Evidence map›Paper›PMID 24970375›Full record

ArticleScientific reports2014

Ataxia telangiectasia derived iPS cells show preserved x-ray sensitivity and decreased chromosomal instability.

Yoshihiro Fukawatase, Masashi Toyoda, Kohji Okamura, Ken-ichi Nakamura, Kazuhiko Nakabayashi, Shuji Takada, Mayu Yamazaki-Inoue, Akira Masuda, Michiyo Nasu, Kenichiro Hata and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Stem cell models in ataxia-telangiectasia.Neural regeneration research · 2026
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  10. Autonomous trisomic rescue of Down syndrome cells.Laboratory investigation; a journal of technical methods and pathology · 2019
    Article
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  20. Stem cells: the pursuit of genomic stability.International journal of molecular sciences · 2014
    Review
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

14 authors at 4 institutions in 2 countries.

Yoshihiro Fukawatase1] Department of Reproductive Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan [2] School of BioMedical Science, Tokyo Medical and Dental University, Tokyo, 113-0034, Japan.
Masashi Toyoda1] Department of Reproductive Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan [2] Department of Research Team for Geriatric Medicine, Tokyo Metropolitan Institute of Gerontology, Tokyo, 173-0015, Japan.
Kohji OkamuraDepartment of Systems BioMedicine, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.
Ken-ichi NakamuraDepartment of Research Team for Geriatric Pathology, Tokyo Metropolitan Institute of Gerontology, Tokyo, 173-0015, Japan.
Kazuhiko NakabayashiDepartment of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.
Shuji TakadaDepartment of Systems BioMedicine, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.
Mayu Yamazaki-InoueDepartment of Reproductive Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.
Akira MasudaDepartment of Reproductive Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.
Michiyo NasuDepartment of Reproductive Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.
Kenichiro HataDepartment of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.
Kazunori HanaokaDepartment of BioSciences, Kitasato University School of Science, Kanagawa, 252-0373, Japan.
Akon Higuchi1] Department of Chemical and Materials Engineering, National Central University, Taoyuan, 32001, Taiwan [2] College of Science, King Saud University, Riyadh, 11451, Saudi Arabia.
Kaiyo TakuboDepartment of Research Team for Geriatric Pathology, Tokyo Metropolitan Institute of Gerontology, Tokyo, 173-0015, Japan.
Akihiro UmezawaDepartment of Reproductive Biology, National Research Institute for Child Health and Development, Tokyo, 157-8535, Japan.
National Center For Child Health and Development · JPTokyo Metropolitan Institute of Gerontology · JPKitasato University · JPNational Central University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ataxia telangiectasia is a neurodegenerative inherited disease with chromosomal instability and hypersensitivity to ionizing radiation. iPS cells lacking ATM (AT-iPS cells) exhibited hypersensitivity to X-ray irradiation, one of the characteristics of the disease. While parental ataxia telangiectasia cells exhibited significant chromosomal abnormalities, AT-iPS cells did not show any chromosomal instability in vitro for at least 80 passages (560 days). Whole exome analysis also showed a comparable nucleotide substitution rate in AT-iPS cells. Taken together, these data show that ATM is involved in protection from irradiation-induced cell death.

Indexed as

AnimalsApoptosisAtaxia TelangiectasiaAtaxia Telangiectasia Mutated ProteinsBlotting, WesternCell DifferentiationCell ProliferationCells, CulturedCellular ReprogrammingChildChromosomal InstabilityExomeFluorescent Antibody TechniqueHigh-Throughput Nucleotide SequencingHumansImmunoenzyme TechniquesAtaxia Telangiectasia Mutated ProteinsATM protein, humanRNA, Messenger

Identifiers

PMID24970375
PMCPMC4073166
OpenAlexW2019282183

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.