1 | F10, F10D
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| Molecular defects in the factor X gene caused by novel heterozygous mutations IVS5+1G>A and Asp409del.
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| Zhou JW, Liang Q, Chen Q, Xie Y, Ding QL, Wang XF, Xi XD, Wang HL.
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| Haemophilia 19(1):94-9. doi: 10.1111/j.1365-2516.2012.02933.x. Epub 2012 Aug 29.
2013
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2 | F10
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| F10 gene hypomethylation, a putative biomarker for glioma prognosis.
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| Liu X, Tang H, Wang Z, Huang C, Zhang Z, She X, Wu M, Li G.
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| J Neurooncol 107(3):479-85. doi: 10.1007/s11060-011-0775-2. Epub 2011 Dec 13.
2012
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3 | F10, F10D
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| Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry.
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| Livnat T, Shenkman B, Kenet G, Tamarin I, Gillis S, Varon D, Iijima K, Zivelin A, Salomon O.
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| Blood Coagul Fibrinolysis 22(8):673-9. doi: 10.1097/MBC.0b013e32834ad785.
2011
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4 | F10, LIMK1
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| Coagulation Factor Xa inhibits cancer cell migration via LIMK1-mediated cofilin inactivation.
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| Borensztajn K, Peppelenbosch MP, Spek CA.
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| Thromb Res 125(6):e323-8. doi: 10.1016/j.thromres.2010.02.018. Epub 2010 Mar 26.
2010
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5 | F10, F10D
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| Factor X deficiency.
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| Menegatti M, Peyvandi F.
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| Semin Thromb Hemost 35(4):407-15. doi: 10.1055/s-0029-1225763. Epub 2009 Jul 13. Review.
2009
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6 | F10, F10D
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| 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.
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| Hainmann I, Oldenburg J, Pavlova A, Superti-Furga A, Zieger B.
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| Hamostaseologie 29(2):184-6.
2009
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7 | F10, F10D
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| Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.
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| Chafa O, Tagzirt M, Tapon-Bretaudière J, Reghis A, Fischer AM, LeBonniec BF.
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| Thromb Res 124(1):144-8. doi: 10.1016/j.thromres.2008.11.018. Epub 2009 Jan 10.
2009
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8 | F10, F10D
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| Diagnosis and treatment of inherited factor X deficiency.
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| Brown DL, Kouides PA.
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| Haemophilia 14(6):1176-82. doi: 10.1111/j.1365-2516.2008.01856.x.
2008
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9 | F10, F10D
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| A nonstop mutation in the factor (F)X gene of a severely haemorrhagic patient with complete absence of coagulation FX.
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| Ameri A, Machiah DK, Tran TT, Channell C, Crenshaw V, Fernstrom K, Khachidze M, Duncan A, Fuchs S, Howard TE.
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| Thromb Haemost 98(6):1165-9.
2007
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10 | F10
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| Factor X Shanghai and disruption of translocation to the endoplasmic reticulum.
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| Wang WB, Fu QH, Yin J, Wu WM, Ding QL, Zhou RF, Hu YQ, Wang XF, Wang ZY, Wang HL.
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| Haematologica 90(12):1659-64.
2005
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11 | F10, F10D
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| Lupus anticoagulant associated with transient severe factor X deficiency: a report of two patients presenting with major bleeding complications.
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| Ashrani AA, Aysola A, Al-Khatib H, Nichols WL, Key NS.
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| Br J Haematol 121(4):639-42. 2003
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12 | F10, F10D
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| Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency.
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| Peyvandi F, Menegatti M, Santagostino E, Akhavan S, Uprichard J, Perry DJ, Perkins SJ, Mannucci PM.
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| Br J Haematol 117(3):685-92. 2002
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13 | AT3, F10, F5, PROC, PROS1
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| Genetic risk factors of venous thrombosis.
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| Franco RF, Reitsma PH.
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| Hum Genet 109(4):369-84. Review. 2001
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14 | F10, F10D
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| Molecular analysis of the genotype-phenotype relationship in factor X deficiency.
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| 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.
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| Hum Genet 106(2):249-57. 2000
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15 | F10, F10D
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| A family with hereditary factor X deficiency with a point mutation Gla32 to Gln in the Gla domain (factor X Tokyo).
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| Zama T, Murata M, Watanabe R, Yokoyama K, Moriki T, Ambo H, Murakami H, Kikuchi M, Ikeda Y.
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| Br J Haematol 106(3):809-11 1999
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16 | F10, F10D
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| 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.
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| Hayashi T, et al.
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| Br J Haematol 102 : 926-928. 1998
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17 | F10, F10D
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| 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.
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| Marchetti G, et al.
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| Br J Haematol 90 : 910-915. 1995
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18 | F10
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| Factor Xketchikan : a variant molecule in which Gly replaces a Gla residue at position 14 in the light chain.
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| Kim DJ, et al.
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| Hum Genet 95 : 212-214. 1995
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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).
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| Bernardi F, et al.
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| Hum Mol Genet 3 : 1175-1177. 1994
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20 | F10, F10D, F9, F9D
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| Five novel point mutations : two causing haemophilia B and three causing factor X deficiency.
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| Odom MW, et al.
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| Mol Cell Probes 8 : 63-65. 1994
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21 | F10
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| A NlaIV polymorphism within the human factor X gene.
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| Wallmark A, et al.
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| Nucleic Acids Res 19 : 4022. 1991
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22 | F10
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| Factor X (Santo Domingo). Evidence that the severe clinical phenotype arises from a mutation blocking secretion.
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| Watzke HH, et al.
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| J Clin Invest 88 : 1685-1689. 1991
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23 | F10, F10D
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| Molecular genetic analysis of factor X deficiency : gene deletion and germline mosaicism.
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| Wieland K, et al.
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| Hum Genet 86 : 273-278. 1991
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24 | F10, F10D
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| Molecular defect (Gla+14-Lys) and its functional consequences in a hereditary factor X deficiency (factor X Vorarlberg).
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| Watzke HH, et al.
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| J Biol Chem 265 : 11982-11989. 1990
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25 | F10
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| Partial gene deletion in a family with factor X deficiency.
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| Bernardi F, et al.
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| Blood 73 : 2123-2127. 1989
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26 | F10
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| Multiple polymorphic sites in factor X locus.
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| Hassan HJ, et al.
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| Blood 71 : 1353-1356. 1988
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27 | F10
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| Isolation and chraracterization of human blood-coagulation factor X cDNA.
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| Kaul RK, et al.
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| Gene 41 : 311-314. 1986
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28 | F10, ORM1, ORM2
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| 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.
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| Rocchi M, et al.
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| Hum Genet 74 : 30-33. 1986
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29 | F10
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| The gene for clotting factor 10 is mapped to 13q32-qter.
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| Royle NJ, et al.
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| Cytogenet Cell Genet 41 : 185-188. 1986
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30 | F7, F10
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| 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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31 | F10
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| RFLPs for PstI and EcoRI in the human blood clotting factor X gene.
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| Hay CW, et al.
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| Nucleic Acids Res 14 : 5118. 1986
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32 | F10, PROC
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| Mapping of coagulation factors protein C and factor X on chromosome 2 and 13.
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| Rocchi M, et al.
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| (HGM8) Cytogenet Cell Genet 40 : 734. 1985
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33 | F10
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| The localization of the factor X gene for clotting to chromosome 13.
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| Royle NJ, et al.
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| (HGM8) Cytogenet Cell Genet 40 : 736. 1985
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34 | D13S1, D13S2, D13S3, D13S4, F10
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| Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.
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| Cavenee W, et al.
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| Am J Hum Genet 36 : 10-24. 1984
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35 | F7, F7R, F10
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| Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8.
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| Grouchy J de, et al.
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| Hum Genet 66 : 230-233. 1984
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36 | 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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37 | 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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38 | F10
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| Partial 4q duplication due to inherited der (13)t(4;13)(q26;q34) mat in a girl with a deficiency of factor X.
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| Stoll C, et al.
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| Hum Genet 53 : 303-304. 1980
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