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Published in 2022 at "Frontiers in Medicine"
DOI: 10.3389/fmed.2022.861371
Abstract: Retinitis pigmentosa (RP), characterized by the gradual loss of rod and cone photoreceptors that eventually leads to blindness, is the most common inherited retinal disorder, affecting more than 2.5 million people worldwide. However, the underlying…
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Keywords:
mer receptor;
receptor tyrosine;
kinase;
actin ... See more keywords
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Published in 2022 at "Frontiers in Molecular Biosciences"
DOI: 10.3389/fmolb.2022.887336
Abstract: Recognition of diseases associated with mutations of the chaperone system genes, e.g., chaperonopathies, is on the rise. Hereditary and clinical aspects are established, but the impact of the mutation on the chaperone molecule and the…
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Keywords:
apical domain;
muscle;
subunit;
cct5 ... See more keywords
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Published in 2023 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms24032018
Abstract: Mutations in genes encoding molecular chaperones, for instance the genes encoding the subunits of the chaperonin CCT (chaperonin containing TCP-1, also known as TRiC), are associated with rare neurodegenerative disorders. Using a classical molecular dynamics…
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Keywords:
chaperonin;
associated rare;
molecular dynamics;
cct5 ... See more keywords