Evidence map›Paper›PMID 31930086›Full record

ReviewAnnals of translational medicine2019

A compendious summary of Parkinson's disease patient-derived iPSCs in the first decade.

Chao Ren, Fen Wang, Li-Na Guan, Xiao-Yu Cheng, Cai-Yi Zhang, De-Qin Geng, Chun-Feng Liu

Open access · diamondAbstract readReview
In one paragraph

Review in Annals of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 4 institutions in 1 country.

Chao RenDepartment of Neurology, The Second Affiliated Hospital of Soochow University, Suzhou 215004, China.
Fen WangJiangsu Key Laboratory of Neuropsychiatric Diseases and Institute of Neuroscience, Soochow University, Suzhou 215123, China.
Li-Na GuanDepartment of Neurology, The Second Affiliated Hospital of Soochow University, Suzhou 215004, China.
Xiao-Yu ChengDepartment of Neurology, The Second Affiliated Hospital of Soochow University, Suzhou 215004, China.
Cai-Yi ZhangDepartment of Emergency, The Affiliated Hospital of Xuzhou Medical University, Xuzhou 221006, China.
De-Qin GengDepartment of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou 221006, China.
Chun-Feng LiuDepartment of Neurology, The Second Affiliated Hospital of Soochow University, Suzhou 215004, China.
Second Affiliated Hospital of Soochow University · CNSoochow University · CNXuzhou Medical College · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The number of Parkinson's disease (PD) patients increases with aging, which brings heavy burden to families and society. The emergence of patient-derived induced pluripotent stem cells (iPSCs) has brought hope to the current situation of lacking new breakthroughs in diagnosis and treatment of PD. In this article, we reviewed and analyzed the current researches related to PD patient-derived iPSCs, in order to provide solid theoretical basis for future study of PD. In 2008, successful iPSCs derived from PD patients were reported. The current iPSCs research in PD mostly focused on the establishment of specific iPSCs models of PD patients carrying susceptible genes. The main source of PD patient-derived iPSCs is skin fibroblasts and the mainstream reprogramming methodology is the mature "four-factor" method, which introduces four totipotent correlation factors Oct4, Sox2, Klf4 and c-Myc into somatic cells. The main sources of iPSCs are patients with non-pedigrees and there have been no studies involving both PD patients and unaffected carriers within the same family. Most of the existing studies of PD patient-derived iPSCs started with the induction method for obtaining dopaminergic neurons in the first instance, but therapeutic applications are being increased. Although it is not the ultimate panacea, and there are still some unsolved problems (e.g., whether the mutated genes should be corrected or not), a better understanding of iPSCs may be a good gift for both PD patients and doctors due to their advantages in diagnosis and treatment of PD.

Indexed as

cell transplantationdifferentiationdopaminergic neurons (DANs)induced pluripotent stem cells (iPSCs)Parkinson’s disease (PD)

Identifiers

PMID31930086
PMCPMC6944564
OpenAlexW2990654569

What OpenQuestion holds

Textmetadata
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.