Evidence map›Paper›PMID 17985003›Full record

ReviewMolecular medicine (Cambridge, Mass.)

Nonviral vector gene modification of stem cells for myocardial repair.

Husnain K Haider, Ibrahim Elmadbouh, Michel Jean-Baptiste, Muhammad Ashraf

Open access · goldAbstract readReview
In one paragraph

Review in Molecular medicine (Cambridge, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
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

10 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Functional polymers of gene delivery for treatment of myocardial infarct.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Review
  5. Review
  6. Polymer transfected primary myoblasts mediated efficient gene expression and angiogenic proliferation.Journal of controlled release : official journal of the Controlled Release Society · 2010
    Article
  7. Review
  8. Review
  9. Angiomyogenesis for myocardial repair.Antioxidants & redox signaling · 2009
    Review
  10. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Husnain K HaiderDepartment of Pathology and Laboratory Medicine, University of Cincinnati, OH 45267-0529, USA.
Ibrahim Elmadbouh
Michel Jean-Baptiste
Muhammad Ashraf
University of Cincinnati · USInserm · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic angiogenesis and myogenesis restore perfusion of ischemic myocardium and improve left ventricular contractility. These therapeutic modalities must be considered as complementary rather than competing to exploit their advantages for optimal beneficial effects. The resistant nature of cardiomyocytes to gene transfection can be overcome by ex vivo delivery of therapeutic genes to the heart using genetically modified stem cells. This review article gives an overview of different vectors and delivery systems in general used for therapeutic gene delivery to the heart and provides a critical appreciation of the ex vivo gene delivery approach using genetically modified stem cells to achieve angiomyogenesis for the treatment of infarcted heart.

Indexed as

Genetic TherapyGenetic VectorsGene Transfer TechniquesAnimalsCells, CulturedHumansMuscle DevelopmentMyocardial InfarctionMyocardial RevascularizationMyocardiumMyocytes, CardiacNeovascularization, PhysiologicRatsRegenerationStem CellsStem Cell Transplantation

Identifiers

PMID17985003
PMCPMC2055423
OpenAlexW2396644353

What OpenQuestion holds

Textmetadata
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.