| Clinical Profile of Congenital Factor XIII Deficiency in Children. | Clinical Profile of Congenital Factor XIII Deficiency in Children.
Nadakuditi NK, Peters EF, Subramanian S, Prakash A. | 02/16/2024 |
| Reciprocal stabilization of coagulation factor XIII-A and -B subunits is a determinant of plasma FXIII concentration. | Reciprocal stabilization of coagulation factor XIII-A and -B subunits is a determinant of plasma FXIII concentration.
Byrnes JR, Lee T, Sharaby S, Campbell RA, Dobson DA, Holle LA, Luo M, Kangro K, Homeister JW, Aleman MM, Luyendyk JP, Kerlin BA, Dumond JB, Wolberg AS., | 02/6/2024 |
| Linking inflammation and angiogenesis with fibrogenesis: Expression of FXIIIA, MMP-9, and VEGF in oral submucous fibrosis. | Linking inflammation and angiogenesis with fibrogenesis: Expression of FXIIIA, MMP-9, and VEGF in oral submucous fibrosis.
Choudhari S, Kulkarni D, Patankar S, Kheur S, Sarode S. | 01/29/2024 |
| Cellular FXIII in Human Macrophage-Derived Foam Cells. | Cellular FXIII in Human Macrophage-Derived Foam Cells.
Somodi L, Horváth E, Bárdos H, Baráth B, Pethő D, Katona É, Balla J, Mutch NJ, Muszbek L., Free PMC Article | 10/28/2023 |
| Macrophages-derived Factor XIII links coagulation to inflammation in COPD. | Macrophages-derived Factor XIII links coagulation to inflammation in COPD.
Bazzan E, Casara A, Radu CM, Tinè M, Biondini D, Faccioli E, Pezzuto F, Bernardinello N, Conti M, Balestro E, Calabrese F, Simioni P, Rea F, Turato G, Spagnolo P, Cosio MG, Saetta M., Free PMC Article | 05/23/2023 |
| MicroRNA 155, Factor XIII and Type 2 Diabetes Mellitus and Coronary Heart Disease. | MicroRNA 155, Factor XIII and Type 2 Diabetes Mellitus and Coronary Heart Disease.
Ntanyane Phasha MA, Soma P, Rooy MV, Phulukdaree A. | 05/17/2023 |
| [Gene diagnosis of a family with coagulation factor deficiency caused by large deletion of F13A1 gene]. | [Gene diagnosis of a family with coagulation factor ⅩⅢ deficiency caused by large deletion of F13A1 gene].
Cheng YL, Ding ZX, Cao LJ, Han JJ, Su J, Gao GY, Yu ZQ, Bai X, Wang ZY, Ruan CG., Free PMC Article | 03/30/2023 |
| Genetic Background of Inherited Factor XIII-A Subunit Deficiency: Review of the Literature and Description of Two New Cases. | Genetic Background of Inherited Factor XIII-A Subunit Deficiency: Review of the Literature and Description of Two New Cases.
Plamenova I, Zolkova J, Sokol J, Kolkova Z, Bereczky Z, Katona E, Muszbek L, Kubisz P, Stasko J. | 05/14/2022 |
| Fibrinogen beta chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism. | Fibrinogen β chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism.
Klajmon A, Chmiel J, Ząbczyk M, Pociask E, Wypasek E, Malinowski KP, Undas A, Natorska J. | 03/19/2022 |
| F13A1 transglutaminase expression in human adipose tissue increases in acquired excess weight and associates with inflammatory status of adipocytes. | F13A1 transglutaminase expression in human adipose tissue increases in acquired excess weight and associates with inflammatory status of adipocytes.
Kaartinen MT, Arora M, Heinonen S, Hang A, Barry A, Lundbom J, Hakkarainen A, Lundholm N, Rissanen A, Kaprio J, Pietiläinen KH. | 01/29/2022 |
| Decreased clot burden is associated with factor XIII Val34Leu polymorphism and better functional outcomes in acute ischemic stroke patients treated with intravenous thrombolysis. | Decreased clot burden is associated with factor XIII Val34Leu polymorphism and better functional outcomes in acute ischemic stroke patients treated with intravenous thrombolysis.
Szegedi I, Orbán-Kálmándi R, Nagy A, Sarkady F, Vasas N, Sik M, Lánczi LI, Berényi E, Oláh L, Crișan A, Csiba L, Bagoly Z., Free PMC Article | 01/15/2022 |
| Molecular Analysis of Prothrombotic Gene Variants in Patients with Acute Ischemic Stroke and with Transient Ischemic Attack. | Molecular Analysis of Prothrombotic Gene Variants in Patients with Acute Ischemic Stroke and with Transient Ischemic Attack.
Cernera G, Comegna M, Gelzo M, Savoia M, Bruzzese D, Mormile M, Zarrilli F, Amato F, Micco PD, Castaldo G., Free PMC Article | 08/14/2021 |
| Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management. | Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management.
Moret A, Zúñiga Á, Ayala JM, Liquori A, Cid AR, Haya S, Ferrando F, Blanquer A, Cervera J, Bonanad S. | 08/7/2021 |
| Combinations of fibrinolytic gene polymorphisms (plasminogen activator inhibitor type 1 4G/5G, factor XIII Val34Leu and angiotensin-converting enzyme I/D) in women with idiopathic infertility. | Combinations of fibrinolytic gene polymorphisms (plasminogen activator inhibitor type 1 4G/5G, factor XIII Val34Leu and angiotensin-converting enzyme I/D) in women with idiopathic infertility.
Velickovic J, Jelicic M, Stojkovic O. | 05/29/2021 |
| Role, Laboratory Assessment and Clinical Relevance of Fibrin, Factor XIII and Endogenous Fibrinolysis in Arterial and Venous Thrombosis. | Role, Laboratory Assessment and Clinical Relevance of Fibrin, Factor XIII and Endogenous Fibrinolysis in Arterial and Venous Thrombosis.
Memtsas VP, Arachchillage DRJ, Gorog DA., Free PMC Article | 04/17/2021 |
| Expression, Purification and Characterization of Recombinant Human Coagulation Factor XIIIa in Pichia Pastoris. | Expression, Purification and Characterization of Recombinant Human Coagulation Factor XIIIa in Pichia Pastoris.
Cheng L, Zhang T, Fei Y, Shen H, Huang H, Chen J, Xu B, Xu J. | 04/3/2021 |
| Post-Translational Modifications of Platelet-Derived Amyloid Precursor Protein by Coagulation Factor XIII-A. | Post-Translational Modifications of Platelet-Derived Amyloid Precursor Protein by Coagulation Factor XIII-A.
Hur WS, Juang LJ, Mazinani N, Munro L, Jefferies WA, Kastrup CJ. | 03/28/2021 |
| Transglutaminases and Obesity in Humans: Association of F13A1 to Adipocyte Hypertrophy and Adipose Tissue Immune Response. | Transglutaminases and Obesity in Humans: Association of F13A1 to Adipocyte Hypertrophy and Adipose Tissue Immune Response.
Kaartinen MT, Arora M, Heinonen S, Rissanen A, Kaprio J, Pietiläinen KH., Free PMC Article | 03/13/2021 |
| Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple Dermatofibromas. | Coagulation Factor XIII-A Subunit Missense Mutation in the Pathobiology of Autosomal Dominant Multiple Dermatofibromas.
Supsrisunjai C, Hsu CK, Michael M, Duval C, Lee JYW, Yang HS, Huang HY, Chaikul T, Onoufriadis A, Steiner RA, Ariëns RAS, Sarig O, Sprecher E, Eskin-Schwartz M, Samlaska C, Simpson MA, Calonje E, Parsons M, McGrath JA. | 11/21/2020 |
| Structure functional insights into calcium binding during the activation of coagulation factor XIII A. | Structure functional insights into calcium binding during the activation of coagulation factor XIII A.
Singh S, Dodt J, Volkers P, Hethershaw E, Philippou H, Ivaskevicius V, Imhof D, Oldenburg J, Biswas A., Free PMC Article | 10/24/2020 |
| analysis of molecular organization of FXIII | Factor XIII topology: organization of B subunits and changes with activation studied with single-molecule atomic force microscopy.
Protopopova AD, Ramirez A, Klinov DV, Litvinov RI, Weisel JW., Free PMC Article | 07/11/2020 |
| F13A promoter methylation status was significantly associated with risk of aneurysmal subarachnoid haemorrhage in male patients, but had no significant association with outcome after aSAH. | Prognostic significance of factor XIIIA promoter methylation status in aneurysmal subarachnoid haemorrhage (aSAH).
Arati S, Chetan GK, Sibin MK, Bhat DI, Vazhayil V, Narasingarao KVL., Free PMC Article | 05/23/2020 |
| Discussion of the link between underlying mechanisms of type 2 diabetes mellitus, well known FXIII-A variants and coagulation (review). | Coagulopathy in Type 2 Diabetes Mellitus: Pathological Mechanisms and the Role of Factor XIII-A Single Nucleotide Polymorphisms.
Phasha MN, Soma P, Pretorius E, Phulukdaree A. | 05/9/2020 |
| Review and meta-analysis: In children with Arterial Ischemic Stroke, the PAI-1 and FXIII polymorphisms are not risk factors for the disease.[Systematic Review and Meta-Analysis] | Lack of Associations Between PAI-1 and FXIII Polymorphisms and Arterial Ischemic Stroke in Children: A Systematic Review and Meta-Analysis.
Sarecka-Hujar B, Kopyta I, Skrzypek M., Free PMC Article | 03/14/2020 |
| To identify the underlying molecular mechanism, we assessed her family members and found a novel deep intronic mutation of F13A1 through next-generation sequencing (NGS). Meanwhile, we found nearly no corresponding mRNA expression through RNA sequencing (RNA-Seq) | Novel deep intronic mutation in the coagulation factor XIII a chain gene leading to unexpected RNA splicing in a patient with factor XIII deficiency.
Deng J, Li D, Mei H, Tang L, Wang HF, Hu Y., Free PMC Article | 03/7/2020 |