| 1 | F7, PROC
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| Factor VII and protein C are phosphatidic acid-binding proteins.
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| Tavoosi N, Smith SA, Davis-Harrison RL, Morrissey JH.
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| Biochemistry 52(33):5545-52. doi: 10.1021/bi4006368. Epub 2013 Aug 7.
2013
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| 2 | F7, PROCR
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| Endothelial cell protein C receptor-mediated redistribution and tissue-level accumulation of factor VIIa.
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| Clark CA, Vatsyayan R, Hedner U, Esmon CT, Pendurthi UR, Rao LV.
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| J Thromb Haemost 10(11):2383-91. doi: 10.1111/j.1538-7836.2012.04917.x.
2012
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| 3 | F7, PROCR
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| Influence of endothelial cell protein C receptor on plasma clearance of factor VIIa.
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| Gopalakrishnan R, Pendurthi UR, Hedner U, Agersų H, Esmon CT, Rao LV.
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| J Thromb Haemost 10(5):971-3. doi: 10.1111/j.1538-7836.2012.04670.x. No abstract available.
2012
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| 4 | F7
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| Molecular mechanism of dysfunctional factor VII associated with the homozygous missense mutation 331Gly to Ser.
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| Takamiya O, Kimura S.
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| Thromb Haemost 93(3):414-9. 2005
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| 5 | ACTR1A, F7
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| ARP1 interacts with the 5' flanking region of the coagulation factor VII gene.
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| Carew JA, Jackson AA, Bauer KA.
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| J Thromb Haemost 1(6):1220-7.
2003
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| 6 | F7
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| Oestrogenic repression of human coagulation factor VII expression mediated through an oestrogen response element sequence motif in the promoter region.
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| Di Bitondo R, Hall AJ, Peake IR, Iacoviello L, Winship PR.
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| Hum Mol Genet 11(7):723-31. 2002
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| 7 | F7
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| Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency.
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| Giansily-Blaizot M, Aguilar-Martinez P, Biron-Andreani C, Jeanjean P, Igual H, Schved JF.
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| Eur J Hum Genet 9(2):105-12. 2001
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| 8 | F7
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| Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.
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| Girelli D, Russo C, Ferraresi P, Olivieri O, Pinotti M, Friso S, Manzato F, Mazzucco A, Bernardi F, Corrocher R.
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| N Engl J Med 343(11):774-80. 2000
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| 9 | F7
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| Molecular analysis of the genotype-phenotype relationship in factor VII deficiency.
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| 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.
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| Hum Genet 107(4):327-42. 2000
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| 10 | F7
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| Characterization of two naturally occurring mutations in the second epidermal growth factor-like domain of factor VII.
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| Hunault M, et al.
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| Blood 93(4):1237-44. 1999
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| 11 | F7
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| Structure of human factor VIIa and its implications for the triggering of blood coagulation.
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| Pike AC, et al.
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| Proc Natl Acad Sci U S A 96(16):8925-30. 1999
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| 12 | F7
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| Factor VII deficiency caused by a structural variant N57D of the first epidermal growth factor domain.
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| Leonard BJ, Chen Q, Blajchman MA, Ofosu FA, Sridhara S, Yang D, Clarke BJ.
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| Blood 91(1):142-8. 1998
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| 13 | F7
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| Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction.
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| Iacoviello L, Di Castelnuovo A, De Knijff P, D'Orazio A, Amore C, Arboretti R, Kluft C, Benedetta Donati M.
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| N Engl J Med 338(2):79-85. 1998
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| 14 | F7
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| Factor VII Morioka (FVII L-26P) : a homozygous missense mutation in the signal sequence identified in a patient with factor VII deficiency.
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| Ozawa T, et al.
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| Br J Haematol 101 : 47-49. 1998
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| 15 | F7
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| Severe factor VII deficiency due to a mutation disrupting a hepatocyte nuclear factor 4 binding site in the factor VII promoter.
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| Arbini AA, et al.
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| Blood 89 : 176-182. 1997
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| 16 | F7
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| Factor VII Toyama (Thr 359 Met) : a homozygous missense mutation causing severe type I deficiency.
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| Ozawa T, Niiya K, Higuchi W, Sakuragawa N.
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| Thromb Haemost 78(3):987-9. 1997
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| 17 | F7
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| A Thr359 Met mutation in factor VII of a patient with a hereditary deficiency causes defective secretion of the molecule.
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| Arbini AA, et al.
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| Blood 87 : 5085-5094. 1996
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| 18 | F7
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| New alleles in F7 VNTR.
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| De Knijff P, et al.
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| Hum Mol Genet 3 : 384. 1994
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| 19 | F7, F10
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| Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-Val) and X (334Ser-Pro).
|
| Bernardi F, et al.
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| Hum Mol Genet 3 : 1175-1177. 1994
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| 20 | F7
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| 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.
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| Thromb Haemost 71 : 773-777. 1994
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| 21 | F7
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| A missense mutation (178Cys-Tyr) and two neutral dimorphisms (115His and 333Ser) in the human coagulation factor VII gene.
|
| Marchetti G, et al.
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| Hum Mol Genet 2 : 1055-1056. 1993
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| 22 | F7
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| Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII.
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| Takamiya O, et al.
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| Hum Mol Genet 2 : 1355-1359. 1993
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| 23 | F7
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| A polymorphism in the 5' region of coagulation factor VII gene (F7) caused by an inserted decanucleotide.
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| Marchetti G, et al.
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| Hum Genet 90 : 575-576. 1993
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| 24 | F7
|
| Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7).
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| Marchetti G, et al.
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| Hum Genet 89 : 497-502. 1992
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| 25 | F7
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| PCR detection of a repeat polymorphism within the F7 gene.
|
| Marchetti G, et al.
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| Nucleic Acids Res 19 : 4570. 1991
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| 26 | F7
|
| 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.
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| Arterioscler Thromb 11(3):540-6. 1991
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| 27 | F7
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| Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation.
|
| O'Hara PJ, et al.
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| Proc Natl Acad Sci U S A 84 : 5158-5162. 1987
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| 28 | F7, F10
|
| Structural genes of coagulation factors VII and X located on 13q34.
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| Gilgenkrantz S, et al.
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| Ann Genet 29 : 32-35. 1986
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| 29 | F7, F7R, F10
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| Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8.
|
| Grouchy J de, et al.
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| Hum Genet 66 : 230-233. 1984
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| 30 | F2, F5TPH, F7, VWF, F10, F11, F12, F13A1, F13B, FG@
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| The genetics of blood coagulation.
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| Graham JB, et al.
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| Adv Hum Genet 13 : 1-65. 1983
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| 31 | F10, F10D, F7
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| 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).
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| Pfeiffer RA, et al.
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| Hum Genet 62 : 358-360. 1982
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