Evidence map›Paper›PMID 33435522›Full record

ReviewInternational journal of molecular sciences2021

Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions.

Margherita Protasoni, Massimo Zeviani

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
10.4field-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

126 citing papers in PubMed, 190 citations in OpenAlex.

  1. Review
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  14. Mitochondrial complex I deficiency-associated diseases and models.Cellular and molecular life sciences : CMLS · 2026
    Review
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  20. Article

66 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 2 institutions in 2 countries.

Margherita ProtasoniMitochondrial Biology Unit, The MRC and University of Cambridge, Cambridge CB2 0XY, UK.
Massimo ZevianiMitochondrial Biology Unit, The MRC and University of Cambridge, Cambridge CB2 0XY, UK.
University of Cambridge · GBUniversity of Padua · IT

Funding

European Research Council FP7-322424Fondazione Telethon GGP19007Medical Research Council MC_UU_00015/5
6 · The paper itself

Abstract

Mitochondria are ubiquitous intracellular organelles found in almost all eukaryotes and involved in various aspects of cellular life, with a primary role in energy production. The interest in this organelle has grown stronger with the discovery of their link to various pathologies, including cancer, aging and neurodegenerative diseases. Indeed, dysfunctional mitochondria cannot provide the required energy to tissues with a high-energy demand, such as heart, brain and muscles, leading to a large spectrum of clinical phenotypes. Mitochondrial defects are at the origin of a group of clinically heterogeneous pathologies, called mitochondrial diseases, with an incidence of 1 in 5000 live births. Primary mitochondrial diseases are associated with genetic mutations both in nuclear and mitochondrial DNA (mtDNA), affecting genes involved in every aspect of the organelle function. As a consequence, it is difficult to find a common cause for mitochondrial diseases and, subsequently, to offer a precise clinical definition of the pathology. Moreover, the complexity of this condition makes it challenging to identify possible therapies or drug targets.

Indexed as

MutationAnimalsDNA, MitochondrialEnergy MetabolismHumansMitochondriaMitochondrial DiseasesMitochondrial ProteinsModels, MolecularProtein ConformationDNA, MitochondrialMitochondrial ProteinsATP productionbiogenesis of the respiratory chainmitochondrial diseasemi-tochondrial electrochemical gradientmitochondrial potentialmitochondrial proton pumpingmitochondrial respiratory chainoxidative phosphorylationrespiratory complexrespiratory supercomplex

Identifiers

PMID33435522
PMCPMC7827222
OpenAlexW3119310506

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.