Evidence map›Paper›PMID 33911155›Full record

ArticleScientific reports2021

Prenatal transplantation of human amniotic fluid stem cell could improve clinical outcome of type III spinal muscular atrophy in mice.

Steven W Shaw, Shao-Yu Peng, Ching-Chung Liang, Tzu-Yi Lin, Po-Jen Cheng, T'sang-T'ang Hsieh, Hao-Yu Chuang, Paolo De Coppi, Anna L David

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. 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
1.5field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Current Status of Cellular and Gene-Based Therapies for Congenital Metabolic Disorders: A Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Stem Cell-Based Therapeutic Approaches in Genetic Diseases.Advances in experimental medicine and biology · 2023
    Article
  9. Review
  10. Recent research on the treatment of spinal muscular atrophy.Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2022
    Review
  11. Review
  12. 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

9 authors at 7 institutions in 2 countries.

Steven W Shaw *College of Medicine, Chang Gung University, Taoyuan, 333, Taiwan. dr.shaw@me.com.
Shao-Yu Peng *Department of Animal Science, National Pingtung University of Science and Technology, Pingtung, 912, Taiwan.
Ching-Chung LiangDepartment of Obstetrics and Gynecology, Linkou Chang Gung Memorial Hospital, 333, Taoyuan, Taiwan.
Tzu-Yi LinCollege of Medicine, Chang Gung University, Taoyuan, 333, Taiwan.
Po-Jen ChengCollege of Medicine, Chang Gung University, Taoyuan, 333, Taiwan.
T'sang-T'ang HsiehCollege of Medicine, Chang Gung University, Taoyuan, 333, Taiwan.
Hao-Yu ChuangDivision of Neurosurgery, Tainan Municipal An-Nan Hospital, Tainan, 709, Taiwan.
Paolo De CoppiStem Cells and Regenerative Medicine Section, Institute of Child Health, University College London, London, WC1N 1EH, UK.
Anna L DavidPrenatal Cell and Gene Therapy Group, Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, WC1E 6HU, UK.
Chang Gung University · TWLinkou Chang Gung Memorial Hospital · TWAn-Nan Hospital · TWChang Gung Memorial Hospital · TWGreat Ormond Street Hospital · GBNational Pingtung University of Science and Technology · TWUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal muscular atrophy (SMA) is a single gene disorder affecting motor function in uterus. Amniotic fluid is an alternative source of stem cell to ameliorate SMA. Therefore, this study aims to examine the therapeutic potential of Human amniotic fluid stem cell (hAFSC) for SMA. Our SMA model mice were generated by deletion of exon 7 of Smn gene and knock-in of human SMN2. A total of 16 SMA model mice were injected with 1 × 10

Indexed as

AdultAmniotic FluidAnimalsDisease Models, AnimalFemaleHumansMice, TransgenicNeuronsPregnancySpinal Muscular Atrophies of ChildhoodStem CellsStem Cell Transplantation

Identifiers

PMID33911155
PMCPMC8080644
OpenAlexW3158728277

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.