Evidence map›Paper›PMID 34679332›Full record

ArticleBrain sciences2021

Brain Region and Cell Compartment Dependent Regulation of Electron Transport System Components in Huntington's Disease Model Mice.

Johannes Burtscher, Giuseppe Pepe, Federico Marracino, Luca Capocci, Susy Giova, Grégoire P Millet, Alba Di Pardo, Vittorio Maglione

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 89% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 2 institutions in 2 countries.

Johannes BurtscherInstitute of Sport Sciences, University of Lausanne, CH-1015 Lausanne, Switzerland.ORCID 0000-0002-2889-0151
Giuseppe PepeIRCCS Neuromed, 86077 Pozzilli, IS, Italy.
Federico MarracinoIRCCS Neuromed, 86077 Pozzilli, IS, Italy.
Luca CapocciIRCCS Neuromed, 86077 Pozzilli, IS, Italy.
Susy GiovaIRCCS Neuromed, 86077 Pozzilli, IS, Italy.
Grégoire P MilletInstitute of Sport Sciences, University of Lausanne, CH-1015 Lausanne, Switzerland.ORCID 0000-0001-8081-4423
Alba Di PardoIRCCS Neuromed, 86077 Pozzilli, IS, Italy.
Vittorio MaglioneIRCCS Neuromed, 86077 Pozzilli, IS, Italy.
Istituto Neurologico Mediterraneo · ITUniversity of Lausanne · CH

Funding

Fondazione Telethon GGP20101
6 · The paper itself

Abstract

Huntington's disease (HD) is a rare hereditary neurodegenerative disorder characterized by multiple metabolic dysfunctions including defects in mitochondrial homeostasis and functions. Although we have recently reported age-related changes in the respiratory capacities in different brain areas in HD mice, the precise mechanisms of how mitochondria become compromised in HD are still poorly understood. In this study, we investigated mRNA and protein levels of selected subunits of electron transport system (ETS) complexes and ATP-synthase in the cortex and striatum of symptomatic R6/2 mice. Our findings reveal a brain-region-specific differential expression of both nuclear and mitochondrial-encoded ETS components, indicating defects of transcription, translation and/or mitochondrial import of mitochondrial ETS components in R6/2 mouse brains.

Indexed as

cortexHuntington’s diseasemitochondrianeurodegenerationoxidative phosphorylationstriatum

Identifiers

PMID34679332
PMCPMC8533690
OpenAlexW3201687920

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.