Evidence map›Paper›PMID 22345593›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2012

Critical review of mouse models of venous thrombosis.

Jose A Diaz, Andrea T Obi, Daniel D Myers, Shirley K Wrobleski, Peter K Henke, Nigel Mackman, Thomas W Wakefield

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

145 citing papers in PubMed.

  1. Mouse models to study von Willebrand factor in thrombosis: a scoping review.Research and practice in thrombosis and haemostasis · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Antithrombotic Therapy on Antithrombin Resistance in a Mouse Model.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Article
  13. Review
  14. Animal models of antiphospholipid syndrome.Frontiers in immunology · 2026
    Review
  15. Magnetically-Induced Suppression of Oxidative Stress Prevents Venous Thrombosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

85 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Jose A DiazDepartment of Surgery, Conrad Jobst Vascular Research Laboratories, University of Michigan, A570 MSRB II, Dock #6, 1150 W. Medical Center Drive, Ann Arbor, MI 48109-0654, USA. josediaz@med.umich.edu
Andrea T Obi
Daniel D Myers
Shirley K Wrobleski
Peter K Henke
Nigel Mackman
Thomas W Wakefield

Funding

Thrombotic/Fibrinolytic Balance in Cardiac Transplant VasculopathyP01HL089407 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LAWRENCE, DANIEL A · 2008 to 2012
$7.9M
Novel Therapeutic Targets for Venous ThromboembolismR01HL095091 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WAGNER, DENISA D, WAKEFIELD, THOMAS WILLIAM · 2008 to 2012
$3.6M
P-selectin is Central to Venous Thrombosis PathogenesisR01HL070766 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WAKEFIELD, THOMAS WILLIAM · 2002 to 2011
$3.4M
Vascular Surgery: Research Training in Vascular BiologyT32HL076123 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HENKE, PETER K, WAKEFIELD, THOMAS WILLIAM · 2004 to 2019
$1.9M
The Role of IL-6 in Experimental Post Thrombotic SyndromeR01HL132988 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HENKE, PETER K · 2016 to 2019
$1.9M
Vein Wall Fibrotic Injury After DVT is SLC-CCR7 DependentR01HL092129 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HENKE, PETER K · 2009 to 2012
$1.5M
Vein wall remodeling after DVT is matrix metalloproteinase dependentR01HL083918 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HENKE, PETER K · 2006 to 2009
$1.4M
NHLBI NIH HHS HL070766NHLBI NIH HHS HL076123NHLBI NIH HHS HL083918NHLBI NIH HHS HL089407NHLBI NIH HHS HL092129NHLBI NIH HHS HL095091NHLBI NIH HHS P01 HL089407NHLBI NIH HHS R01 HL070766NHLBI NIH HHS R01 HL083918NHLBI NIH HHS R01 HL092129NHLBI NIH HHS R01 HL095091NHLBI NIH HHS R01 HL132988NHLBI NIH HHS T32 HL076123
6 · The paper itself

Abstract

Deep vein thrombosis and pulmonary embolism are a significant health care concern, representing a major source of mortality and morbidity. In order to understand the pathophysiology of thrombogenesis and thrombus resolution, animal models are necessary. Mouse models of venous thrombosis contribute to our understanding of the initiation, propagation, and resolution of venous thrombus, as well as allow for the evaluation of new pharmaceutical approaches to prophylaxis and treatment of deep vein thrombosis. In this work we review the ferric chloride model, the inferior vena cava ligation model, the inferior vena cava stenosis models, and the electrolytic inferior vena cava model and compare their advantages and disadvantages.

Indexed as

Disease Models, AnimalAnimalsChloridesConstrictionElectrolysisFerric CompoundsLigationMiceVena Cava, InferiorVenous ThrombosisChloridesferric chlorideFerric Compounds

Identifiers

PMID22345593
PMCPMC3292052

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.