Interorganelle communication, aging, and neurodegeneration

M Petkovic, CE O'Brien, YN Jan - Genes & development, 2021 - genesdev.cshlp.org
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 …

Vegetables and their bioactive compounds as anti-aging drugs

H Mechchate, A El Allam, N El Omari, N El Hachlafi… - Molecules, 2022 - mdpi.com
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 …

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 …

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 …

[HTML][HTML] From pathogenesis to therapeutics: a review of 150 years of Huntington's disease research

A Jiang, RR Handley, K Lehnert, RG Snell - International journal of …, 2023 - mdpi.com
Huntington's disease (HD) is a debilitating neurodegenerative genetic disorder caused by
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 …

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 …

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 …

[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 …

MIRRAGGE–minimum information required for reproducible AGGregation experiments

PM Martins, S Navarro, A Silva, MF Pinto… - Frontiers in molecular …, 2020 - frontiersin.org
Reports on phase separation and amyloid formation for multiple proteins and aggregation-
prone peptides are recurrently used to explore the molecular mechanisms associated with …