Evidence map›Paper›PMID 30704346›Full record

ArticleTissue engineering. Part A2019

CRISPR/Cas9 Edited Induced Pluripotent Stem Cell-Based Vascular Tissues to Model Aging and Disease-Dependent Impairment.

Aylin Acun, Pinar Zorlutuna

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Organ-on-a-Chip: A New Paradigm for Drug Development.Trends in pharmacological sciences · 2021
    Review
  7. Article
  8. Review
  9. Review
  10. Vascular Microphysiological Systems to Model Diseases.Cell & gene therapy insights · 2020
    Article
  11. Review
  12. 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

2 authors.

Aylin Acun1 Bioengineering Graduate Program and University of Notre Dame, Notre Dame, Indiana.
Pinar Zorlutuna1 Bioengineering Graduate Program and University of Notre Dame, Notre Dame, Indiana.

Funding

An integrated human organ-on-chip ultrasensitive miRNA detection platform for novel biomarker discoveryR01HL141909 · NHLBI · UNIVERSITY OF NOTRE DAME · PI ZORLUTUNA, PINAR · 2018 to 2022
$1.9M
NHLBI NIH HHS R01 HL141909
6 · The paper itself

Abstract

impact statementModeling human disease as precisely as possible is of upmost importance in understanding the underlying pathology and discovering effective therapies. Therefore, disease models that are highly controlled and composed of human-origin cells that present the disease phenotype are crucial. The human induced pluripotent stem cell (hiPSC)-based tissue model we present in this study is an important example of human-origin tissue model with controlled gene expression. Through CRISPR/Cas9 editing of hypoxia inducible factor 1α in hiPSCs, we developed tissue models that show the age and disease-dependent endothelial deterioration. This model holds promise for various biomedical applications as more realistic disease phenotypes can be created using fully human-origin platforms.

Indexed as

CRISPR-Cas SystemsModels, CardiovascularAgingCell HypoxiaHumansHuman Umbilical Vein Endothelial CellsHypoxia-Inducible Factor 1, alpha SubunitInduced Pluripotent Stem CellsHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitCRISPR/Cas9disease modelingiPSC

Identifiers

PMID30704346
PMCPMC6535964

What Socratic 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 Socratic graph.