Results 21 to 30 of about 228,458 (257)

The Human Myelin Proteome and Sub-Metalloproteome Interaction Map: Relevance to Myelin-Related Neurological Diseases

open access: yesBrain Sciences, 2022
Myelin in humans is composed of about 80% lipids and 20% protein. Initially, myelin protein composition was considered low, but various recent proteome analyses have identified additional myelin proteins.
Christos T. Chasapis   +4 more
doaj   +1 more source

Confined Multilamellae Prefer Cylindrical Morphology [PDF]

open access: yes, 2005
By evaporating a drop of lipid dispersion we generate the myelin morphology often seen in dissolving surfactant powders. We explain these puzzling nonequilibrium structures using a geometric argument: The bilayer repeat spacing increases and thus the ...
Huang, Jung-Ren   +2 more
core   +1 more source

Focus on 1,25-Dihydroxyvitamin D3 in the Peripheral Nervous System

open access: yesFrontiers in Neuroscience, 2019
In this review, we draw attention to the roles of calcitriol (1,25-dihydroxyvitamin D3) in the trophicity of the peripheral nervous system. Calcitriol has long been known to be crucial in phosphocalcium homeostasis. However, recent discoveries concerning
Pierre Antoine Faye   +11 more
doaj   +1 more source

Towards in vivo g-ratio mapping using MRI: unifying myelin and diffusion imaging [PDF]

open access: yes, 2020
The g-ratio, quantifying the comparative thickness of the myelin sheath encasing an axon, is a geometrical invariant that has high functional relevance because of its importance in determining neuronal conduction velocity.
Callaghan, Martina F.   +1 more
core   +3 more sources

RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant

open access: yesOrphanet Journal of Rare Diseases, 2019
Background Ribonucleases (RNases) are crucial for degradation of ribosomal RNA (rRNA). RNASET2 as a subtype of RNASEs is a 256 amino acid protein, encoded by RNASET2 gene located on chromosome six.
Reyhaneh Kameli   +9 more
doaj   +1 more source

Learning Myelin Content in Multiple Sclerosis from Multimodal MRI through Adversarial Training [PDF]

open access: yes, 2018
Multiple sclerosis (MS) is a demyelinating disease of the central nervous system (CNS). A reliable measure of the tissue myelin content is therefore essential for the understanding of the physiopathology of MS, tracking progression and assessing ...
Ayache, Nicholas   +6 more
core   +3 more sources

Myelin pathology: Involvement of molecular chaperones and the promise of chaperonotherapy [PDF]

open access: yes, 2019
The process of axon myelination involves various proteins including molecular chaperones. Myelin alteration is a common feature in neurological diseases due to structural and functional abnormalities of one or more myelin proteins.
Cappello F.   +4 more
core   +1 more source

Disruption of Sema3A/Plexin‐A1 inhibitory signalling in oligodendrocytes as a therapeutic strategy to promote remyelination

open access: yesEMBO Molecular Medicine, 2019
Current treatments in multiple sclerosis (MS) are modulating the inflammatory component of the disease, but no drugs are currently available to repair lesions.
Fabien Binamé   +12 more
doaj   +1 more source

MicroRNA-23a promotes myelination in the central nervous system. [PDF]

open access: yes, 2013
Demyelinating disorders including leukodystrophies are devastating conditions that are still in need of better understanding, and both oligodendrocyte differentiation and myelin synthesis pathways are potential avenues for developing treatment ...
Fu, Ying-Hui   +5 more
core   +2 more sources

Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation

open access: yesClinical Case Reports, 2021
We report a patient with complex clinical presentation including multiple neurological symptoms and eye involvement. Upon genetic investigation, the patient was found to carry a novel homozygous mutation in the NDUFS4 gene, thus adding to the ...
Mohammad Vafaee‐Shahi   +6 more
doaj   +1 more source

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