about
A nonsense polymorphism in the protein Z-dependent protease inhibitor increases the risk for venous thrombosisType II antithrombin deficiency caused by a large in-frame insertion: structural, functional and pathological relevanceIncreased N-glycosylation efficiency by generation of an aromatic sequon on N135 of antithrombinGenome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysmGPI-anchor and GPI-anchored protein expression in PMM2-CDG patients.Potential role of miRNAs in developmental haemostasisThe mll-AF9 gene fusion in mice controls myeloproliferation and specifies acute myeloid leukaemogenesis.Antithrombin Murcia (K241E) causing antithrombin deficiency: a possible role for altered glycosylation.Amelioration of the severity of heparin-binding antithrombin mutations by posttranslational mosaicism.Thyroglobulin gene point mutation associated with non-endemic simple goitre.Evaluation of four rapid methods for hemoglobin screening of whole blood donors in mobile collection settings.Polymorphisms in xenobiotic metabolizing genes (EPHX1, NQO1 and PON1) in lymphoma susceptibility: a case control study.An Mll-AF9 fusion gene made by homologous recombination causes acute leukemia in chimeric mice: a method to create fusion oncogenes.Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins?Evaluation of Novel Platelet Polymorphisms in Stroke. Dichotomic Effect of rs5443 in GNB3.Role of the C-sheet in the maturation of N-glycans on antithrombin: functional relevance of pleiotropic mutations.Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.What can Drosophila tell us about serpins, thrombosis and dementia?Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.Heparanase Activates Antithrombin through the Binding to Its Heparin Binding SiteAcute leukemias of different lineages have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation.miR-133a regulates vitamin K 2,3-epoxide reductase complex subunit 1 (VKORC1), a key protein in the vitamin K cycle.Protein Z/Z-dependent protease inhibitor (PZ/ZPI) anticoagulant system and thrombosis.Association of anthracycline-related cardiac histological lesions with NADPH oxidase functional polymorphismsControl of post-translational modifications in antithrombin during murine post-natal development by miR-200aFunctional consequences of the prothrombotic SERPINC1 rs2227589 polymorphism on antithrombin levelsFluctuations in coagulation activity among patients with atrial fibrillation who are stably anticoagulated.Identification of miRNAs as potential modulators of tissue factor expression in patients with systemic lupus erythematosus and antiphospholipid syndrome.Role of lipopolysaccharide and cecal ligation and puncture on blood coagulation and inflammation in sensitive and resistant mice models.Uniparental disomy causes deficiencies of vitamin K-dependent proteins.Heparin affinity of factor VIIa: implications on the physiological inhibition by antithrombin and clearance of recombinant factor VIIa.Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect.Inhibition of proteasome by bortezomib causes intracellular aggregation of hepatic serpins and increases the latent circulating form of antithrombin.Identification of coagulation gene 3'UTR variants that are potentially regulated by microRNAs.L-asparaginase-induced antithrombin type I deficiency: implications for conformational diseases.In vivo effects of hyperthermia on the functional and conformational characteristics of antithrombin.A KpnI RFLP at the human myeloperoxidase locus.Antithrombin controls tumor migration, invasion and angiogenesis by inhibition of enteropeptidase.Disease-causing mutations in the serpin antithrombin reveal a key domain critical for inhibiting protease activities.Transient desialylation in combination with a novel antithrombin deficiency causing a severe and recurrent thrombosis despite anticoagulation therapy
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Javier Corral
@ast
Javier Corral
@en
Javier Corral
@es
Javier Corral
@nl
Javier Corral
@sl
type
label
Javier Corral
@ast
Javier Corral
@en
Javier Corral
@es
Javier Corral
@nl
Javier Corral
@sl
prefLabel
Javier Corral
@ast
Javier Corral
@en
Javier Corral
@es
Javier Corral
@nl
Javier Corral
@sl
P106
P1153
56306137000
P21
P31
P496
0000-0003-0288-1107