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Related Experiment Video

Updated: Jun 13, 2026

Ferric Chloride-induced Murine Thrombosis Models
10:37

Ferric Chloride-induced Murine Thrombosis Models

Published on: September 5, 2016

Tissue factor and thrombosis models.

Colin A Kretz1, Nima Vaezzadeh, Peter L Gross

  • 1Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada.

Arteriosclerosis, Thrombosis, and Vascular Biology
|April 16, 2010
PubMed
Summary
This summary is machine-generated.

Investigating tissue factor (TF) in thrombosis using mouse models is crucial. This review explores TF

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Extracellular Vesicle Tissue Factor Activity Assay
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Last Updated: Jun 13, 2026

Ferric Chloride-induced Murine Thrombosis Models
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Published on: September 5, 2016

A Microfluidic Flow Chamber Model for Platelet Transfusion and Hemostasis Measures Platelet Deposition and Fibrin Formation in Real-time
09:38

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Published on: February 14, 2017

Extracellular Vesicle Tissue Factor Activity Assay
03:53

Extracellular Vesicle Tissue Factor Activity Assay

Published on: December 29, 2023

Area of Science:

  • Hemostasis and Thrombosis Research
  • Vascular Biology
  • Genetic Mouse Models

Background:

  • Tissue factor (TF) plays a critical role in thrombogenesis.
  • TF deficiency is embryonic lethal in mice, necessitating advanced genetic models.
  • TF expression varies across cell types, with controversial roles in platelets and endothelial cells.

Purpose of the Study:

  • To review data from mouse models investigating TF's role in thrombus formation.
  • To delineate the contribution of TF from specific cell types to thrombosis.
  • To develop unifying concepts for future research on TF in vascular injury.

Main Methods:

  • Analysis of existing literature on mouse models of thrombosis.
  • Evaluation of studies using various vascular injury techniques.
  • Consolidation of data to identify model-dependent TF sources.

Main Results:

  • Mouse models are essential for studying TF in thrombosis.
  • TF's contribution to thrombus formation is model-dependent.
  • Rigorous controls are needed to attribute thrombosis to specific TF sources.

Conclusions:

  • Understanding TF's cell-specific roles in thrombosis requires sophisticated mouse models.
  • Future studies should focus on testing unifying concepts derived from model-dependent data.
  • Further research is needed to clarify TF's precise contribution to thrombogenesis in different vascular injury contexts.