Evidence map›Paper›PMID 26514199›Full record

ReviewAnnual review of pharmacology and toxicology2016

Clinical Trials in a Dish: The Potential of Pluripotent Stem Cells to Develop Therapies for Neurodegenerative Diseases.

Kelly M Haston, Steven Finkbeiner

Open access · bronzeAbstract readReview
In one paragraph

Review in Annual review of pharmacology and toxicology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Modeling Retinitis Pigmentosa with Patient-Derived iPSCs.Advances in experimental medicine and biology · 2023
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. NeuroinflammatoryFrontiers in pharmacology · 2021
    Review
  20. Article
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 at 1 institution in 1 country.

Kelly M HastonGladstone Institute of Neurological Disease, San Francisco, California 94158; email: sfinkbeiner@gladstone.ucsf.edu.
Steven FinkbeinerGladstone Institute of Neurological Disease, San Francisco, California 94158; email: sfinkbeiner@gladstone.ucsf.edu.
Gladstone Institutes · US

Funding

Neuron and Glial Cellular Signatures from Normal and Diseased iPS Cells-SupplementU54NS091046 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI FINKBEINER, STEVEN M, FRAENKEL, ERNEST · 2014 to 2020
$11.7M
MECHANISMS OF HUNTINGTIN-INDUCED NEURODEGENERATIONR01NS039074 · NINDS · J. DAVID GLADSTONE INSTITUTES · PI FINKBEINER, STEVEN M · 2000 to 2017
$5.4M
The Huntington's disease (HD) IPS consortiumU24NS078370 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI THOMPSON, LESLIE MICHELS · 2012 to 2013
$2.6M
Automated longitudinal single cell analysisR01NS083390 · NINDS · J. DAVID GLADSTONE INSTITUTES · PI FINKBEINER, STEVEN M · 2013 to 2016
$1.6M
Physical Exam of Human Neurons to Identify Functions of the Druggable GenomeU01MH105035 · NIMH · J. DAVID GLADSTONE INSTITUTES · PI FINKBEINER, STEVEN M · 2014 to 2016
$1.5M
Mechanisms of Neuromuscular Repair by Schwann CellsR01NS045091 · NINDS · DREXEL UNIVERSITY · PI SON, YOUNG-JIN · 2003 to 2006
$992k
NEUROSCIENCE PROGRAMF30MH010501 · NIMH · UNIVERSITY OF ROCHESTER · PI BRENEMAN, STEPHEN M · 1993 to 1997
–
NHGRI NIH HHS U54 HG008105NIMH NIH HHS U01 MH1050135NIMH NIH HHS U01 MH105035NINDS NIH HHS 2 R01 NS045091NINDS NIH HHS 3 R01 NS039074NINDS NIH HHS R01 NS039074NINDS NIH HHS R01 NS045091NINDS NIH HHS R01 NS083390NINDS NIH HHS U24 NS078370NINDS NIH HHS U54 NS091046
6 · The paper itself

Abstract

Neurodegenerative diseases are a leading cause of death. No disease-modifying therapies are available, and preclinical animal model data have routinely failed to translate into success for therapeutics. Induced pluripotent stem cell (iPSC) biology holds great promise for human in vitro disease modeling because these cells can give rise to any cell in the human brain and display phenotypes specific to neurodegenerative diseases previously identified in postmortem and clinical samples. Here, we explore the potential and caveats of iPSC technology as a platform for drug development and screening, and the future potential to use large cohorts of disease-bearing iPSCs to perform clinical trials in a dish.

Indexed as

AnimalsBrainClinical Trials as TopicHumansNeurodegenerative DiseasesPluripotent Stem Cellsclinical trialsdrug developmenthuman pluripotent stem cellsneurodegeneration

Identifiers

PMID26514199
PMCPMC4868344
OpenAlexW1829807625

What OpenQuestion holds

Textmetadata
LicenceTDM
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.