The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress (Q24301895)

2

Jeffrey J

Kovacs

1 reference

9 December 2023

Adam McLaurin

3

Adam

McLaurin

1 reference

9 December 2023

Akihiro Ito

5

Akihiro

Ito

1 reference

9 December 2023

Tso Pang Yao

6

Tso Pang

Histone deacetylases: transcriptional repression with SINers and NuRDs

Yao

1 reference

9 December 2023

language of work or name

English

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publication date

12 December 2003

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published in

Cell

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volume

115

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issue

6

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page(s)

727-38

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cites work

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Characterization and dynamics of aggresome formation by a cytosolic GFP-chimera

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Hassles with taking out the garbage: aggravating aggresomes.

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Molecular cloning and characterization of a novel histone deacetylase HDAC10

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Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation

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Histone deacetylase 6 binds polyubiquitin through its zinc finger (PAZ domain) and copurifies with deubiquitinating enzymes

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HDAC6 is a microtubule-associated deacetylase

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Multiple proteolytic systems, including the proteasome, contribute to CFTR processing.

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Aggresomes: a cellular response to misfolded proteins

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Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.

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Cytoplasmic dynein/dynactin mediates the assembly of aggresomes

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ER quality control: the cytoplasmic connection

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Aggresomes, inclusion bodies and protein aggregation

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Inhibition of the ubiquitin-proteasome system in Alzheimer's disease.

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In vivo destabilization of dynamic microtubules by HDAC6-mediated deacetylation

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Retrograde protein translocation: ERADication of secretory proteins in health and disease

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Identification of components of the murine histone deacetylase 6 complex: link between acetylation and ubiquitination signaling pathways

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Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein

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Defective protein folding as a basis of human disease

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Aggregates in neurodegenerative disease: crowds and power?

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Class II histone deacetylases: versatile regulators

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Degradation of CFTR by the ubiquitin-proteasome pathway

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HDAC-6 interacts with and deacetylates tubulin and microtubules in vivo

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The modular nature of histone deacetylase HDAC4 confers phosphorylation-dependent intracellular trafficking.

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