Citations for
1F10, F10D
Molecular defects in the factor X gene caused by novel heterozygous mutations IVS5+1G>A and Asp409del.
Zhou JW, Liang Q, Chen Q, Xie Y, Ding QL, Wang XF, Xi XD, Wang HL.
Haemophilia 19(1):94-9. doi: 10.1111/j.1365-2516.2012.02933.x. Epub 2012 Aug 29. 2013
2F10
F10 gene hypomethylation, a putative biomarker for glioma prognosis.
Liu X, Tang H, Wang Z, Huang C, Zhang Z, She X, Wu M, Li G.
J Neurooncol 107(3):479-85. doi: 10.1007/s11060-011-0775-2. Epub 2011 Dec 13. 2012
3F10, F10D
Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry.
Livnat T, Shenkman B, Kenet G, Tamarin I, Gillis S, Varon D, Iijima K, Zivelin A, Salomon O.
Blood Coagul Fibrinolysis 22(8):673-9. doi: 10.1097/MBC.0b013e32834ad785. 2011
4F10, LIMK1
Coagulation Factor Xa inhibits cancer cell migration via LIMK1-mediated cofilin inactivation.
Borensztajn K, Peppelenbosch MP, Spek CA.
Thromb Res 125(6):e323-8. doi: 10.1016/j.thromres.2010.02.018. Epub 2010 Mar 26. 2010
5F10, F10D
Factor X deficiency.
Menegatti M, Peyvandi F.
Semin Thromb Hemost 35(4):407-15. doi: 10.1055/s-0029-1225763. Epub 2009 Jul 13. Review. 2009
6F10, F10D
Identification of a novel factor X deletion in combination with a missense mutation in the F10 gene - Genotype-phenotype correlation in a girl with severe factor X deficiency.
Hainmann I, Oldenburg J, Pavlova A, Superti-Furga A, Zieger B.
Hamostaseologie 29(2):184-6. 2009
7F10, F10D
Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.
Chafa O, Tagzirt M, Tapon-Bretaudière J, Reghis A, Fischer AM, LeBonniec BF.
Thromb Res 124(1):144-8. doi: 10.1016/j.thromres.2008.11.018. Epub 2009 Jan 10. 2009
8F10, F10D
Diagnosis and treatment of inherited factor X deficiency.
Brown DL, Kouides PA.
Haemophilia 14(6):1176-82. doi: 10.1111/j.1365-2516.2008.01856.x. 2008
9F10, F10D
A nonstop mutation in the factor (F)X gene of a severely haemorrhagic patient with complete absence of coagulation FX.
Ameri A, Machiah DK, Tran TT, Channell C, Crenshaw V, Fernstrom K, Khachidze M, Duncan A, Fuchs S, Howard TE.
Thromb Haemost 98(6):1165-9. 2007
10F10
Factor X Shanghai and disruption of translocation to the endoplasmic reticulum.
Wang WB, Fu QH, Yin J, Wu WM, Ding QL, Zhou RF, Hu YQ, Wang XF, Wang ZY, Wang HL.
Haematologica 90(12):1659-64. 2005
11F10, F10D
Lupus anticoagulant associated with transient severe factor X deficiency: a report of two patients presenting with major bleeding complications.
Ashrani AA, Aysola A, Al-Khatib H, Nichols WL, Key NS.
Br J Haematol 121(4):639-42. 2003
12F10, F10D
Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency.
Peyvandi F, Menegatti M, Santagostino E, Akhavan S, Uprichard J, Perry DJ, Perkins SJ, Mannucci PM.
Br J Haematol 117(3):685-92. 2002
13AT3, F10, F5, PROC, PROS1
Genetic risk factors of venous thrombosis.
Franco RF, Reitsma PH.
Hum Genet 109(4):369-84. Review. 2001
14F10, F10D
Molecular analysis of the genotype-phenotype relationship in factor X deficiency.
Millar DS, Elliston L, Deex P, Krawczak M, Wacey AI, Reynaud J, Nieuwenhuis HK, Bolton-Maggs P, Mannucci PM, Reverter JC, Cachia P, Pasi KJ, Layton DM, Cooper DN.
Hum Genet 106(2):249-57. 2000
15F10, F10D
A family with hereditary factor X deficiency with a point mutation Gla32 to Gln in the Gla domain (factor X Tokyo).
Zama T, Murata M, Watanabe R, Yokoyama K, Moriki T, Ambo H, Murakami H, Kikuchi M, Ikeda Y.
Br J Haematol 106(3):809-11 1999
16F10, F10D
Molecular abnormality observed in a patient with coagulation factor X (FX) deficiency : a novel three-base-pair (CTT) deletion within the polypyrimidine tract of the FX intron D.
Hayashi T, et al.
Br J Haematol 102 : 926-928. 1998
17F10, F10D
Molecular bases of CRM+ factor X deficiency : a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain.
Marchetti G, et al.
Br J Haematol 90 : 910-915. 1995
18F10
Factor Xketchikan : a variant molecule in which Gly replaces a Gla residue at position 14 in the light chain.
Kim DJ, et al.
Hum Genet 95 : 212-214. 1995
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
20F10, F10D, F9, F9D
Five novel point mutations : two causing haemophilia B and three causing factor X deficiency.
Odom MW, et al.
Mol Cell Probes 8 : 63-65. 1994
21F10
A NlaIV polymorphism within the human factor X gene.
Wallmark A, et al.
Nucleic Acids Res 19 : 4022. 1991
22F10
Factor X (Santo Domingo). Evidence that the severe clinical phenotype arises from a mutation blocking secretion.
Watzke HH, et al.
J Clin Invest 88 : 1685-1689. 1991
23F10, F10D
Molecular genetic analysis of factor X deficiency : gene deletion and germline mosaicism.
Wieland K, et al.
Hum Genet 86 : 273-278. 1991
24F10, F10D
Molecular defect (Gla+14-Lys) and its functional consequences in a hereditary factor X deficiency (factor X Vorarlberg).
Watzke HH, et al.
J Biol Chem 265 : 11982-11989. 1990
25F10
Partial gene deletion in a family with factor X deficiency.
Bernardi F, et al.
Blood 73 : 2123-2127. 1989
26F10
Multiple polymorphic sites in factor X locus.
Hassan HJ, et al.
Blood 71 : 1353-1356. 1988
27F10
Isolation and chraracterization of human blood-coagulation factor X cDNA.
Kaul RK, et al.
Gene 41 : 311-314. 1986
28F10, ORM1, ORM2
Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha1-acid glycoprotein to chromosome 9.
Rocchi M, et al.
Hum Genet 74 : 30-33. 1986
29F10
The gene for clotting factor 10 is mapped to 13q32-qter.
Royle NJ, et al.
Cytogenet Cell Genet 41 : 185-188. 1986
30F7, F10
Structural genes of coagulation factors VII and X located on 13q34.
Gilgenkrantz S, et al.
Ann Genet 29 : 32-35. 1986
31F10
RFLPs for PstI and EcoRI in the human blood clotting factor X gene.
Hay CW, et al.
Nucleic Acids Res 14 : 5118. 1986
32F10, PROC
Mapping of coagulation factors protein C and factor X on chromosome 2 and 13.
Rocchi M, et al.
(HGM8) Cytogenet Cell Genet 40 : 734. 1985
33F10
The localization of the factor X gene for clotting to chromosome 13.
Royle NJ, et al.
(HGM8) Cytogenet Cell Genet 40 : 736. 1985
34D13S1, D13S2, D13S3, D13S4, F10
Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.
Cavenee W, et al.
Am J Hum Genet 36 : 10-24. 1984
35F7, 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
36F2, 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
37F10, 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
38F10
Partial 4q duplication due to inherited der (13)t(4;13)(q26;q34) mat in a girl with a deficiency of factor X.
Stoll C, et al.
Hum Genet 53 : 303-304. 1980