Citations for
1F13A1
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
2F13A1
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
3F13A1
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
4F13a1
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
5F13A1
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
6F13A1
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
7F13A1
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
8F13A1
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
9F13A1
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
10F13A1
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
11F13A1
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
12F13A1
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
13F13A1
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
14F13A1
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
15F13A1
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
16F13A1
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
17F13A1
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
18F13A1
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
19F13A1
Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene.
Suzuki K, et al.
Hum Genet 98 : 393-395. 1996
20F13A1
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
21F13A1
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
22F13A1
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
23F13A1
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
24F13A1
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
25F13A1
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
26ARG1, F13A1
Genetic and physical map of 11 short tandem repeat polymorphisms on human chromosome 6.
Wilkie PJ, et al.
Genomics 15 : 225-227. 1993
27F13A1
Identification of a point mutation in factor XIII a subunit deficiency.
Board P, et al.
Blood 80 : 937-941. 1992
28F13A1
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
29F13A1
Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1).
Polymeropoulos MH, et al.
Nucleic Acids Res 19 : 4306. 1991
30F13A1
RFLP in human F13A gene.
Jagadeeswaran P.
Nucleic Acids Res 18 : 1317. 1990
31F13A1
An additional Hindlll polymorphism at the coagulation factor XIIIA locus.
Iodice C, et al.
Nucleic Acids Res 18 : 693. 1990
32F13A1
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
33F13A1
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
34F13A1
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
35F13A1
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
36F13A1
No evidence for linkage between the loci for coagulation factor XIII-A and HLA.
Nishigaki T, et al.
Hum Genet 72 : 266-267. 1986
37F13A1
Localization of human F12, F13A and ACP1.
Niebuhr E, et al.
(HGM8) Cytogenet Cell Genet 40 : 714. 1985
38F13A1
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
39F13A1
Linkage data for the coagulation factor genes FXIIIA and FXIIIB.
Olaisen B, et al.
(HGM7) Cytogenet Cell Genet 37 : 560. 1984
40F13A1
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
41F2, 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
42F13A1
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