Evidence map›Paper›PMID 36646944›Full record

ArticleJournal of human genetics2023

Intellectual disability and abnormal cortical neuron phenotypes in patients with Bloom syndrome.

Hideo Kaneko, Chizuru Kawase, Junko Seki, Yasuhiro Ikawa, Akihiro Yachie, Michinori Funato

Abstract read
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In one paragraph

Article in Journal of human genetics, 2023. 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
0.6field-weighted citation impact, top 26% 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, 2 citations in OpenAlex.

  1. Review
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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.

Hideo KanekoDepartment of Pediatric Medical Care, Gifu Prefectural General Medical Center, Gifu, Japan. kaneko-hideo@gifu-hp.jp.ORCID http://orcid.org/0000-0002-9269-8017
Chizuru KawaseDepartment of Clinical Research, National Hospital Organization, Nagara Medical Center, Gifu, Japan.
Junko SekiDepartment of Clinical Research, National Hospital Organization, Nagara Medical Center, Gifu, Japan.
Yasuhiro IkawaDepartment of Pediatrics, School of Medicine Institute of Medical Pharmaceutical and Health Science, Kanazawa University, Kanazawa, Japan.
Akihiro YachieDivision of Medical Safety, Kanazawa University Hospital, Kanazawa, Japan.
Michinori FunatoDepartment of Clinical Research, National Hospital Organization, Nagara Medical Center, Gifu, Japan.
Nagara Medical Center · JPKanazawa University · JPKanazawa University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bloom syndrome (BS) is a rare autosomal recessive disorder characterized by genomic instability that leads to various complications, including cancer. Given the low prevalence of BS in Japan, we conducted a nationwide survey. We recruited eight patients with BS, three of whom exhibited intellectual disability. The 631delCAA mutation in the BLM gene was detected in 9 out of 16 alleles. To investigate neuronal development in patients with BS, we generated induced pluripotent stem cells derived from one of these patients (BS-iPSCs). We examined the phenotypes of the induced cortical neurons derived from the generated BS-iPSCs using a previously reported protocol; the generated BS-iPSCs showed an approximately 10-times higher frequency of sister-chromatid exchange (SCE) than the control iPSCs. Immunocytochemistry revealed shorter axons and higher proliferative potential in BS-iPSC-derived cortical neurons compared with control iPSCs. To our knowledge, our study is the first to clarify the abnormality of the cortical neuron phenotypes derived from patients with BS. Our findings may help identify the pathogenesis of neuronal differentiation in BS and aid in the development of novel therapeutic agents.

Indexed as

Bloom SyndromeIntellectual DisabilityHumansMutationNeuronsPhenotype

Identifiers

PMID36646944
OpenAlexW4316653568

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.