Evidence map›Paper›PMID 23765563›Full record

ReviewStem cell reviews and reports2013

Molecular pathways governing development of vascular endothelial cells from ES/iPS cells.

Keai Sinn Tan, Kiyomi Tamura, Mei I Lai, Abhimanyu Veerakumarasivam, Yoichi Nakanishi, Minetaro Ogawa, Daisuke Sugiyama

Abstract readReview
PubMed Publisher
In one paragraph

Review in Stem cell reviews and reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Direct in vivo reprogramming to relieve tissue ischemia via induced vasculogenesis.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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  12. Reprogramming approaches in cardiovascular regeneration.Current treatment options in cardiovascular medicine · 2014
    Article
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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

7 authors.

Keai Sinn TanARO Center for Translational and Clinical Research, Kyushu University Hospital, Station for Collaborative Research 1, 4 F, 3-1-1 Maidashi, Higashi-Ku, Fukuoka, 812-8582, Japan.
Kiyomi Tamura
Mei I Lai
Abhimanyu Veerakumarasivam
Yoichi Nakanishi
Minetaro Ogawa
Daisuke Sugiyama

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Assembly of complex vascular networks occurs in numerous biological systems through morphogenetic processes such as vasculogenesis, angiogenesis and vascular remodeling. Pluripotent stem cells such as embryonic stem (ES) and induced pluripotent stem (iPS) cells can differentiate into any cell type, including endothelial cells (ECs), and have been extensively used as in vitro models to analyze molecular mechanisms underlying EC generation and differentiation. The emergence of these promising new approaches suggests that ECs could be used in clinical therapy. Much evidence suggests that ES/iPS cell differentiation into ECs in vitro mimics the in vivo vascular morphogenic process. Through sequential steps of maturation, ECs derived from ES/iPS cells can be further differentiated into arterial, venous, capillary and lymphatic ECs, as well as smooth muscle cells. Here, we review EC development from ES/iPS cells with special attention to molecular pathways functioning in EC specification.

Indexed as

Blood VesselsCell DifferentiationEmbryonic Stem CellsEndothelial CellsGene Expression Regulation, DevelopmentalHumansInduced Pluripotent Stem CellsMyocytes, Smooth MuscleSignal Transduction

Identifiers

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.