NeuralCipher Open access
Genetic Sketch of Parkinson's Disease in India.
DOI: 10.4103/aian.aian_1021_24PMID: 40335451
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15.097 articles found
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Parishin C modulates the amyloid transformation of alpha-synuclein protein by apparently interacting with the NAC domain.
DOI: 10.1016/j.bbapap.2025.141076PMID: 40345607
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Neural and vascular contributions to sensory impairments in a human alpha-synuclein transgenic mouse model of Parkinson's disease.
DOI: 10.1177/0271678x251338952PMID: 40334688
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Ligands for Protein Fibrils of Amyloid-β, α-Synuclein, and Tau.
DOI: 10.1021/acs.chemrev.4c00838PMID: 40327808
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PQK7: A novel peptide inhibitor targeting alpha-synuclein fibrillogenesis in Parkinson's disease.
DOI: 10.1016/j.npep.2025.102522PMID: 40339505
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Tailored pharmacotherapy monitoring in Parkinson's disease and Schizophrenia using a rapid and sensitive α-Synuclein assay.
DOI: 10.1016/j.cca.2025.120349PMID: 40339684
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Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebellar Disorders.
DOI: 10.1002/mds.30210PMID: 40326640
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The most common structural variant expected at the <i>GBA1</i> locus may be detected by a simple amplification method: Implications for screening Parkinson's disease variants.
DOI: 10.1016/j.prdoa.2025.100338PMID: 40470483
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Plain Language Summary Publication: Investigating the causal and genetic relationship between migraine and Parkinson's disease.
DOI: 10.1111/head.14947PMID: 40320910
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Effect of hydrogen sulfide on alpha-synuclein aggregation and cell viability.
DOI: 10.1038/s41598-025-99794-zPMID: 40320462
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Investigating shared genetic architecture between pigmentation genetics and Parkinson’s Disease
DOI: 10.1101/2025.04.30.25326753
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Emergent glutamate & dopamine dysfunction in VPS35<sub>(D620N)</sub> knock-in mice and rapid reversal by LRRK2 inhibition.
DOI: 10.1038/s41531-025-00948-7PMID: 40319043
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