Evidence map›Paper›PMID 30898538›Full record

ReviewBiochimica et biophysica acta. Molecular basis of disease2020

Using induced pluripotent stem cell neuronal models to study neurodegenerative diseases.

Xinwen Zhang, Di Hu, Yutong Shang, Xin Qi

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Molecular basis of disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Dopamine Depletion in Parkinson's Disease and Therapeutic Options.CNS & neurological disorders drug targets · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Vesicular Glutamate Release from Feeder-FreehiPSC-Derived Neurons.International journal of molecular sciences · 2022
    Article
  15. Review
  16. Cellular Models for Primary CoQ Deficiency Pathogenesis Study.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Phenotyping Neurodegeneration in Human iPSCs.Annual review of biomedical data science · 2021
    Review
  19. Review
  20. GNeuron · 2020
    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

4 authors.

Xinwen ZhangCenter of Implant Dentistry, School of Stomatology, China Medical University, Shenyang 110002, China; Department of Physiology & Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Di HuDepartment of Physiology & Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Yutong ShangDepartment of Physiology & Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Xin QiDepartment of Physiology & Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA; Center for Mitochondrial Diseases, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA. Electronic address: xxq38@case.edu.

Funding

Role of brain lipid metabolism in Alzheimer's diseaseR01AG065240 · NIA · CASE WESTERN RESERVE UNIVERSITY · PI QI, XIN · 2020 to 2024
$3.0M
Dynamin-related protein 1, neurodegeneration and Huntington's diseaseR01NS088192 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI QI, XIN · 2014 to 2018
$1.7M
Mitochondrial biomarkers in Huntington's diseaseR21NS107897 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI QI, XIN · 2019 to 2019
$453k
NIA NIH HHS R01 AG065240NINDS NIH HHS R01 NS088192NINDS NIH HHS R21 NS107897
6 · The paper itself

Abstract

Current application of human induced pluripotent stem cells (hiPSCs) technology in patient-specific models of neurodegenerative disorders recapitulate some of key phenotypes of diseases, representing disease-specific cellular modeling and providing a unique platform for therapeutics development. We review recent efforts toward advancing hiPSCs-derived neuronal cell types and highlight their potential use for the development of more complex in vitro models of neurodegenerative diseases by focusing on Alzheimer's disease, Parkinson's disease, Huntington's disease and Amyotrophic lateral sclerosis. We present evidence from previous works on the important phenotypic changes of various neuronal types in these neurological diseases. We also summarize efforts on conducting low- and high-throughput screening experiments with hiPSCs toward developing potential therapeutics for treatment of neurodegenerative diseases. Lastly, we discuss the limitations of hiPSCs culture system in studying neurodegenerative diseases and alternative strategies to overcome these hurdles.

Indexed as

Models, NeurologicalAnimalsHumansInduced Pluripotent Stem CellsNeurodegenerative DiseasesDisease modelingInduced pluripotent stem cellsNeurodegenerationNeurodegenerative diseaseNeuronsTherapeutic development

Identifiers

PMID30898538
PMCPMC6751032

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.