Evidence map›Paper›PMID 27941641›Full record

ReviewCells2016

Potential of Induced Pluripotent Stem Cells (iPSCs) for Treating Age-Related Macular Degeneration (AMD).

Mark Fields, Hui Cai, Jie Gong, Lucian Del Priore

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Current Landscape of iPSC Haplobanks.Stem cell reviews and reports · 2024
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Cell Therapy for Age-Related Macular Degeneration: A New Vision for the Bone Marrow?Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Article
  15. Article
  16. 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 1 institution in 1 country.

Mark FieldsDepartment of Ophthalmology and Visual Science, Yale School of Medicine, Yale University, 300 George St., Suite 8100, New Haven, CT 06511, USA. mark.fields@yale.edu.
Hui CaiDepartment of Ophthalmology and Visual Science, Yale School of Medicine, Yale University, 300 George St., Suite 8100, New Haven, CT 06511, USA. huey.cai@yale.edu.
Jie GongDepartment of Ophthalmology and Visual Science, Yale School of Medicine, Yale University, 300 George St., Suite 8100, New Haven, CT 06511, USA. jie.gong@yale.edu.
Lucian Del PrioreDepartment of Ophthalmology and Visual Science, Yale School of Medicine, Yale University, 300 George St., Suite 8100, New Haven, CT 06511, USA. lucian.delpriore@yale.edu.
Yale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The field of stem cell biology has rapidly evolved in the last few decades. In the area of regenerative medicine, clinical applications using stem cells hold the potential to be a powerful tool in the treatment of a wide variety of diseases, in particular, disorders of the eye. Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) are promising technologies that can potentially provide an unlimited source of cells for cell replacement therapy in the treatment of retinal degenerative disorders such as age-related macular degeneration (AMD), Stargardt disease, and other disorders. ESCs and iPSCs have been used to generate retinal pigment epithelium (RPE) cells and their functional behavior has been tested in vitro and in vivo in animal models. Additionally, iPSC-derived RPE cells provide an autologous source of cells for therapeutic use, as well as allow for novel approaches in disease modeling and drug development platforms. Clinical trials are currently testing the safety and efficacy of these cells in patients with AMD. In this review, the current status of iPSC disease modeling of AMD is discussed, as well as the challenges and potential of this technology as a viable option for cell replacement therapy in retinal degeneration.

Indexed as

age-related macular degenerationBruch’s membranedisease modelinginduced pluripotent stem cellretinal pigment epithelium

Identifiers

PMID27941641
PMCPMC5187528
OpenAlexW2560695995

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.