Proteome profile of myelin in the zebrafish brain
SB Siems, O Jahn, LJ Hoodless, RB Jung… - Frontiers in cell and …, 2021 - frontiersin.org
The velocity of nerve conduction along vertebrate axons depends on their ensheathment
with myelin. Myelin membranes comprise specialized proteins well characterized in mice …
with myelin. Myelin membranes comprise specialized proteins well characterized in mice …
Structural and functional evolution of 2′, 3′-cyclic nucleotide 3′-phosphodiesterase
M Myllykoski, L Seidel, G Muruganandam, A Raasakka… - Brain research, 2016 - Elsevier
Abstract 2′, 3′-cyclic nucleotide 3′-phosphodiesterase (CNPase) is an abundant
membrane-associated enzyme within the vertebrate myelin sheath. While the physiological …
membrane-associated enzyme within the vertebrate myelin sheath. While the physiological …
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules
S Tikka, E Monogioudi, A Gotsopoulos… - Neuromolecular …, 2016 - Springer
Neuronal ceroid lipofuscinoses (NCL) are the most commonly inherited progressive
encephalopathies of childhood. Pathologically, they are characterized by endolysosomal …
encephalopathies of childhood. Pathologically, they are characterized by endolysosomal …
CNP blocks mitochondrial depolarization and inhibits SARS-CoV-2 replication in vitro and in vivo
J Logue, VM Melville, J Ardanuy, MB Frieman - PLoS pathogens, 2023 - journals.plos.org
The COVID-19 pandemic has claimed over 6.5 million lives worldwide and continues to
have lasting impacts on the world's healthcare and economic systems. Several approved …
have lasting impacts on the world's healthcare and economic systems. Several approved …
Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking
Protein zero (P0) is the major structural component of peripheral myelin. Lack of this
adhesion protein from Schwann cells causes a severe dysmyelinating neuropathy with …
adhesion protein from Schwann cells causes a severe dysmyelinating neuropathy with …
Investigating brain connectivity heritability in a twin study using diffusion imaging data
Heritability of brain anatomical connectivity has been studied with diffusion-weighted
imaging (DWI) mainly by modeling each voxel's diffusion pattern as a tensor (eg, to compute …
imaging (DWI) mainly by modeling each voxel's diffusion pattern as a tensor (eg, to compute …
Proteomics‐level analysis of myelin formation and regeneration in a mouse model for vanishing white matter disease
I Gat‐Viks, T Geiger, M Barbi, G Raini… - Journal of …, 2015 - Wiley Online Library
Vanishing white matter (VWM) is a recessive neurodegenerative disease caused by
mutations in translation initiation factor eIF 2B and leading to progressive brain myelin …
mutations in translation initiation factor eIF 2B and leading to progressive brain myelin …
Determinants of ligand binding and catalytic activity in the myelin enzyme 2′, 3′-cyclic nucleotide 3′-phosphodiesterase
A Raasakka, M Myllykoski, S Laulumaa, M Lehtimäki… - Scientific Reports, 2015 - nature.com
Abstract 2′, 3′-cyclic nucleotide 3′-phosphodiesterase (CNPase) is an enzyme highly
abundant in the central nervous system myelin of terrestrial vertebrates. The catalytic …
abundant in the central nervous system myelin of terrestrial vertebrates. The catalytic …
Biomedical applications of ion mobility-enhanced data-independent acquisition-based label-free quantitative proteomics
Mass spectrometry-based proteomics greatly benefited from recent improvements in
instrument performance and the development of bioinformatics solutions facilitating the high …
instrument performance and the development of bioinformatics solutions facilitating the high …
Decreased turnover of the CNS myelin protein Opalin in a mouse model of hereditary spastic paraplegia 35
Abstract Spastic paraplegia 35 (SPG35)(OMIM: 612319) or fatty acid hydroxylase-
associated neurodegeneration (FAHN) is caused by deficiency of fatty acid 2-hydroxylase …
associated neurodegeneration (FAHN) is caused by deficiency of fatty acid 2-hydroxylase …