Evidence map›Paper›PMID 30030363›Full record

ReviewEssays in biochemistry2018

Mitochondrial transcription and translation: overview.

Aaron R D'Souza, Michal Minczuk

Open access · hybridAbstract readReview
In one paragraph

Review in Essays in biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 162 papers.

0numbers the graph read from it
0cells of the map it votes in
162citing papers in PubMed
10.9field-weighted citation impact, top 1% 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

162 citing papers in PubMed, 295 citations in OpenAlex.

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  19. The complete mitochondrial genome of theMitochondrial DNA. Part B, Resources · 2026
    Article
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102 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Aaron R D'SouzaMRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, U.K.
Michal MinczukMRC Mitochondrial Biology Unit, University of Cambridge, Cambridge, U.K. michal.minczuk@mrc-mbu.cam.ac.uk.
MRC Mitochondrial Biology Unit · GB

Funding

Medical Research Council MC_U105697135Medical Research Council MC_UU_00015/4Medical Research Council MC_UU_00015/7
6 · The paper itself

Abstract

Mitochondria are the major source of ATP in the cell. Five multi-subunit complexes in the inner membrane of the organelle are involved in the oxidative phosphorylation required for ATP production. Thirteen subunits of these complexes are encoded by the mitochondrial genome often referred to as mtDNA. For this reason, the expression of mtDNA is vital for the assembly and functioning of the oxidative phosphorylation complexes. Defects of the mechanisms regulating mtDNA gene expression have been associated with deficiencies in assembly of these complexes, resulting in mitochondrial diseases. Recently, numerous factors involved in these processes have been identified and characterized leading to a deeper understanding of the mechanisms that underlie mitochondrial diseases.

Indexed as

Protein BiosynthesisTranscription, GeneticAdenosine TriphosphateDNA, MitochondrialHumansMitochondriaMitochondrial DiseasesOxidative PhosphorylationRibosomesRNA, MessengerRNA, TransferRNA, Transfer, Amino AcylAdenosine TriphosphateDNA, MitochondrialRNA, MessengerRNA, TransferRNA, Transfer, Amino Acylmitochondriatranslationtrascription

Identifiers

PMID30030363
PMCPMC6056719
OpenAlexW2884073635

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.