Evidence map›Paper›PMID 29661920›Full record

ArticleMolecular and cellular biology2018

DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice.

Wang-Yang Xu, Houbao Zhu, Yan Shen, Ying-Han Wan, Xiao-Die Tu, Wen-Ting Wu, Lingyun Tang, Hong-Xin Zhang, Shun-Yuan Lu, Xiao-Long Jin and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Junctions in Jeopardy: the neuromuscular junction is a selective pathological target in Charcot-Marie-Tooth disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
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  15. HeterozygousGenes · 2021
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  18. Knock-Out ofFrontiers in endocrinology · 2021
    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

12 authors at 2 institutions in 1 country.

Wang-Yang Xu *State Key Laboratory of Medical Genomics, Research Center for Experimental Medicine of Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Houbao Zhu *State Key Laboratory of Medical Genomics, Research Center for Experimental Medicine of Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.ORCID 0000-0002-7553-1557
Yan ShenState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine of Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ying-Han WanShanghai Research Center for Model Organisms, Shanghai, China.
Xiao-Die TuShanghai Research Center for Model Organisms, Shanghai, China.
Wen-Ting WuShanghai Research Center for Model Organisms, Shanghai, China.
Lingyun TangState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine of Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Hong-Xin ZhangState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine of Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shun-Yuan LuState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine of Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Xiao-Long JinDepartment of Pathology, Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Jian FeiShanghai Research Center for Model Organisms, Shanghai, China.
Zhu-Gang WangState Key Laboratory of Medical Genomics, Research Center for Experimental Medicine of Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China zhugangw@shsmu.edu.cn.
Shanghai Jiao Tong University · CNShanghai Model Organisms (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DHTKD1, a part of 2-ketoadipic acid dehydrogenase complex, is involved in lysine and tryptophan catabolism. Mutations in

Indexed as

2-Aminoadipic AcidAdipatesAnimalsCharcot-Marie-Tooth DiseaseCodon, NonsenseDisease Models, AnimalEarly Growth Response Protein 2HumansInsulinKetoglutarate Dehydrogenase ComplexKetone OxidoreductasesMaleMetabolic Networks and PathwaysMiceMice, Inbred C57BLMice, Knockout2-Aminoadipic AcidAdipatesCodon, NonsenseDHTKD1 protein, humanEarly Growth Response Protein 2Egr2 protein, mouseInsulinKetoglutarate Dehydrogenase ComplexKetone OxidoreductasesMpz protein, mouseMyelin P0 Protein2-aminoadipic acid2-aminoadipic and 2-oxoadipic aciduriaCharcot-Marie-Tooth diseaseDHTKD1nerve conduction velocity

Identifiers

PMID29661920
PMCPMC6002691
OpenAlexW2797220239

What OpenQuestion holds

Textmetadata
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.