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Items: 1 to 20 of 319

1.

Proline 36 of the Factor XIII Activation Peptide Plays a Crucial Role in Substrate Recognition and Zymogen Activation.

Li B, Billur R, Maurer MC, Kohler HP, Raddatz Müller P, Alberio L, Schroeder V.

Thromb Haemost. 2018 Dec;118(12):2037-2045. doi: 10.1055/s-0038-1675600. Epub 2018 Nov 12.

PMID:
30419598
2.

F13A1 Gene Variant (V34L) and Residual Circulating FXIIIA Levels Predict Short- and Long-Term Mortality in Acute Myocardial Infarction after Coronary Angioplasty.

Ansani L, Marchesini J, Pestelli G, Luisi GA, Scillitani G, Longo G, Milani D, Serino ML, Tisato V, Gemmati D.

Int J Mol Sci. 2018 Sep 14;19(9). pii: E2766. doi: 10.3390/ijms19092766.

3.

Factor XIIIA-expressing inflammatory monocytes promote lung squamous cancer through fibrin cross-linking.

Porrello A, Leslie PL, Harrison EB, Gorentla BK, Kattula S, Ghosh SK, Azam SH, Holtzhausen A, Chao YL, Hayward MC, Waugh TA, Bae S, Godfrey V, Randell SH, Oderup C, Makowski L, Weiss J, Wilkerson MD, Hayes DN, Earp HS, Baldwin AS, Wolberg AS, Pecot CV.

Nat Commun. 2018 May 18;9(1):1988. doi: 10.1038/s41467-018-04355-w.

4.

Human Fetal β Islets Express Coagulation Factor XIII-A and Proteases Suggesting Amphicrine Regulation to Facilitate Islet Fusion.

Lee I.

Pancreas. 2018 Mar;47(3):e6-e7. doi: 10.1097/MPA.0000000000000996. No abstract available.

PMID:
29424810
5.

Evaluation and comparison of staining patterns of factor XIIIa (AC-1A1), adipophilin and GATA3 in sebaceous neoplasia.

Tjarks BJ, Pownell BR, Evans C, Thompson PA, Kerkvliet AM, Koch MRD, Jassim AD.

J Cutan Pathol. 2018 Jan;45(1):1-7. doi: 10.1111/cup.13037. Epub 2017 Sep 19.

PMID:
28873247
6.

Association of the F13A1 Val34Leu polymorphism and recurrent pregnancy loss: A meta-analysis.

Jung JH, Kim JH, Song GG, Choi SJ.

Eur J Obstet Gynecol Reprod Biol. 2017 Aug;215:234-240. doi: 10.1016/j.ejogrb.2017.06.032. Epub 2017 Jun 23.

PMID:
28683377
7.

Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2.

Ivaškevičius V, Biswas A, Garly ML, Oldenburg J.

Haemophilia. 2017 May;23(3):e194-e203. doi: 10.1111/hae.13233.

PMID:
28520207
8.

Association of factor XIII Val34Leu polymorphism and coronary artery disease: A meta-analysis.

Jung JH, Song GG, Kim JH, Seo YH, Choi SJ.

Cardiol J. 2017;24(1):74-84. doi: 10.5603/CJ.a2016.0070. Epub 2016 Sep 26. Review.

9.

Novel aspects of platelet factor XIII function.

Mitchell JL, Mutch NJ.

Thromb Res. 2016 May;141 Suppl 2:S17-21. doi: 10.1016/S0049-3848(16)30356-5. Review.

PMID:
27207415
10.

Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations.

Shanbhag S, Ghosh K, Shetty S.

Blood Cells Mol Dis. 2016 Mar;57:81-4. doi: 10.1016/j.bcmd.2016.01.002. Epub 2016 Jan 13.

PMID:
26852661
11.

Neoplasm-induced bleeding in inherited, heterozygous FXIII-A deficiency.

Ivaškevičius V, Goldmann G, Biswas A, Westhofen P, Thomas A, Marquardt N, Horneff S, Klein C, Rühl H, Pötzsch B, Oldenburg J.

Hamostaseologie. 2015;35 Suppl 1:S32-5.

PMID:
26540128
12.

Blood coagulation factor XIII-A subunit Val34Leu polymorphisms and intracerebral hemorrhage risk: A meta-analysis of case-control studies.

Ma J, Li H, You C, Liu Y, Ma L, Huang S.

Br J Neurosurg. 2015;29(5):672-7. doi: 10.3109/02688697.2015.1054344. Epub 2015 Jun 29. Review.

PMID:
26121426
13.

The activation peptide of coagulation factor XIII is vital for its expression and stability.

Handrkova H, Schroeder V, Kohler HP.

J Thromb Haemost. 2015 Aug;13(8):1449-58. doi: 10.1111/jth.13035. Epub 2015 Jul 16.

14.

[Factor XIII-A subunit Val34Leu polymorphism and risk of venous thromboembolism in young adults].

Demyanenko AV, Kapustin SI, Soroka VV, Chechulov PV.

Angiol Sosud Khir. 2015;21(2):21-5. Russian.

PMID:
26035561
15.

Factor XIII-A dynamics in acute myocardial infarction: a novel prognostic biomarker?

Gemmati D, Zeri G, Orioli E, Mari R, Moratelli S, Vigliano M, Marchesini J, Grossi ME, Pecoraro A, Cuneo A, Ferrari R, Pinotti M, Serino ML, Ansani L.

Thromb Haemost. 2015 Jul;114(1):123-32. doi: 10.1160/TH14-11-0952. Epub 2015 May 7.

PMID:
25947356
16.

Genetic association between FXIII and β-fibrinogen genes and women with recurrent spontaneous abortion: a meta- analysis.

Li J, Wu H, Chen Y, Wu H, Xu H, Li L.

J Assist Reprod Genet. 2015 May;32(5):817-25. doi: 10.1007/s10815-015-0471-9. Epub 2015 Apr 11.

17.

Rapid immunochromatographic test for detection of anti-factor XIII A subunit antibodies can diagnose 90 % of cases with autoimmune haemorrhaphilia XIII/13.

Osaki T, Sugiyama D, Magari Y, Souri M, Ichinose A.

Thromb Haemost. 2015 Jun;113(6):1347-56. doi: 10.1160/TH14-09-0745. Epub 2015 Mar 5.

PMID:
25740658
18.

Common FXIII and fibrinogen polymorphisms in abdominal aortic aneurysms.

Macrae FL, Evans HL, Bridge KI, Johnson A, Scott DJ, Ariëns RA.

PLoS One. 2014 Nov 10;9(11):e112407. doi: 10.1371/journal.pone.0112407. eCollection 2014.

19.

Dermal dendrocytes FXIIIa+ are essential antigen-presenting cells in indeterminate leprosy.

de Alvarenga Lira ML, Pagliari C, de Lima Silva AA, de Andrade HF Jr, Duarte MI.

Am J Dermatopathol. 2015 Apr;37(4):269-73.

PMID:
25365500
20.

Novel and recurrent mutations in the F13A1 gene in unrelated Korean patients with congenital factor XIII deficiency.

Jang MA, Park YS, Lee KO, Kim HJ.

Blood Coagul Fibrinolysis. 2015 Jan;26(1):46-9. doi: 10.1097/MBC.0000000000000171.

PMID:
25004025

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