Articles with "cct5" as a keyword



Pan-cancer analysis reveals immunological and prognostic significance of CCT5 in human tumors

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Published in 2025 at "Scientific Reports"

DOI: 10.1038/s41598-025-88339-z

Abstract: The chaperonin containing TCP1 subunit 5 (CCT5) is believed to function as a tumor driver. However, a systematic pan-cancer analysis of CCT5 is still lacking. Therefore, this study aimed to identify the potential role of… read more here.

Keywords: prognostic significance; cancer analysis; analysis; significance cct5 ... See more keywords

Chaperonin-Containing TCP1 Subunit 5 Protects Against the Effect of Mer Receptor Tyrosine Kinase Knockdown in Retinal Pigment Epithelial Cells by Interacting With Filamentous Actin and Activating the LIM-Kinase 1/Cofilin Pathway

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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… read more here.

Keywords: mer receptor; receptor tyrosine; kinase; actin ... See more keywords

Muscle Histopathological Abnormalities in a Patient With a CCT5 Mutation Predicted to Affect the Apical Domain of the Chaperonin Subunit

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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… read more here.

Keywords: apical domain; muscle; subunit; cct5 ... See more keywords

Structural and Dynamic Disturbances Revealed by Molecular Dynamics Simulations Predict the Impact on Function of CCT5 Chaperonin Mutations Associated with Rare Severe Distal Neuropathies

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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… read more here.

Keywords: chaperonin; associated rare; molecular dynamics; cct5 ... See more keywords