gene with plasma factor VII coagulant activity and antigen levels in healthy Chinese.
    Liu Y, Heng CK, Saha N, Hong S, Low PS.
    Blood Coagul Fibrinolysis; 2002 Apr 01; 13(3):217-24. PubMed ID: 11943935
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  • 7. Complexity of the genetic contribution to factor VII deficiency in two Spanish families: clinical and biological implications.
    Sabater-Lleal M, Martínez-Marchán E, Martínez-Sánchez E, Coll M, Vallvé C, Mateo J, Souto JC, Fontcuberta J, Soria JM.
    Haematologica; 2003 Aug 01; 88(8):906-13. PubMed ID: 12935978
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  • 8. Molecular analysis of the genotype-phenotype relationship in factor VII deficiency.
    Millar DS, Kemball-Cook G, McVey JH, Tuddenham EG, Mumford AD, Attock GB, Reverter JC, Lanir N, Parapia LA, Reynaud J, Meili E, von Felton A, Martinowitz U, Prangnell DR, Krawczak M, Cooper DN.
    Hum Genet; 2000 Oct 01; 107(4):327-42. PubMed ID: 11129332
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  • 10. A novel missense mutation close to the charge-stabilizing system in a patient with congenital factor VII deficiency.
    Jiang M, Wang Z, Yu Z, Bai X, Su J, Cao L, Zhang W, Ruan C.
    Blood Coagul Fibrinolysis; 2011 Jun 01; 22(4):264-70. PubMed ID: 21372693
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  • 12. Two common functional polymorphisms in the promoter region of the coagulation factor VII gene determining plasma factor VII activity and mass concentration.
    van 't Hooft FM, Silveira A, Tornvall P, Iliadou A, Ehrenborg E, Eriksson P, Hamsten A.
    Blood; 1999 May 15; 93(10):3432-41. PubMed ID: 10233895
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  • 13. Activated FVII levels in factor VII Padua (Arg304Gln) coagulation disorder and in true factor VII deficiency: a study in homozygotes and heterozygotes.
    Girolami A, Bertozzi I, de Marinis GB, Bonamigo E, Fabris F.
    Hematology; 2011 Sep 15; 16(5):308-12. PubMed ID: 21902896
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  • 14. Coagulation factor VII, R353Q polymorphism, and serum choline-containing phospholipids in males at high risk for coronary heart disease.
    Lindman AS, Pedersen JI, Arnesen H, Hjerkinn EM, Veierød MB, Prydz H, Seljeflot I.
    Thromb Res; 2004 Sep 15; 113(1):57-65. PubMed ID: 15081566
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