Evidence map›Paper›PMID 26443123›Full record

ReviewTrends in molecular medicine2015

Stem and Progenitor Cell-Derived Astroglia Therapies for Neurological Diseases.

Chen Chen, Albert Chan, Han Wen, Seung-Hyuk Chung, Wenbin Deng, Peng Jiang

Open access · greenAbstract readReview
In one paragraph

Review in Trends in molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  5. Therapeutic functions of astrocytes to treat α-synuclein pathology in Parkinson's disease.Proceedings of the National Academy of Sciences of the United States of America · 2022
    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

6 authors at 3 institutions in 1 country.

Chen ChenDepartment of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, CA, USA; Institute for Pediatric Regenerative Medicine, Shriners Hospitals for Children, Sacramento, CA, USA.
Albert ChanDepartment of Pediatrics, University of California, Davis, CA, USA.
Han WenDepartment of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, CA, USA; Institute for Pediatric Regenerative Medicine, Shriners Hospitals for Children, Sacramento, CA, USA.
Seung-Hyuk ChungCollege of Dentistry, University of Illinois, Chicago, IL, USA.
Wenbin DengDepartment of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, CA, USA; Institute for Pediatric Regenerative Medicine, Shriners Hospitals for Children, Sacramento, CA, USA. Electronic address: wbdeng@ucdavis.edu.
Peng JiangDepartment of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, CA, USA; Institute for Pediatric Regenerative Medicine, Shriners Hospitals for Children, Sacramento, CA, USA; Department of Developmental Neuroscience, Munroe-Meyer Institute, University of Nebraska Medical Center, NE, USA. Electronic address: peng.jiang@unmc.edu.
University of California, Davis · USShriners Hospitals for Children - Erie · USUniversity of Illinois Chicago · US

Funding

Differentiation and Integration of Trisomy 21 iPSCs in an Animal ModelR01HD091325 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI TIAN, LIN · 2017 to 2021
$1.6M
Regenerating CNS white matter using induced pluripotent stem cellsR01HD087566 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DENG, WENBIN · 2016 to 2020
$1.5M
Glutamate Receptors in Hypoxic-ischemic Injury to Developing OligodendrocytesR01NS059043 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DENG, WENBIN · 2008 to 2012
$1.4M
NICHD NIH HHS R01 HD087566NICHD NIH HHS R01 HD091325NINDS NIH HHS R01 NS059043
6 · The paper itself

Abstract

Astroglia are a major cellular constituent of the central nervous system (CNS) and play crucial roles in brain development, function, and integrity. Increasing evidence demonstrates that astroglia dysfunction occurs in a variety of neurological disorders ranging from CNS injuries to genetic diseases and chronic degenerative conditions. These new insights herald the concept that transplantation of astroglia could be of therapeutic value in treating the injured or diseased CNS. Recent technological advances in the generation of human astroglia from stem and progenitor cells have been prominent. We propose that a better understanding of the suitability of astroglial cells in transplantation as well as of their therapeutic effects in animal models may lead to the establishment of astroglia-based therapies to treat neurological diseases.

Indexed as

AnimalsAstrocytesCell- and Tissue-Based TherapyCell Culture TechniquesHumansNervous System DiseasesStem Cells

Identifiers

PMID26443123
PMCPMC4637244
OpenAlexW1831595999

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.