SynthesisPeerJ2025
Systematic review of electron transfer study in DNA relevant to Parkinson's disease and scanning tunneling microscopy.
Synthesis in PeerJ, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Parkinson's disease (PD) is the most typical neurological disorder associated with aging in humans. Since PD has much to do with the medical field, most research studies focus on the biological, chemical, and medical aspects of the investigations, in addition to epidemiological studies, drug intervention studies, and much more. The lack of studies using scanning tunneling microscopy (STM) to investigate the electron transfer properties of DNA in PD opens up a new opportunity to look at electron transfer, which is fundamental to understanding the biological processes of the damage-repair mechanism of DNA in this disease, from a physical perspective. Hence, this systematic review was conducted to identify the methods or techniques currently used in the medical-related fields to study electron transfer in PD. related to electron transfer and PD. Methodology: Scopus, ScienceDirect, and EBSCOhost MEDLINE databases were used to search for literature related to electron transfer and PD. Results: From the thirty studies identified, PD appears to be caused by various causes, including increased levels of cytochrome c, reactive oxygen species produced by the mitochondria, dysfunction of complex I that interferes with the electron transfer process, and mitochondrial dysfunction triggered by PINK1 mutation. 6.7% of prior research has focused on utilizing DNA as a specific sample for investigating electron transfer in synthetic DNA through the use of STM. This highlights a notable lack of research into the potential of DNA in PD, despite the theoretical advantages that STM offers. Conclusions: We propose using STM as a new technique to study electron transfer in the DNA of PD from the physics perspective.
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Registered trials
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.