(Q34095663)

English

Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from families with mixed type I/III protein S deficiency

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

retracted paper

1 reference

Retraction Watch

29 December 2023

https://doi.org/10.3324/haematol.2009.021923

Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from families with mixed type I/III protein S deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

0 references

protein S deficiency

1 reference

based on heuristic

inferred from title

author name string

Elisabetta Castoldi

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Lisbeth F A Maurissen

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Daniela Tormene

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Luca Spiezia

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Sabrina Gavasso

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Claudia Radu

6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Tilman M Hackeng

7

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Jan Rosing

8

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Paolo Simioni

9

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

26 April 2010

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

95

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1563-1571

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Regulation of coagulation by protein S.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Protein S stimulates inhibition of the tissue factor pathway by tissue factor pathway inhibitor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

The calibrated automated thrombogram (CAT): a universal routine test for hyper- and hypocoagulability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Coagulation, inflammation, and apoptosis: different roles for protein S and the protein S-C4b binding protein complex.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Activated protein C resistance determined with a thrombin generation-based test predicts for venous thrombosis in men and women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Incidence of venous thromboembolism in families with inherited thrombophilia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Recurrent venous thromboembolism in patients with a partial deficiency of protein S.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Protein S and the Regulation of Activated Protein C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Organization of the human protein S genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Reevaluation of total, free, and bound protein S and C4b-binding protein levels in plasma anticoagulated with citrate or hirudin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

5 July 2018

Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 July 2018

Thrombin generation-based assays to measure the activity of the TFPI-protein S pathway in plasma from normal and protein S-deficient individuals.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Molecular basis of protein S deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

The tale of protein S and C4b-binding protein, a story of affection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Effect of oral contraceptives on the anticoagulant activity of protein S in plasma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Protein S type III deficiency is no risk factor for venous and arterial thromboembolism in 168 thrombophilic families: a retrospective study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Difference in absolute risk of venous and arterial thrombosis between familial protein S deficiency type I and type III. Results from a family cohort study to assess the clinical impact of a laboratory test-based classification.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Increased risk of venous thrombosis in carriers of natural anticoagulant deficiencies. Results of the family studies of the Spanish Multicenter Study on Thrombophilia (EMET study).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Free protein S deficiency is a risk factor for venous thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

The APC-independent anticoagulant activity of protein S in plasma is decreased by elevated prothrombin levels due to the prothrombin G20210A mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2930959

28 October 2018

Plasma protein S deficiency in familial thrombotic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Study of a protein S gene polymorphism at DNA and mRNA level in a family with symptomatic protein S deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leiden

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clarification of the Risk for Venous Thrombosis Associated with Hereditary Protein S Deficiency by Investigation of a Large Kindred with a Characterized Gene Defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hormonal state rather than age influences cut-off values of protein S: reevaluation of the thrombotic risk associated with protein S deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coagulation factors and the protein C system as determinants of thrombin generation in a normal population

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association between protein S levels and anticoagulant activity of tissue factor pathway inhibitor type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Re-evaluation of the role of the protein S-C4b binding protein complex in activated protein C-catalyzed factor Va-inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein S enhances the tissue factor pathway inhibitor inhibition of factor Xa but not its inhibition of factor VIIa-tissue factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary and acquired protein S deficiencies are associated with low TFPI levels in plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purified protein S contains multimeric forms with increased APC-independent anticoagulant activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and phenotypic variability between families with hereditary protein S deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cleaved protein S (PS), total PS, free PS, and activated protein C cofactor activity as risk factors for venous thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/20421270

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tale of protein S and C4b-binding protein, a story of affection

1 reference

9 February 2024

https://opencitations.net/index/api/v1/references/10.3324/HAEMATOL.2010.021923

Identifiers

10.3324/HAEMATOL.2010.021923

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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