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Interorganelle communication, aging, and neurodegeneration
Our cells are comprised of billions of proteins, lipids, and other small molecules packed into
their respective subcellular organelles, with the daunting task of maintaining cellular …
their respective subcellular organelles, with the daunting task of maintaining cellular …
Vegetables and their bioactive compounds as anti-aging drugs
Aging is a continuous process over time that is mainly related to natural alterations in
mechanical–biological processes. This phenomenon is due to several factors, including the …
mechanical–biological processes. This phenomenon is due to several factors, including the …
Tau and neurofilament light‐chain as fluid biomarkers in spinocerebellar ataxia type 3
H Garcia‐Moreno, M Prudencio… - European journal of …, 2022 - Wiley Online Library
Background and purpose Clinical trials in spinocerebellar ataxia type 3 (SCA3) will require
biomarkers for use as outcome measures. Methods To evaluate total tau (t‐tau), glial …
biomarkers for use as outcome measures. Methods To evaluate total tau (t‐tau), glial …
Voltage-Gated Ca2+-Channel α1-Subunit de novo Missense Mutations: Gain or Loss of Function – Implications for Potential Therapies
J Striessnig - Frontiers in synaptic neuroscience, 2021 - frontiersin.org
This review summarizes our current knowledge of human disease-relevant genetic variants
within the family of voltage gated Ca2+ channels. Ca2+ channelopathies cover a wide …
within the family of voltage gated Ca2+ channels. Ca2+ channelopathies cover a wide …
[HTML][HTML] From pathogenesis to therapeutics: a review of 150 years of Huntington's disease research
Huntington's disease (HD) is a debilitating neurodegenerative genetic disorder caused by
an expanded polyglutamine-coding (CAG) trinucleotide repeat in the huntingtin (HTT) gene …
an expanded polyglutamine-coding (CAG) trinucleotide repeat in the huntingtin (HTT) gene …
Abnormal mitochondrial quality control in neurodegenerative diseases
X Yan, B Wang, Y Hu, S Wang, X Zhang - Frontiers in Cellular …, 2020 - frontiersin.org
Neurodegenerative diseases, including Alzheimer's, Parkinson's, Huntington's, and
amyotrophic lateral sclerosis, are characterized by a progressive loss of selective neuron …
amyotrophic lateral sclerosis, are characterized by a progressive loss of selective neuron …
Neuroprotective effects of a small mitochondrially-targeted tetrapeptide elamipretide in neurodegeneration
NT Nhu, SY **ao, Y Liu, VB Kumar, ZY Cui… - Frontiers in Integrative …, 2022 - frontiersin.org
Neural mitochondrial dysfunction, neural oxidative stress, chronic neuroinflammation, toxic
protein accumulation, and neural apoptosis are common causes of neurodegeneration …
protein accumulation, and neural apoptosis are common causes of neurodegeneration …
NAADP-Evoked Ca2+ Signaling Leads to Mutant Huntingtin Aggregation and Autophagy Impairment in Murine Astrocytes
CAS Pereira, NC Medaglia, RP Ureshino… - International journal of …, 2023 - mdpi.com
Huntington's disease (HD) is a progressive neurodegenerative disease characterized by
mutations in the huntingtin gene (mHtt), causing an unstable repeat of the CAG trinucleotide …
mutations in the huntingtin gene (mHtt), causing an unstable repeat of the CAG trinucleotide …
[HTML][HTML] Mutant-huntingtin molecular pathways elucidate new targets for drug repurposing
VS Makeeva, NS Dyrkheeva, OI Lavrik… - International Journal of …, 2023 - mdpi.com
The spectrum of neurodegenerative diseases known today is quite extensive. The
complexities of their research and treatment lie not only in their diversity. Even many years of …
complexities of their research and treatment lie not only in their diversity. Even many years of …
MIRRAGGE–minimum information required for reproducible AGGregation experiments
Reports on phase separation and amyloid formation for multiple proteins and aggregation-
prone peptides are recurrently used to explore the molecular mechanisms associated with …
prone peptides are recurrently used to explore the molecular mechanisms associated with …