Published in Thromb Haemost on April 01, 2008
Model thrombi formed under flow reveal the role of factor XIII-mediated cross-linking in resistance to fibrinolysis. J Thromb Haemost (2010) 0.96
Proteome analysis of mast cell releasates reveals a role for chymase in the regulation of coagulation factor XIIIA levels via proteolytic degradation. J Allergy Clin Immunol (2016) 0.75
The effect of frequent or occasional dialysis-associated hypotension on survival of patients on maintenance haemodialysis. Nephrol Dial Transplant (2003) 1.90
Factor XIII: a coagulation factor with multiple plasmatic and cellular functions. Physiol Rev (2011) 1.56
Alterations in PACAP-38-like immunoreactivity in the plasma during ictal and interictal periods of migraine patients. Cephalalgia (2013) 1.55
Interaction of factor XIII subunits. Blood (2014) 1.12
New direct and indirect methods for the detection of cyclooxygenase 1 acetylation by aspirin; the lack of aspirin resistance among healthy individuals. Thromb Res (2013) 1.07
Primary carcinoma of the frontal sinus: a case report and a review of literature. Eur Arch Otorhinolaryngol (2007) 0.95
Alteration of cylindrospermopsin production in sulfate- or phosphate-starved cyanobacterium Aphanizomenon ovalisporum. FEMS Microbiol Lett (2006) 0.92
Coincidence of mutations in different connexin genes in Hungarian patients. Int J Mol Med (2007) 0.92
A new mutation in the human pres gene and its effect on prestin function. Int J Mol Med (2007) 0.91
Comparison of dialysis and clinical characteristics of patients with frequent and occasional hemodialysis-associated hypotension. Kidney Blood Press Res (2002) 0.90
Epigallocatechin-3-gallate and penta-O-galloyl-β-D-glucose inhibit protein phosphatase-1. FEBS J (2012) 0.85
Severe coagulation factor V deficiency caused by 2 novel frameshift mutations: 2952delT in exon 13 and 5493insG in exon 16 of factor 5 gene. Blood (2002) 0.85
Temporal heterogeneity of endothelium-dependent and -independent dilatation of brachial artery in patients with coronary artery disease. Int J Cardiovasc Imaging (2002) 0.85
Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family. BMC Med Genet (2008) 0.85
Severe bleeding complications caused by an autoantibody against the B subunit of plasma factor XIII: a novel form of acquired factor XIII deficiency. Blood (2008) 0.84
Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas. Eur J Endocrinol (2009) 0.84
Diazo transfer-click reaction route to new, lipophilic teicoplanin and ristocetin aglycon derivatives with high antibacterial and anti-influenza virus activity: an aggregation and receptor binding study. J Med Chem (2009) 0.83
Thrombomodulin-dependent effect of factor VLeiden mutation on factor XIII activation. Thromb Res (2011) 0.83
Cortical and subcortical atrophy in Alzheimer disease: parallel atrophy of thalamus and hippocampus. Alzheimer Dis Assoc Disord (2014) 0.83
Antithrombin deficiency and its laboratory diagnosis. Clin Chem Lab Med (2010) 0.83
Activating BRAF V600E mutation in aggressive pediatric Langerhans cell histiocytosis: demonstration by allele-specific PCR/direct sequencing and immunohistochemistry. Am J Surg Pathol (2014) 0.83
Down-regulation of activated factor XIII by polymorphonuclear granulocyte proteases within fibrin clot. Thromb Haemost (2007) 0.81
The pattern of diffusion parameter changes in Alzheimer's disease, identified by means of linked independent component analysis. J Alzheimers Dis (2013) 0.81
Palmarumycins BG1-BG7 and preussomerin BG1: establishment of their absolute configurations using theoretical calculations of electronic circular dichroism spectra. J Org Chem (2011) 0.80
GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary. Hum Mutat (2004) 0.79
Primary uterine NK-cell lymphoma, nasal-type: a unique malignancy of a prominent cell type of the endometrium. Pathol Oncol Res (2011) 0.79
Analysis and identification of ADP-ribosylated proteins of Streptomyces coelicolor M145. J Microbiol (2009) 0.79
Tetrodotoxin blocks L-type Ca2+ channels in canine ventricular cardiomyocytes. Pflugers Arch (2012) 0.79
TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis. Mol Vis (2007) 0.78
Thrombomodulin-dependent effect of factor V Leiden mutation on the cross-linking of α2-plasmin inhibitor to fibrin and its consequences on fibrinolysis. Thromb Res (2012) 0.78
Nitric oxide mediates T cell cytokine production and signal transduction in histidine decarboxylase knockout mice. J Immunol (2007) 0.78
Grey matter atrophy in patients suffering from multiple sclerosis. Ideggyogy Sz (2014) 0.77
White matter disintegration in cluster headache. J Headache Pain (2013) 0.77
Changes of KRAS Exon 2 Codon 12/13 Mutation Status in Recurrent Colorectal Cancer. Pathol Oncol Res (2014) 0.77
Expression of Xanthophyllomyces dendrorhous cytochrome-P450 hydroxylase and reductase in Mucor circinelloides. World J Microbiol Biotechnol (2014) 0.76
Synthesis, regioselective hydrogenolysis, partial hydrogenation, and conformational study of dioxane and dioxolane-type (9'-anthracenyl)methylene acetals of sugars. Carbohydr Res (2009) 0.76
The combined effect of fibrin formation and factor XIII A subunit Val34Leu polymorphism on the activation of factor XIII in whole plasma. Biochim Biophys Acta (2006) 0.76
Climate Change and European Water Bodies, a Review of Existing Gaps and Future Research Needs: Findings of the ClimateWater Project. Environ Manage (2015) 0.76
A new insight into the zinc-dependent DNA-cleavage by the colicin E7 nuclease: a crystallographic and computational study. Metallomics (2014) 0.76
Dynamic properties of the native free antithrombin from molecular dynamics simulations: computational evidence for solvent- exposed Arg393 side chain. J Biomol Struct Dyn (2014) 0.76
Tetrodotoxin blockade on canine cardiac L-type Ca²⁺ channels depends on pH and redox potential. Mar Drugs (2013) 0.76
Selectivity problems with drugs acting on cardiac Na⁺ and Ca²⁺ channels. Curr Med Chem (2013) 0.76
Crystallization and preliminary crystallographic analysis of an Escherichia coli-selected mutant of the nuclease domain of the metallonuclease colicin E7. Acta Crystallogr Sect F Struct Biol Cryst Commun (2013) 0.75
Three novel germ-line VHL mutations in Hungarian von Hippel-Lindau patients, including a nonsense mutation in a fifteen-year-old boy with renal cell carcinoma. BMC Med Genet (2013) 0.75
Variant type Glanzmann thrombasthenia caused by homozygous p.724R>X mutation in beta3 integrin. Thromb Res (2010) 0.75
Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency. Haematologica (2008) 0.75
A kinetic study on the reductive opening of the diphenylmethylene acetal in methyl 2,3-O-diphenylmethylene-α-L-rhamnopyranoside. Carbohydr Res (2011) 0.75
Inherited factor V deficiency associated with a novel heterozygous missense mutation (p.G493R) in a patient with excessive surgical bleeding. Thromb Haemost (2009) 0.75
Synthesis of disaccharide fragments of the AT-III binding domain of heparin and their sulfonatomethyl analogues. Carbohydr Res (2011) 0.75
Evaluation of indoor radon measurements in Hungary. J Environ Radioact (2006) 0.75
Naturally occurring and disease-associated auto-antibodies against topoisomerase I: a fine epitope mapping study in systemic sclerosis and systemic lupus erythematosus. Int Immunol (2009) 0.75
Heteroduplex analysis using flow cytometric microbead assays to detect deletions, insertions, and single-strand lesions. Cytometry A (2008) 0.75