Antonia Minano

Murcia, MU, Spain

Last Updated: 09/26/2026

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Found 48 publications

Functional, biochemical, and clinical characterization of natural mutations affecting arginine residues in the heparin-binding site of antithrombin.

Functional, biochemical, and clinical characterization of natural mutations affecting arginine residues in the heparin-binding site of antithrombin.

Journal: HemaSphere

Published: December 03, 2025

De novo mutations in antithrombin deficiency: high frequency and heterogeneous mechanisms.

De novo mutations in antithrombin deficiency: high frequency and heterogeneous mechanisms.

Journal: Haematologica

Published: August 04, 2025

Factor XI in Carriers of Antiphospholipid Antibodies: Elevated Levels Associated with Symptomatic Thrombotic Cases, While Low Levels Linked to Asymptomatic Cases.

Factor XI in Carriers of Antiphospholipid Antibodies: Elevated Levels Associated with Symptomatic Thrombotic Cases, While Low Levels Linked to Asymptomatic Cases.

Journal: International journal of molecular sciences

Published: October 06, 2023

Congenital factor XI deficiency and risk of heart failure in humans.

Congenital factor XI deficiency and risk of heart failure in humans.

Journal: Journal of thrombosis and haemostasis : JTH

Published: June 06, 2023

Usefulness and Limitations of Multiple Ligation-Dependent Probe Amplification in Antithrombin Deficiency.

Usefulness and Limitations of Multiple Ligation-Dependent Probe Amplification in Antithrombin Deficiency.

Journal: International journal of molecular sciences

Published: February 10, 2023

Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing.

Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing.

Journal: Journal of thrombosis and haemostasis : JTH

Published: December 23, 2022

Functional, biochemical, molecular and clinical characterization of antithrombin c.1157T>C (p.Ile386Thr), a recurrent Polish variant with a founder effect.

Functional, biochemical, molecular and clinical characterization of antithrombin c.1157T>C (p.Ile386Thr), a recurrent Polish variant with a founder effect.

Journal: Haematologica

Published: November 22, 2022

Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency.

Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency.

Journal: Thrombosis and haemostasis

Published: June 28, 2022

Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect.

Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect.

Journal: JCI insight

Published: April 28, 2022

Contact pathway in surgical and transcatheter aortic valve replacement.

Contact pathway in surgical and transcatheter aortic valve replacement.

Journal: Frontiers in cardiovascular medicine

Published: March 01, 2022

Molecular and clinical characterization of transient antithrombin deficiency: A new concept in congenital thrombophilia.

Molecular and clinical characterization of transient antithrombin deficiency: A new concept in congenital thrombophilia.

Journal: American journal of hematology

Published: November 09, 2021

Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays.

Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays.

Journal: Blood

Published: November 08, 2021

Showing 1-12 of 48

Last Updated: 09/26/2026