Citations for
Factor VII and protein C are phosphatidic acid-binding proteins.
Tavoosi N, Smith SA, Davis-Harrison RL, Morrissey JH.
Biochemistry 52(33):5545-52. doi: 10.1021/bi4006368. Epub 2013 Aug 7. 2013
Endothelial cell protein C receptor-mediated redistribution and tissue-level accumulation of factor VIIa.
Clark CA, Vatsyayan R, Hedner U, Esmon CT, Pendurthi UR, Rao LV.
J Thromb Haemost 10(11):2383-91. doi: 10.1111/j.1538-7836.2012.04917.x. 2012
Influence of endothelial cell protein C receptor on plasma clearance of factor VIIa.
Gopalakrishnan R, Pendurthi UR, Hedner U, Agersų H, Esmon CT, Rao LV.
J Thromb Haemost 10(5):971-3. doi: 10.1111/j.1538-7836.2012.04670.x. No abstract available. 2012
Molecular mechanism of dysfunctional factor VII associated with the homozygous missense mutation 331Gly to Ser.
Takamiya O, Kimura S.
Thromb Haemost 93(3):414-9. 2005
ARP1 interacts with the 5' flanking region of the coagulation factor VII gene.
Carew JA, Jackson AA, Bauer KA.
J Thromb Haemost 1(6):1220-7. 2003
Oestrogenic repression of human coagulation factor VII expression mediated through an oestrogen response element sequence motif in the promoter region.
Di Bitondo R, Hall AJ, Peake IR, Iacoviello L, Winship PR.
Hum Mol Genet 11(7):723-31. 2002
Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency.
Giansily-Blaizot M, Aguilar-Martinez P, Biron-Andreani C, Jeanjean P, Igual H, Schved JF.
Eur J Hum Genet 9(2):105-12. 2001
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.
Girelli D, Russo C, Ferraresi P, Olivieri O, Pinotti M, Friso S, Manzato F, Mazzucco A, Bernardi F, Corrocher R.
N Engl J Med 343(11):774-80. 2000
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 107(4):327-42. 2000
Characterization of two naturally occurring mutations in the second epidermal growth factor-like domain of factor VII.
Hunault M, et al.
Blood 93(4):1237-44. 1999
Structure of human factor VIIa and its implications for the triggering of blood coagulation.
Pike AC, et al.
Proc Natl Acad Sci U S A 96(16):8925-30. 1999
Factor VII deficiency caused by a structural variant N57D of the first epidermal growth factor domain.
Leonard BJ, Chen Q, Blajchman MA, Ofosu FA, Sridhara S, Yang D, Clarke BJ.
Blood 91(1):142-8. 1998
Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction.
Iacoviello L, Di Castelnuovo A, De Knijff P, D'Orazio A, Amore C, Arboretti R, Kluft C, Benedetta Donati M.
N Engl J Med 338(2):79-85. 1998
Factor VII Morioka (FVII L-26P) : a homozygous missense mutation in the signal sequence identified in a patient with factor VII deficiency.
Ozawa T, et al.
Br J Haematol 101 : 47-49. 1998
Severe factor VII deficiency due to a mutation disrupting a hepatocyte nuclear factor 4 binding site in the factor VII promoter.
Arbini AA, et al.
Blood 89 : 176-182. 1997
Factor VII Toyama (Thr 359 Met) : a homozygous missense mutation causing severe type I deficiency.
Ozawa T, Niiya K, Higuchi W, Sakuragawa N.
Thromb Haemost 78(3):987-9. 1997
A Thr359 Met mutation in factor VII of a patient with a hereditary deficiency causes defective secretion of the molecule.
Arbini AA, et al.
Blood 87 : 5085-5094. 1996
New alleles in F7 VNTR.
De Knijff P, et al.
Hum Mol Genet 3 : 384. 1994
19F7, F10
Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-Val) and X (334Ser-Pro).
Bernardi F, et al.
Hum Mol Genet 3 : 1175-1177. 1994
Factor VII Mie : homozygous asymptomatic type I deficiency caused by an amino acid substitution of his (CAC) for Arg(247) (CGC) in the catalytic domain.
Ohiwa M, et al.
Thromb Haemost 71 : 773-777. 1994
A missense mutation (178Cys-Tyr) and two neutral dimorphisms (115His and 333Ser) in the human coagulation factor VII gene.
Marchetti G, et al.
Hum Mol Genet 2 : 1055-1056. 1993
Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII.
Takamiya O, et al.
Hum Mol Genet 2 : 1355-1359. 1993
A polymorphism in the 5' region of coagulation factor VII gene (F7) caused by an inserted decanucleotide.
Marchetti G, et al.
Hum Genet 90 : 575-576. 1993
Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7).
Marchetti G, et al.
Hum Genet 89 : 497-502. 1992
PCR detection of a repeat polymorphism within the F7 gene.
Marchetti G, et al.
Nucleic Acids Res 19 : 4570. 1991
A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals.
Green F, Kelleher C, Wilkes H, Temple A, Meade T, Humphries S.
Arterioscler Thromb 11(3):540-6. 1991
Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation.
O'Hara PJ, et al.
Proc Natl Acad Sci U S A 84 : 5158-5162. 1987
28F7, F10
Structural genes of coagulation factors VII and X located on 13q34.
Gilgenkrantz S, et al.
Ann Genet 29 : 32-35. 1986
29F7, F7R, F10
Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8.
Grouchy J de, et al.
Hum Genet 66 : 230-233. 1984
30F2, F5TPH, F7, VWF, F10, F11, F12, F13A1, F13B, FG@
The genetics of blood coagulation.
Graham JB, et al.
Adv Hum Genet 13 : 1-65. 1983
31F10, F10D, F7
Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,T(13;Y)(q11;q34).
Pfeiffer RA, et al.
Hum Genet 62 : 358-360. 1982