Evidence map›Paper›PMID 33658989›Full record

ArticleFrontiers in immunology2020

A Novel Homozygous Mutation Destabilizes IKKβ and Leads to Human Combined Immunodeficiency.

Tao Qin, Yanjun Jia, Yuhang Liu, Rongxin Dai, Lina Zhou, Satoshi Okada, Miyuki Tsumura, Hidenori Ohnishi, Zenichiro Kato, Hirokazu Kanegane and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Clinical Significance of IKBKB Mutations:Saudi medical journal · 2026
    Review
  2. Article
  3. Article
  4. Case Report: A novelFrontiers in immunology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. 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

12 authors at 7 institutions in 2 countries.

Tao QinDepartment of Infection, Children's Hospital of Chongqing Medical University, Chongqing, China.
Yanjun JiaNational Clinical Research Center for Child Health and Disorders, Chongqing, China.
Yuhang LiuNational Clinical Research Center for Child Health and Disorders, Chongqing, China.
Rongxin DaiNational Clinical Research Center for Child Health and Disorders, Chongqing, China.
Lina ZhouNational Clinical Research Center for Child Health and Disorders, Chongqing, China.
Satoshi OkadaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical & Health Sciences, Hiroshima, Japan.
Miyuki TsumuraDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical & Health Sciences, Hiroshima, Japan.
Hidenori OhnishiDepartment of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
Zenichiro KatoDepartment of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
Hirokazu KaneganeDepartment of Child Health and Development, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Xiulian SunDepartment of Brain Research Institute, Qilu Hospital of Shandong University, Shandong, China.
Xiaodong ZhaoNational Clinical Research Center for Child Health and Disorders, Chongqing, China.
Children's Hospital of Chongqing Medical University · CNChina International Science and Technology Cooperation · CNGifu University · JPHiroshima University · JPChongqing Medical University · CNQilu Hospital of Shandong University · CNTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the

Indexed as

HomozygoteI-kappa B KinaseMutation, MissenseProteolysisSevere Combined ImmunodeficiencySignal TransductionAmino Acid SubstitutionAnimalsFemaleHumansLeukocytes, MononuclearMaleMiceMice, Mutant StrainsI-kappa B KinaseIKBKB protein, humanIkbkb protein, mouseIKKβNF-κBprotein degradationprotein stabilitySCID

Identifiers

PMID33658989
PMCPMC7917045
OpenAlexW3131643348

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.