Research progress on the structural and functional roles of hnRNPs in muscle development
Z Li, H Wei, D Hu, X Li, Y Guo, X Ding, H Guo, L Zhang - Biomolecules, 2023 - mdpi.com
Heterogeneous nuclear ribonucleoproteins (hnRNPs) are a superfamily of RNA-binding
proteins consisting of more than 20 members. These proteins play a crucial role in various …
proteins consisting of more than 20 members. These proteins play a crucial role in various …
In neurons, activity-dependent association of dendritically transported mRNA transcripts with the transacting factor CBF-A is mediated by A2RE/RTS elements
CS Raju, N Fukuda, C López-Iglesias… - Molecular biology of …, 2011 - Am Soc Cell Biol
In neurons certain mRNA transcripts are transported to synapses through mechanisms that
are not fully understood. Here we report that the heterogeneous nuclear ribonucleoprotein …
are not fully understood. Here we report that the heterogeneous nuclear ribonucleoprotein …
Autophagy is involved in oligodendroglial precursor-mediated clearance of amyloid peptide
Background Accumulation of β-amyloid peptides is an important hallmark of Alzheimer's
disease (AD). Tremendous efforts have been directed to elucidate the mechanisms of β …
disease (AD). Tremendous efforts have been directed to elucidate the mechanisms of β …
The transacting factor CBF-A/Hnrnpab binds to the A2RE/RTS element of protamine 2 mRNA and contributes to its translational regulation during mouse …
N Fukuda, T Fukuda, J Sinnamon… - PLoS …, 2013 - journals.plos.org
During spermatogenesis, mRNA localization and translation are believed to be regulated in
a stage-specific manner. We report here that the Protamine2 (Prm2) mRNA transits through …
a stage-specific manner. We report here that the Protamine2 (Prm2) mRNA transits through …
Contribution of RNA/DNA binding protein dysfunction in oligodendrocytes in the pathogenesis of the amyotrophic lateral sclerosis/frontotemporal lobar degeneration …
CF Valori, M Neumann - Frontiers in neuroscience, 2021 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are two
incurable neurodegenerative disorders, often considered as the extreme manifestations of a …
incurable neurodegenerative disorders, often considered as the extreme manifestations of a …
MicroRNAs dysregulated in multiple sclerosis affect the differentiation of CG-4 cells, an oligodendrocyte progenitor cell line
O Perdaens, P Bottemanne… - Frontiers in Cellular …, 2024 - frontiersin.org
Introduction Demyelination is one of the hallmarks of multiple sclerosis (MS). While
remyelination occurs during the disease, it is incomplete from the start and strongly …
remyelination occurs during the disease, it is incomplete from the start and strongly …
Dual role of the RNA helicase DDX5 in post-transcriptional regulation of myelin basic protein in oligodendrocytes
P Hoch-Kraft, R White, S Tenzer… - Journal of Cell …, 2018 - journals.biologists.com
In the central nervous system, oligodendroglial expression of myelin basic protein (MBP) is
crucial for the assembly and structure of the myelin sheath. MBP synthesis is tightly …
crucial for the assembly and structure of the myelin sheath. MBP synthesis is tightly …
Transcriptional control of gene expression by actin and myosin
E Louvet, P Percipalle - International review of cell and molecular biology, 2008 - Elsevier
Recent years have witnessed a new turn in the field of gene expression regulation. Actin
and an ever‐growing family of actin‐associated proteins have been accepted as members …
and an ever‐growing family of actin‐associated proteins have been accepted as members …
Sorting mRNA molecules for cytoplasmic transport and localization
N Neriec, P Percipalle - Frontiers in Genetics, 2018 - frontiersin.org
In eukaryotic cells, gene expression is highly regulated at many layers. Nascent RNA
molecules are assembled into ribonucleoprotein complexes that are then released into the …
molecules are assembled into ribonucleoprotein complexes that are then released into the …
Elevated copper remodels hepatic RNA processing machinery in the mouse model of Wilson's disease
Copper is essential to mammalian physiology, and its homeostasis is tightly regulated. In
humans, genetic defects in copper excretion result in copper overload and Wilson's disease …
humans, genetic defects in copper excretion result in copper overload and Wilson's disease …