Biochemical Characterization of Mutants in Chaperonin Proteins CCT4 and CCT5 Associated with Hereditary Sensory Neuropathy
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference40 articles.
1. Hereditary sensory neuropathy type I;Auer-Grumbach;Orphanet J. Rare Dis,2008
2. Autosomal recessive hereditary sensory neuropathy with spastic paraplegia;Thomas;Brain,1994
3. Hereditary sensory neuropathy with spastic paraplegia;Cavanagh;Brain,1979
4. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation;Rotthier;Brain,2009
5. Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia;Bouhouche;J. Med. Genet,2006
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1. CCT and Cullin1 Regulate the TORC1 Pathway to Promote Dendritic Arborization in Health and Disease;Cells;2024-06-13
2. The role of CCT5 in human tumors: a pan-cancer analysis;2024-06-13
3. CCT and Cullin1 regulate the TORC1 pathway to promote dendritic arborization in health and disease;2023-08-02
4. Histopathology of Skeletal Muscle in a Distal Motor Neuropathy Associated with a Mutant CCT5 Subunit: Clues for Future Developments to Improve Differential Diagnosis and Personalized Therapy;Biology;2023-04-23
5. Structural and Dynamic Disturbances Revealed by Molecular Dynamics Simulations Predict the Impact on Function of CCT5 Chaperonin Mutations Associated with Rare Severe Distal Neuropathies;International Journal of Molecular Sciences;2023-01-19
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