Overview of myelin, major myelin lipids, and myelin-associated proteins
A Kister, I Kister - Frontiers in Chemistry, 2023 - frontiersin.org
Myelin is a modified cell membrane that forms a multilayer sheath around the axon. It retains
the main characteristics of biological membranes, such as lipid bilayer, but differs from them …
the main characteristics of biological membranes, such as lipid bilayer, but differs from them …
Identification of myelin basic protein proximity interactome using turboid labeling proteomics
EV Smirnova, TV Rakitina, RH Ziganshin, GA Saratov… - Cells, 2023 - mdpi.com
Myelin basic protein (MBP) is one of the key structural elements of the myelin sheath and
has autoantigenic properties in multiple sclerosis (MS). Its intracellular interaction network is …
has autoantigenic properties in multiple sclerosis (MS). Its intracellular interaction network is …
Identification of potential regulatory long non-coding RNA-associated competing endogenous RNA axes in periplaque regions in multiple sclerosis
H Sabaie, S Khorami Rouz, G Kouchakali… - Frontiers in …, 2022 - frontiersin.org
Slow-burning inflammation at the lesion rim is connected to the expansion of chronic
multiple sclerosis (MS) lesions. However, the underlying processes causing expansion are …
multiple sclerosis (MS) lesions. However, the underlying processes causing expansion are …
[HTML][HTML] Myelin basic protein recovery during PKU mice lifespan and the potential role of microRNAs on its regulation
A Bregalda, C Carducci, MT Viscomi, F Pierigè… - Neurobiology of …, 2023 - Elsevier
Untreated phenylketonuria (PKU) patients and PKU animal models show hypomyelination in
the central nervous system and white matter damages, which are accompanied by myelin …
the central nervous system and white matter damages, which are accompanied by myelin …
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 …
Identifying mRNAs Residing in Myelinating Oligodendrocyte Processes as a Basis for Understanding Internode Autonomy
R Gould, S Brady - Life, 2023 - mdpi.com
In elaborating and maintaining myelin sheaths on multiple axons/segments,
oligodendrocytes distribute translation of some proteins, including myelin basic protein …
oligodendrocytes distribute translation of some proteins, including myelin basic protein …
Deconvolution of the MBP-Bri2 Interaction by a Yeast Two Hybrid System and Synergy of the AlphaFold2 and High Ambiguity Driven Protein-Protein Docking
EV Smirnova, TV Rakitina, GA Saratov, AA Kudriaeva… - Crystals, 2022 - mdpi.com
Myelin basic protein (MBP) is one of the key proteins in the development of multiple
sclerosis (MS). However, very few intracellular MBP partners have been identified up to now …
sclerosis (MS). However, very few intracellular MBP partners have been identified up to now …
Myelin Basic Protein Attenuates Furin-Mediated Bri2 Cleavage and Postpones Its Membrane Trafficking
EV Smirnova, VI Timofeev, TV Rakitina… - International Journal of …, 2024 - mdpi.com
Myelin basic protein (MBP) is the second most abundant protein in the central nervous
system and is responsible for structural maintenance of the myelin sheath covering axons …
system and is responsible for structural maintenance of the myelin sheath covering axons …
Myelin basic protein antagonizes the SARS-CoV-2 protein ORF3a-induced autophagy inhibition
GA Saratov, AA Belogurov Jr, AA Kudriaeva - Biochimie, 2024 - Elsevier
Inhibition of autophagy is one of the hallmarks of the SARS-CoV-2 infection. Recently it was
reported that SARS-CoV-2 protein ORF3a inhibits fusion of autophagosomes with …
reported that SARS-CoV-2 protein ORF3a inhibits fusion of autophagosomes with …
Neurodegenerative disorder risk in Krabbe disease carriers
Krabbe disease (KD) is a rare autosomal recessive disorder caused by mutations in the
galactocerebrosidase gene (GALC). Defective GALC causes aberrant metabolism of …
galactocerebrosidase gene (GALC). Defective GALC causes aberrant metabolism of …