Evidence map›Paper›PMID 23371317›Full record

ReviewJournal of molecular medicine (Berlin, Germany)2013

Endothelial progenitor cell: a blood cell by many other names may serve similar functions.

Mervin C Yoder

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Journal of molecular medicine (Berlin, Germany), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing 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

57 citing papers in PubMed.

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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

1 author.

Mervin C YoderHermann B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA. myoder@iupui.edu

Funding

Collagen Cross-links Direct Matrix-Induced Vasculogenesis Via Tunable PathwaysR01HL109602 · NHLBI · PURDUE UNIVERSITY · PI VOYTIK-HARBIN, SHERRY L, YODER, MERVIN C. · 2011 to 2014
$1.5M
NHLBI NIH HHS R01 HL109602
6 · The paper itself

Abstract

The first reports of circulating cells that displayed the capacity to repair and regenerate damaged vascular endothelial cells as progenitor cells for the endothelial lineage (EPC) were met with great enthusiasm. However, the cell surface antigens and colony assays used to identify the putative EPC were soon found to overlap with those of the hematopoietic lineage. Over the past decade, it has become clear that specific hematopoietic subsets play important roles in vascular repair and regeneration. This review will provide some overview of the hematopoietic hierarchy and methods to segregate distinct subsets that may provide clarity in identifying the proangiogenic hematopoietic cells. This review will not discuss those circulating viable endothelial cells that play a role as EPC and are called endothelia colony-forming cells. The review will conclude with identification of some roadblocks to progress in the field of identification of circulating cells that participate in vascular repair and regeneration.

Indexed as

Cell LineageAnimalsBlood CellsEndothelial CellsHematopoiesisHematopoietic Stem CellsHumansMiceNeovascularization, PhysiologicStem Cells

Identifiers

PMID23371317
PMCPMC3704045

What OpenQuestion holds

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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.