Autophagy-lysosome pathway associated neuropathology and axonal degeneration in the brains of alpha-galactosidase A-deficient mice (Q37600470)

21 August 2017

Autophagy-lysosome pathway associated neuropathology and axonal degeneration in the brains of alpha-galactosidase A-deficient mice (English)

1 reference

21 August 2017

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5

Edgar A Jaimes

1 reference

21 August 2017

Michael P Nelson

1

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21 August 2017

Tonia E Tse

2

1 reference

21 August 2017

Darrel B O'Quinn

3

1 reference

21 August 2017

Stefanie M Percival

4

1 reference

21 August 2017

David G Warnock

6

1 reference

21 August 2017

John J Shacka

7

1 reference

21 August 2017

14 February 2014

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Acta Neuropathologica Communications

21 August 2017

1 reference

21 August 2017

2

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20

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describes a project that uses

21 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3933238/fullTextXML

inferred from PubMed Central ID database lookup

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23 August 2017

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23 August 2017

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Stroke in Fabry disease frequently occurs before diagnosis and in the absence of other clinical events: natural history data from the Fabry Registry

23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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Cathepsin D is the main lysosomal enzyme involved in the degradation of alpha-synuclein and generation of its carboxy-terminally truncated species

23 August 2017

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Immunohistologic techniques for detecting the glycolipid Gb(3) in the mouse kidney and nervous system

23 August 2017

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Sphingolipid metabolism diseases

23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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23 August 2017

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LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing

23 August 2017

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alpha-Galactosidase A deficient mice: a model of Fabry disease

23 August 2017

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Cerebrovascular complications of Fabry's disease

23 August 2017

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Mouse models of neuronal ceroid lipofuscinoses: useful pre-clinical tools to delineate disease pathophysiology and validate therapeutics

23 August 2017

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6 September 2017

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Neuronopathic Gaucher disease in the mouse: viable combined selective saposin C deficiency and mutant glucocerebrosidase (V394L) mice with glucosylsphingosine and glucosylceramide accumulation and progressive neurological deficits

6 September 2017

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Acid β-glucosidase mutants linked to Gaucher disease, Parkinson disease, and Lewy body dementia alter α-synuclein processing.

6 September 2017

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Lysosomal enzyme cathepsin D protects against alpha-synuclein aggregation and toxicity

14 September 2017

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Toxicity of glucosylsphingosine (glucopsychosine) to cultured neuronal cells: a model system for assessing neuronal damage in Gaucher disease type 2 and 3.

14 September 2017

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Correction of enzymatic and lysosomal storage defects in Fabry mice by adenovirus-mediated gene transfer

14 September 2017

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Autophagosome maturation is impaired in Fabry disease

28 September 2017

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Wild type alpha-synuclein is degraded by chaperone-mediated autophagy and macroautophagy in neuronal cells

25 June 2018

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Anderson-Fabry's disease: neuropathological and neurochemical investigation.

25 June 2018

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Neuroaxonal regeneration is more pronounced in early multiple sclerosis than in traumatic brain injury lesions.

25 June 2018

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Lysosomal dysfunction in a mouse model of Sandhoff disease leads to accumulation of ganglioside-bound amyloid-β peptide

1 September 2018

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Genetic analysis of lysosomal alpha-galactosidase A gene in sporadic Parkinson's disease

1 September 2018

1 reference

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Decreased expression of lysosomal alpha-galactosiase A gene in sporadic Parkinson's disease.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933238

The MAP1-LC3 conjugation system is involved in lipid droplet formation

1 September 2018

1 reference

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Neurophysiological, behavioral and morphological abnormalities in the Fabry knockout mice.

1 September 2018

1 reference

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Cellular and tissue localization of globotriaosylceramide in Fabry disease.

1 September 2018

1 reference

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Cathepsin D deficiency induces persistent neurodegeneration in the absence of Bax-dependent apoptosis.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933238

Parkinsonism and Anderson Fabry's disease: a case report.

1 September 2018

1 reference

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Alpha-synuclein phosphorylation controls neurotoxicity and inclusion formation in a Drosophila model of Parkinson disease

1 September 2018

1 reference

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Clearance of alpha-synuclein oligomeric intermediates via the lysosomal degradation pathway.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933238

White matter lesions in Fabry disease occur in 'prior' selectively hypometabolic and hyperperfused brain regions

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933238

Ubiquitination of alpha-synuclein in Lewy bodies is a pathological event not associated with impairment of proteasome function

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933238

Fabry disease in mice is associated with age-dependent susceptibility to vascular thrombosis

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933238

Phosphorylated alpha-synuclein is ubiquitinated in alpha-synucleinopathy lesions

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3933238

Kidney histologic alterations in α-Galactosidase-deficient mice

1 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186/2051-5960-2-20

Enzymatic Defect in Fabry's Disease

21 January 2018

1 reference

12 December 2020

A histochemical and electron microscopic study of skeletal and cardiac muscle from a Fabry disease patient and carrier

1 reference

12 December 2020

Decreased activities of lysosomal acid alpha-D-galactosidase A in the leukocytes of sporadic Parkinson's disease

1 reference

12 December 2020

1 reference

12 December 2020

Brain MRI findings in patients with Fabry disease

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12 December 2020

Identifiers

DOI

10.1186/2051-5960-2-20

1 reference

Dimensions Publication ID

21 August 2017

0 references

1 reference

21 August 2017

PubMed publication ID

24529306

1 reference