Evidence map›Paper›PMID 38498709›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Mutant huntingtin protein induces MLH1 degradation, DNA hyperexcision, and cGAS-STING-dependent apoptosis.

Xiao Sun, Lu Liu, Chao Wu, Xueying Li, Jinzhen Guo, Junqiu Zhang, Junhong Guan, Nan Wang, Liya Gu, X Willian Yang and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  6. Targeting the cGAS-STING pathway mitigates Huntington disease pathogenesis in a knock-in mouse model.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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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

11 authors at 5 institutions in 2 countries.

Xiao Sun *Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0002-8483-0006
Lu Liu *Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0001-7556-6533
Chao Wu *Department of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0002-8622-4819
Xueying LiDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Jinzhen GuoDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Junqiu ZhangDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0003-1822-8460
Junhong GuanCui-ying Experimental Center, Lanzhou University Second Hospital, Lanzhou 730030, China.ORCID 0000-0003-4900-0610
Nan WangCenter for Neurobehavioral Genetics, Semel Institute for Neuroscience & Human behavior, University of California, Los Angeles, CA 90095.
Liya GuDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390.
X Willian YangCenter for Neurobehavioral Genetics, Semel Institute for Neuroscience & Human behavior, University of California, Los Angeles, CA 90095.
Guo-Min LiDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0002-9842-4578
The University of Texas Southwestern Medical Center · USUniversity of California, Los Angeles · USCapital Medical University · CNLanzhou University Second Hospital · CNWomen's Hospital, School of Medicine, Zhejiang University · CN

Funding

Novel mouse genetic models to study modifiers of Huntington’s diseaseR01NS113612 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI YANG, XIANGDONG WILLIAM · 2019 to 2023
$3.2M
NINDS NIH HHS R01 NS113612
6 · The paper itself

Abstract

Huntington's disease (HD) is an inherited neurodegenerative disorder caused by an expanded CAG repeat in the huntingtin (

Indexed as

Huntington DiseaseApoptosisDNAHumansHuntingtin ProteinMutant ProteinsMutL Protein Homolog 1NucleotidyltransferasesDNAHuntingtin ProteinMLH1 protein, humanMutant ProteinsMutL Protein Homolog 1NucleotidyltransferasescGAS-STINGExo1Huntington’s diseasemHTTMutLα

Identifiers

PMID38498709
PMCPMC10990133
OpenAlexW4392931455

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.