Evidence map›Paper›PMID 33671400›Full record

ArticleGenes2021

De Novo Development of mtDNA Deletion Due to Decreased POLG and SSBP1 Expression in Humans.

Yeonmi Lee, Taeho Kim, Miju Lee, Seongjun So, Mustafa Zafer Karagozlu, Go Hun Seo, In Hee Choi, Peter C W Lee, Chong-Jai Kim, Eunju Kang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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 1 institution in 1 country.

Yeonmi LeeDepartment of Convergence Medicine and Stem Cell Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Taeho KimMedical Genetics Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Miju LeeDepartment of Convergence Medicine and Stem Cell Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Seongjun SoDepartment of Convergence Medicine and Stem Cell Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Mustafa Zafer KaragozluDepartment of Convergence Medicine and Stem Cell Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.ORCID 0000-0002-6749-8654
Go Hun SeoMedical Genetics Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
In Hee ChoiMedical Genetics Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Peter C W LeeDepartment of Biomedical Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.ORCID 0000-0002-2320-6365
Chong-Jai KimDepartment of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Eunju KangDepartment of Convergence Medicine and Stem Cell Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.ORCID 0000-0002-7240-7868
Beom Hee LeeMedical Genetics Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.ORCID 0000-0001-9709-2631
Ulsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defects in the mitochondrial genome (mitochondrial DNA (mtDNA)) are associated with both congenital and acquired disorders in humans. Nuclear-encoded DNA polymerase subunit gamma (

Indexed as

Genetic Predisposition to DiseaseAdolescentAdultChildChild, PreschoolCongenital Bone Marrow Failure SyndromesDNA-Binding ProteinsDNA, MitochondrialDNA Polymerase gammaDNA ReplicationExome SequencingFemaleHumansLipid Metabolism, Inborn ErrorsMaleMitochondrial DiseasesDNA-Binding ProteinsDNA, MitochondrialDNA Polymerase gammaMitochondrial ProteinsNABP2 protein, humanPOLG protein, humanhumanmtDNA deletionPearson syndromePOLGSSBP1

Identifiers

PMID33671400
PMCPMC7922481
OpenAlexW3131870786

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.