(Q33536410)

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Pathogenesis of inclusion bodies in (CAG)n/Qn-expansion diseases with special reference to the role of tissue transglutaminase and to selective vulnerability

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Europe PubMed Central

PubMed publication ID

27 July 2017

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Europe PubMed Central

Pathogenesis of inclusion bodies in (CAG)n/Qn-expansion diseases with special reference to the role of tissue transglutaminase and to selective vulnerability (English)

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Europe PubMed Central

PubMed publication ID

27 July 2017

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author name string

Cooper AJ

1

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Sheu KF

2

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Europe PubMed Central

PubMed publication ID

27 July 2017

Burke JR

3

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Strittmatter WJ

4

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Gentile V

5

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Peluso G

6

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Europe PubMed Central

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27 July 2017

Blass JP

7

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Europe PubMed Central

PubMed publication ID

27 July 2017

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publication date

1 March 1999

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Europe PubMed Central

PubMed publication ID

27 July 2017

Journal of Neurochemistry

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Europe PubMed Central

PubMed publication ID

27 July 2017

72

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Europe PubMed Central

PubMed publication ID

27 July 2017

3

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Europe PubMed Central

PubMed publication ID

27 July 2017

889-899

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Spinobulbar muscular atrophy: polyglutamine-expanded androgen receptor is proteolytically resistant in vitro and processed abnormally in transfected cells.

1 reference

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Immunohistochemical detection of coagulation factor XIIIa in postmortem human brain tissue.

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The association of tissue transglutaminase with human recombinant tau results in the formation of insoluble filamentous structures.

1 reference

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21 January 2018

Core histones are glutaminyl substrates for tissue transglutaminase

1 reference

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21 January 2018

Transgenic models of Huntington's disease

1 reference

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21 January 2018

Aging, energy, and oxidative stress in neurodegenerative diseases.

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Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length

1 reference

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21 January 2018

Trinucleotide repeat length and clinical progression in Huntington's disease

1 reference

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21 January 2018

Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia.

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Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.

1 reference

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21 January 2018

Comparative studies on tissue transglutaminase and factor XIII

1 reference

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21 January 2018

Transglutaminase-catalyzed inactivation of glyceraldehyde 3-phosphate dehydrogenase and alpha-ketoglutarate dehydrogenase complex by polyglutamine domains of pathological length

1 reference

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21 January 2018

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

1 reference

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21 January 2018

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

1 reference

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21 January 2018

Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Transglutaminase facilitates the formation of polymers of the beta-amyloid peptide

1 reference

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21 January 2018

Expression of tissue transglutaminase in Balb-C 3T3 fibroblasts: effects on cellular morphology and adhesion

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Tissue transglutaminase-catalyzed formation of high-molecular-weight aggregates in vitro is favored with long polyglutamine domains: a possible mechanism contributing to CAG-triplet diseases.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract

1 reference

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21 January 2018

Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset

1 reference

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21 January 2018

Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Spinocerebellar ataxia type 6: CAG repeat expansion in α1a voltage‐dependent calcium channel gene and clinical variations in japanese population

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Identification of amine acceptor protein substrates of transglutaminase in liver extracts: use of 5-(biotinamido) pentylamine as a probe

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

The cortical neuritic pathology of Huntington's disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Transglutaminase activity is increased in Alzheimer's disease brain

1 reference

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21 January 2018

Peptides containing glutamine repeats as substrates for transglutaminase-catalyzed cross-linking: relevance to diseases of the nervous system

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Transglutaminase action imitates Huntington's disease: selective polymerization of Huntingtin containing expanded polyglutamine.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Transglutaminase aggregates huntingtin into nonamyloidogenic polymers, and its enzymatic activity increases in Huntington's disease brain nuclei

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Huntingtin immunoreactivity in the rat neostriatum: differential accumulation in projection and interneurons

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

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Huntingtin-associated protein (HAP1): discrete neuronal localizations in the brain resemble those of neuronal nitric oxide synthase

1 reference

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21 January 2018

Neurodegenerative diseases and transglutaminase

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

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Polyglutamines, nuclear inclusions and neurodegeneration

1 reference

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Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

1 reference

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Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

1 reference

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The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1

1 reference

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Toxicity of expanded polyglutamine-domain proteins in Escherichia coli.

1 reference

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Ectopically Expressed CAG Repeats Cause Intranuclear Inclusions and a Progressive Late Onset Neurological Phenotype in the Mouse

1 reference

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A role for transglutaminase in neurotransmitter release by rat brain synaptosomes

1 reference

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21 January 2018

Trinucleotide repeats in neurogenetic disorders

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Machado-Joseph disease gene product is a cytoplasmic protein widely expressed in brain

1 reference

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Glutamine repeats and inherited neurodegenerative diseases: molecular aspects

1 reference

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Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases

1 reference

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gamma-Glutamylaminotransferase and transglutaminase in subcellular fractions of rat cortex and in cultured astrocytes

1 reference

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21 January 2018

Intranuclear neuronal inclusions: a common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?

1 reference

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Huntington's Disease and Dentatorubral‐Pallidoluysian Atrophy: Proteins, Pathogenesis and Pathology

1 reference

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21 January 2018

Evidence for a preferential loss of enkephalin immunoreactivity in the external globus pallidus in low grade Huntington's disease using high resolution image analysis

1 reference

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21 January 2018

Huntingtin localization in brains of normal and Huntington's disease patients

1 reference

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Identification of an HD patient with a (CAG)180 repeat expansion and the propagation of highly expanded CAG repeats in lambda phage

1 reference

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21 January 2018

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

1 reference

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Association of putrescine, spermidine, spermine, and GABA with structural elements of brain cells

1 reference

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Alzheimer's Disease: Insolubility of Partially Purified Paired Helical Filaments in Sodium Dodecyl Sulfate and Urea

1 reference

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Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

1 reference

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Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Incorporation of glutamine repeats makes protein oligomerize: implications for neurodegenerative diseases

1 reference

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21 January 2018

Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

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Chemical synthesis of the gene for microbial transglutaminase from Streptoverticillium and its expression in Escherichia coli.

1 reference

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21 January 2018

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

1 reference

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Huntington's disease gene product, huntingtin, associates with microtubules in vitro

1 reference

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21 January 2018

Toward understanding the molecular pathology of Huntington's disease.

1 reference

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21 January 2018

Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Modulation of the in situ activity of tissue transglutaminase by calcium and GTP.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Pharmacologic inhibition of transglutaminase-induced cross-linking of Alzheimer's amyloid beta-peptide

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720889.X

21 January 2018

Inhibition of α-ketoglutarate-and pyruvate dehydrogenase complexes in E. coli by a glutathione S-transferase containing a pathological length poly-Q domain: A possible role of energy deficit in neurological diseases associated with poly-Q expansions

1 reference

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21 January 2018

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10.1046/J.1471-4159.1999.0720889.X

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

ResearchGate publication ID

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