Evidence map›Paper›PMID 25103020›Full record

ReviewMolecular biology reports2014

Mitochondrial dynamic changes in health and genetic diseases.

Le Chen, Allison J Winger, Anne A Knowlton

Abstract readReview
In one paragraph

Review in Molecular biology reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
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  7. Review
  8. Review
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  13. Review
  14. Article
  15. Mitochondrial transplantation for therapeutic use.Clinical and translational medicine · 2016
    Review
  16. Article
  17. Mitochondrial Fission Factor Gene Mutation: A Dilemma for Prenatal Diagnosis.International journal of applied & basic medical research
    Article
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

3 authors.

Le ChenMolecular & Cellular Cardiology, University of California, Davis, One Shields Avenue Davis, CA, 95616, USA, lechen@ucdavis.edu.
Allison J Winger
Anne A Knowlton

Funding

Human Cardiomyopathy and HSP60R01HL077281 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI KNOWLTON, ANNE A · 2004 to 2012
$3.1M
HSPs, Inflammatory Response and Cardiovascular DiseaseR01HL079071 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KNOWLTON, ANNE A · 2006 to 2014
$2.7M
NHLBI NIH HHS HL077281NHLBI NIH HHS HL079071NHLBI NIH HHS R01 HL077281NHLBI NIH HHS R01 HL079071
6 · The paper itself

Abstract

Mitochondria are highly specialized in function, but mitochondrial and, therefore, cellular integrity is maintained through their dynamic nature. Through the frequent processes of fusion and fission, mitochondria continuously change in shape and adjust function to meet cellular requirements. Abnormalities in fusion/fission dynamics generate cellular dysfunction that may lead to diseases. Mutations in the genes encoding mitochondrial fusion/fission proteins, such as MFN2 and OPA1, have been associated with an increasing number of genetic disorders, including Charcot-Marie-Tooth disease type 2A (CMT2A) and autosomal dominant optic atrophy. In this review, we address the mitochondrial dynamic changes in several important genetic diseases, which will bring the new insight of clinical relevance of mitochondrial genetics.

Indexed as

ApoptosisGenetic Diseases, InbornGTP PhosphohydrolasesHumansMitochondrial DiseasesMitochondrial DynamicsMitochondrial ProteinsOxidative StressGTP PhosphohydrolasesMFN2 protein, humanMitochondrial ProteinsOPA1 protein, human

Identifiers

PMID25103020
PMCPMC5683169

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Registered trials

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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.