Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect

Comparison of biological activities of human antithrombins with high-mannose or complex-type nonfucosylated N-linked oligosaccharides

(2016) Tsuyoshi Yamada et al.   GLYCOBIOLOGY

Heavy Alcohol Consumption is Associated with Impaired Endothelial Function:

(2016) Aoi Tanaka et al.   Journal of Atherosclerosis and Thrombosis

Identification and function probing of an antithrombin IIIβ conformation-specific antibody

(2016) Y. Jin et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism

(2015) Marine Germain et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Interactions between N-linked glycosylation and polymerisation of neuroserpin within the endoplasmic reticulum

(2015) Claudia Moriconi et al.   FEBS Journal

A sweet code for glycoprotein folding

(2015) Julio J. Caramelo et al.   FEBS LETTERS

Puzzling questions on antithrombin: Diagnostic limitations and real incidence in venous and arterial thrombosis

(2015) Javier Corral et al.   THROMBOSIS RESEARCH

Inherited risk factors for venous thromboembolism

(2014) Ida Martinelli et al.   Nature Reviews Cardiology

29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype

(2014) Marie-Lorraine Monin et al.   Orphanet Journal of Rare Diseases

Increased N-Glycosylation Efficiency by Generation of an Aromatic Sequon on N135 of Antithrombin

(2014) Sonia Águila et al.   PLoS One

Congenital Disorders of Glycosylation with Emphasis on Cerebellar Involvement

(2014) Rita Barone et al.   SEMINARS IN NEUROLOGY

Ethanol-Induced Impairment in the Biosynthesis of N-Linked Glycosylation

(2013) Michael Welti et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants ofADAMTS13in patients with deep vein thrombosis

(2013) L. A. Lotta et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Thrombotic complications in patients with PMM2-CDG

(2013) M. Linssen et al.   MOLECULAR GENETICS AND METABOLISM

Identification of Antithrombin-Modulating Genes. Role of LARGE, a Gene Encoding a Bifunctional Glycosyltransferase, in the Secretion of Proteins?

(2013) María Eugenia de la Morena-Barrio et al.   PLoS One

Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia

(2012) M. E. DE LA MORENA-BARRIO et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Low borderline plasma levels of antithrombin, protein C and protein S are risk factors for venous thromboembolism

(2012) P. BUCCIARELLI et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Thrombosis from a Prothrombin Mutation Conveying Antithrombin Resistance

(2012) Yuhri Miyawaki et al.   NEW ENGLAND JOURNAL OF MEDICINE

Deficiencies of antithrombin, protein C and protein S – Practical experience in genetic analysis of a large patient cohort

(2012) Michael Caspers et al.   THROMBOSIS AND HAEMOSTASIS

Antithrombin levels and the risk of a first episode of venous thromboembolism. A case-control study

(2012) M. N. D. Di Minno et al.   THROMBOSIS AND HAEMOSTASIS

Age- and Gender-Specific Familial Risks for Venous Thromboembolism

(2011) Bengt Zöller et al.   CIRCULATION

The phenotypic and genetic assessment of antithrombin deficiency

(2011) P. C. COOPER et al.   International Journal of Laboratory Hematology

Molecular basis of antithrombin deficiency

(2011) Daniel Delev et al.   THROMBOSIS AND HAEMOSTASIS

Congenital disorders of glycosylation

(2010) Jaak Jaeken   Annals of the New York Academy of Sciences

Antithrombin Murcia (K241E) causing antithrombin deficiency: a possible role for altered glycosylation

(2010) I. Martinez-Martinez et al.   HAEMATOLOGICA

A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin

(2010) B. K. MAHMOODI et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives

(2009) W. M. Lijfering et al.   BLOOD

X-Linked Thrombophilia with a Mutant Factor IX (Factor IX Padua)

(2009) Paolo Simioni et al.   NEW ENGLAND JOURNAL OF MEDICINE