| 1 | F13A1
|
| Investigating Association of Three Polymorphisms of Coagulation Factor XIII and Recurrent Pregnancy Loss.
|
| Jeddi-Tehrani M, Torabi R, Mohammadzadeh A, Arefi S, Keramatipour M, Zeraati H, Zarnani AH, Akhondi MM, Mahmoudian J, Mahmoudi AR, Zarei S.
|
| Am J Reprod Immunol m J Reprod Immunol. 2010 Apr 12. [Epub ahead of print]PMID: 20384622 2010
|
| 2 | F13A1
|
| Coagulation Factor XIII-A Val34Leu Polymorphism and the Risk of Coronary Artery Disease and Myocardial Infarction in a Chinese Han Population.
|
| Jin G, Feng B, Chen P, Tang O, Wang J, Ma J, Shi Y, Xu G.
|
| Clin Appl Thromb Hemost lin Appl Thromb Hemost. 2010 Mar 8. [Epub ahead of print]PMID: 20211923 2010
|
| 3 | F13A1
|
| Association of coagulation factor XIII-A with Golgi proteins within monocyte-macrophages: implications for subcellular trafficking and secretion.
|
| Cordell PA, Kile BT, Standeven KF, Josefsson EC, Pease RJ, Grant PJ.
|
| Blood 115(13):2674-81. Epub 2010 Jan 19.PMID: 20086247 2010
|
| 4 | F13a1
|
| Novel human pathological mutations. Gene symbol: F13A1. Disease: Factor XIII Deficiency.
|
| Anwar R, Valleley EM, Trinh CH.
|
| Hum Genet 127(1):115-6. No abstract available. PMID: 20108427 2010
|
| 5 | F13A1
|
| Factor XIII Val34Leu polymorphism and ischaemic stroke in patients with patent foramen ovale.
|
| Wypasek E, Stepien E, Pieculewicz M, Podolec P, Undas A.
|
| Thromb Haemost 102(6):1280-2. No abstract available. PMID: 19967163 2009
|
| 6 | F13A1
|
| Factor XIII Deficiency.
|
| Karimi M, Bereczky Z, Cohan N, Muszbek L.
|
| Semin Thromb Hemost 35(4):426-38. Epub 2009 Jul 13. Review.PMID: 19598071 2009
|
| 7 | F13A1
|
| Epistatic and pleiotropic effects of polymorphisms in the fibrinogen and coagulation factor XIII genes on plasma fibrinogen concentration, fibrin gel structure and risk of myocardial infarction.
|
| Mannila MN, Eriksson P, Ericsson CG, Hamsten A, Silveira A.
|
| Thromb Haemost 95(3):420-7.PMID: 16525568 2006
|
| 8 | F13A1
|
| Association between 10 microsatellite markers and nonsyndromic cleft lip palate in the Chilean population.
|
| Blanco R, Suazo J, Santos JL, Paredes M, Sung H, Carreņo H, Jara L.
|
| Cleft Palate Craniofac J 41(2):163-7.PMID: 14989688 2004
|
| 9 | F13A1
|
| A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): a risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases.
|
| Gemmati D, Serino ML, Ongaro A, Tognazzo S, Moratelli S, Resca R, Moretti M, Scapoli GL.
|
| Am J Hematol 67(3):183-8. 2001
|
| 10 | F13A1
|
| Identification of a large deletion, spanning exons 4 to 11 of the human factor XIIIA gene, in a factor XIII-deficient family.
|
| Anwar R, Miloszewski KJ, Markham AF.
|
| Blood 91(1):149-53. 1998
|
| 11 | F13A1
|
| Novel deletion and insertion mutations cause splicing defects, leading to severe reduction in mRNA levels of the A subunit in severe factor XIII deficiency.
|
| Izumi T, et al.
|
| Thromb Haemost 79 : 479-485. 1998
|
| 12 | F13A1
|
| Molecular mechanisms of type II factor XIII deficiency : novel Gly 562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression system.
|
| Takahashi N, et al.
|
| Blood 91 : 2830-2838. 1998
|
| 13 | F13A1
|
| Arg260-Cys mutation in severe factor XIII deficiency : conformational change of the A subunit is predicted by molecular modelling and mechanics.
|
| Ichinose A, et al.
|
| Br J Haematol 101 : 264-272. 1998
|
| 14 | F13A1
|
| A novel Asn344 deletion in the core domain of coagulation factor XIII A subunit : its effects on protein structure and function.
|
| Kangsadalampai S, Chelvanayagam G, Baker RT, Yenchitsomanus P, Pung-amritt P, Mahasandana C, Board PG.
|
| Blood 92 : 481-487. 1998
|
| 15 | F13A1
|
| A novel insertion mutation (1286insC) in exon 9 of the factor XIII-A subunit gene.
|
| Aslam S, Standen GR, Bruce LJ, Gialeraki R, Mandalaki T.
|
| Blood Coagul Fibrinolysis 9 : 441-443. 1998
|
| 16 | F13A1
|
| Splicing and missense mutations in the human FXIIIA gene causing FXIII deficiency : effects of these mutations on FXIIIA RNA processing and protein structure.
|
| Anwar R, Gallivan L, Miloszewski KJ, Markham AF.
|
| Br J Haematol 103 : 425-428. 1998
|
| 17 | F13A1
|
| Structural analysis of a missense mutation (Val414Phe) in the catalytic core domain of the factor XIII(A) subunit.
|
| Aslam S, Yee VC, Narayanan S, Duraisamy G, Standen GR.
|
| Br J Haematol 98(2):346-52. 1997
|
| 18 | F13A1
|
| Four novel mutations in deficiency of coagulation factor XIII : consequences to expression and structure of the A-subunit.
|
| Mikkola H, et al.
|
| Blood 87 : 141-151. 1996
|
| 19 | F13A1
|
| Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene.
|
| Suzuki K, et al.
|
| Hum Genet 98 : 393-395. 1996
|
| 20 | F13A1
|
| New mutations causing the premature termination of translation in the A subunit gene of coagulation factor XIII.
|
| Kangsadalampai S, et al.
|
| Thromb Haemost 76 : 139-142. 1996
|
| 21 | F13A1
|
| Allelic ladder characterization of the short tandem repeat polymorphism located in the 5' flanking region to the human coagulation factor XIII A subunit gene.
|
| Puers C, et al.
|
| Genomics 23 : 260-264. 1994
|
| 22 | F13A1
|
| Deficiency in the A-subunit of coagulation factor XIII : two novel point mutations demonstrate different effects on transcript levels.
|
| Mikkola H, et al.
|
| Blood 84 : 517-525. 1994
|
| 23 | F13A1
|
| Factor XIII Abristol 1 : detection of a nonsense mutation (Arg171-stop codon) in factor XIII A subunit deficiency.
|
| Standen GR, et al.
|
| Br J Haematol 85 : 769-772. 1993
|
| 24 | F13A1
|
| Identification of repeat sequence heterogeneity at the polymorphic short tandem repeat locus HUMTH01(AATG)n and reassignment of alleles in population analysis by using a locus-specific allelic ladder.
|
| Puers C, et al.
|
| Am J Hum Genet 53 : 953-958. 1993
|
| 25 | F13A1
|
| Two genetic defects in a patient with complete deficiency of the b-subunit for coagulation factor XIII.
|
| Hashiguchi T, et al.
|
| Blood 82 : 145-150. 1993
|
| 26 | ARG1, F13A1
|
| Genetic and physical map of 11 short tandem repeat polymorphisms on human chromosome 6.
|
| Wilkie PJ, et al.
|
| Genomics 15 : 225-227. 1993
|
| 27 | F13A1
|
| Identification of a point mutation in factor XIII a subunit deficiency.
|
| Board P, et al.
|
| Blood 80 : 937-941. 1992
|
| 28 | F13A1
|
| Deficiency of coagulation factor XIII a subunit caused by the dinucleotide deletion at the 5' end of exon III.
|
| Kamura T, et al.
|
| J Clin Invest 90 : 315-319. 1992
|
| 29 | F13A1
|
| Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1).
|
| Polymeropoulos MH, et al.
|
| Nucleic Acids Res 19 : 4306. 1991
|
| 30 | F13A1
|
| RFLP in human F13A gene.
|
| Jagadeeswaran P.
|
| Nucleic Acids Res 18 : 1317. 1990
|
| 31 | F13A1
|
| An additional Hindlll polymorphism at the coagulation factor XIIIA locus.
|
| Iodice C, et al.
|
| Nucleic Acids Res 18 : 693. 1990
|
| 32 | F13A1
|
| Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.
|
| Zoghbi HY, et al.
|
| Am J Hum Genet 42 : 877-883. 1988
|
| 33 | F13A1
|
| Analysis for linkage between F13A and three chromosome 6 marker loci : evidence for 6pter : F13A : HLA : GLO1 : cen gene order.
|
| Wong P, et al.
|
| Hum Genet 79 : 228-230. 1988
|
| 34 | F13A1
|
| Localization of the coagulation factor XIII A subunit gene (F13A) to chromosome bands 6p24-p25.
|
| Board PG, et al.
|
| Cytogenet Cell Genet 48 : 25-27. 1988
|
| 35 | F13A1
|
| Localization of the gene for coagulation factor XIII a-chain to chromosome 6 and identification of sites of synthesis.
|
| Weisberg LJ, et al.
|
| J Clin Invest 79 : 649-652. 1987
|
| 36 | F13A1
|
| No evidence for linkage between the loci for coagulation factor XIII-A and HLA.
|
| Nishigaki T, et al.
|
| Hum Genet 72 : 266-267. 1986
|
| 37 | F13A1
|
| Localization of human F12, F13A and ACP1.
|
| Niebuhr E, et al.
|
| (HGM8) Cytogenet Cell Genet 40 : 714. 1985
|
| 38 | F13A1
|
| A structural locus for coagulation factor XIIIA (F13A) is locateddistal to the HLA region on chromosome 6p in man.
|
| Olaisen B, et al.
|
| Am J Hum Genet 37 : 215-220. 1985
|
| 39 | F13A1
|
| Linkage data for the coagulation factor genes FXIIIA and FXIIIB.
|
| Olaisen B, et al.
|
| (HGM7) Cytogenet Cell Genet 37 : 560. 1984
|
| 40 | F13A1
|
| The gene for coagulation factor XIII a subunit (F13A) is distal to HLA on chromosome 6.
|
| Board PG, et al.
|
| Hum Genet 67 : 406-408. 1984
|
| 41 | F2, 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
|
| 42 | F13A1
|
| Biochemical characterization of genetically variant and abnormal blood coagulation of factor XIII deficiency. First description of unstable A subunits.
|
| Castle S, et al.
|
| Br J Haematol 45 : 633-635. 1980
|