Jose Fernandez-Navarro

Murcia, MU, Spain

Last Updated: 09/26/2026

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Found 8 publications

Biochemical and cellular consequences of the antithrombin p.Met1? mutation identified in a severe thrombophilic family.

Biochemical and cellular consequences of the antithrombin p.Met1? mutation identified in a severe thrombophilic family.

Journal: Oncotarget

Published: November 30, 2017

High levels of latent antithrombin in plasma from patients with antithrombin deficiency.

High levels of latent antithrombin in plasma from patients with antithrombin deficiency.

Journal: Thrombosis and haemostasis

Published: November 17, 2016

Antithrombin Dublin (p.Val30Glu): a relatively common variant with moderate thrombosis risk of causing transient antithrombin deficiency.

Antithrombin Dublin (p.Val30Glu): a relatively common variant with moderate thrombosis risk of causing transient antithrombin deficiency.

Journal: Thrombosis and haemostasis

Published: November 13, 2015

Role of the C-sheet in the maturation of N-glycans on antithrombin: functional relevance of pleiotropic mutations.

Role of the C-sheet in the maturation of N-glycans on antithrombin: functional relevance of pleiotropic mutations.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 28, 2013

Type II antithrombin deficiency caused by a large in-frame insertion: structural, functional and pathological relevance.

Type II antithrombin deficiency caused by a large in-frame insertion: structural, functional and pathological relevance.

Journal: Journal of thrombosis and haemostasis : JTH

Published: July 05, 2012

Amelioration of the severity of heparin-binding antithrombin mutations by posttranslational mosaicism.

Amelioration of the severity of heparin-binding antithrombin mutations by posttranslational mosaicism.

Journal: Blood

Published: April 14, 2012

The infective polymerization of conformationally unstable antithrombin mutants may play a role in the clinical severity of antithrombin deficiency.

The infective polymerization of conformationally unstable antithrombin mutants may play a role in the clinical severity of antithrombin deficiency.

Journal: Molecular medicine (Cambridge, Mass.)

Published: January 19, 2012

Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency.

Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency.

Journal: Thrombosis and haemostasis

Published: October 11, 2011

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Last Updated: 09/26/2026