Evidence map›Paper›PMID 39456698›Full record

ArticleInternational journal of molecular sciences2024

Role of IL3RA in a Family with Lumbar Spinal Stenosis.

Kai-Ming Liu, Chi-Fan Yang, Weng-Siong H'ng, Hui-Ping Chuang, Eunice Han Xian Khor, Pei-Chun Tsai, Vivia Khosasih, Liang-Suei Lu, Erh-Chan Yeh, Wan-Jia Lin and 4 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kai-Ming LiuNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Chi-Fan YangNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Weng-Siong H'ngNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.ORCID 0000-0002-0571-258X
Hui-Ping ChuangResource Center for Translational Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Eunice Han Xian KhorNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Pei-Chun TsaiNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Vivia KhosasihNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.ORCID 0000-0002-6451-3556
Liang-Suei LuNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Erh-Chan YehNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Wan-Jia LinNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Feng-Jen HsiehNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Chien-Hsiun ChenNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Shiuh-Lin HwangChi Hsien Spine Hospital, Kaohsiung 800, Taiwan.
Jer-Yuarn WuNational Center for Genome Medicine, Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lumbar spinal stenosis (LSS) is a degenerative spinal condition characterized by the narrowing of the spinal canal, resulting in low back pain (LBP) and limited leg mobility. Twin and family studies have suggested that genetics contributes to disease progression. However, the genetic causes of familial LSS remain unclear. We performed whole-exome and direct sequencing on seven female patients from a Han Chinese family with LBP, among whom four developed LSS. Based on our genetic findings, we performed gene knockdown studies in human chondrocytes to study possible pathological mechanisms underlying LSS. We found a novel nonsense mutation, c.417C > G (NM_002183, p.Y139X), in

Indexed as

ChondrocytesLumbar VertebraeSpinal StenosisAdultAgedCollagenFemaleHumansInterleukin-3 Receptor alpha SubunitMaleMatrix Metalloproteinase 1Matrix Metalloproteinase 3Middle AgedPedigreeCollagenIL3RA protein, humanInterleukin-3 Receptor alpha SubunitMatrix Metalloproteinase 1Matrix Metalloproteinase 3collagenestrogen receptorIL3RAIVD degenerationlumbar spinal stenosisMMP

Identifiers

PMID39456698
PMCPMC11507247

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.