JH Wen, XH He, ZS Feng, DY Li, JX Tang… - International Journal of …, 2023 - mdpi.com
The accumulation of protein aggregates is the hallmark of many neurodegenerative diseases. The dysregulation of protein homeostasis (or proteostasis) caused by acute …
K Xu, S Sun, M Yan, J Cui, Y Yang, W Li… - Frontiers in …, 2022 - frontiersin.org
DEAD-box (DDX) 5 and DDX17, which belong to the DEAD-box RNA helicase family, are nuclear and cytoplasmic shuttle proteins. These proteins are expressed in most tissues and …
S Yang, L Winstone, S Mondal, Y Wu - Journal of Biological Chemistry, 2023 - Elsevier
With the development and wide usage of CRISPR technology, the presence of R-loop structures, which consist of an RNA: DNA hybrid and a displaced single strand (ss) DNA …
F Liguori, S Amadio, C Volonté - Cellular and Molecular Life Sciences, 2021 - Springer
Amyotrophic lateral sclerosis (ALS) is a rare, devastating disease, causing movement impairment, respiratory failure and ultimate death. A plethora of genetic, cellular and …
I Martic, F Papaccio, B Bellei, M Cavinato - Frontiers in Physiology, 2023 - frontiersin.org
Aging of human skin is a complex process leading to a decline in homeostasis and regenerative potential of this tissue. Mitochondria are important cell organelles that have a …
M Khan, XXL Chen, M Dias, JR Santos, S Kour… - FEBS …, 2024 - Wiley Online Library
Matrin‐3 (MATR3) is an RNA‐binding protein implicated in neurodegenerative and neurodevelopmental diseases. However, little is known regarding the role of MATR3 in …
S Kour, T Fortuna, EN Anderson, D Mawrie… - Nucleic Acids …, 2023 - academic.oup.com
Mutations in the Fused in Sarcoma (FUS) gene cause the familial and progressive form of amyotrophic lateral sclerosis (ALS). FUS is a nuclear RNA-binding protein involved in RNA …
Y Wang, L Liu, H Chen, Y Yang, C Mu… - Human Molecular …, 2024 - academic.oup.com
Abstract GGGGCC (G4C2) hexanucleotide repeat expansion (HRE) in the first intron of the chromosome 9 open reading frame 72 (C9ORF72) gene is the most common genetic cause …