Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations (Q36559669)

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scientific article published on 17 January 2008

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English	Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations	scientific article published on 17 January 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

protein ubiquitination

1 reference

based on heuristic

inferred from title

Infantile neuroaxonal dystrophy

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based on heuristic

inferred from title

author name string

Ibrahim Malik

1

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

John Turk

2

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Europe PubMed Central

PMC publication ID

14 August 2017

David J Mancuso

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Laura Montier

4

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Mary Wohltmann

5

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

David F Wozniak

6

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Robert E Schmidt

7

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Richard W Gross

8

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Paul T Kotzbauer

9

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Europe PubMed Central

PMC publication ID

14 August 2017

language of work or name

0 references

publication date

17 January 2008

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Europe PubMed Central

PMC publication ID

14 August 2017

The American Journal of Pathology

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Europe PubMed Central

PMC publication ID

14 August 2017

172

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Europe PubMed Central

PMC publication ID

14 August 2017

2

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Europe PubMed Central

PMC publication ID

14 August 2017

406-416

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PLA2G6 mutation underlies infantile neuroaxonal dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Insulin secretory responses and phospholipid composition of pancreatic islets from mice that do not express Group VIA phospholipase A2 and effects of metabolic stress on glucose homeostasis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Highly selective hydrolysis of fatty acyl-CoAs by calcium-independent phospholipase A2beta. Enzyme autoacylation and acyl-CoA-mediated reversal of calmodulin inhibition of phospholipase A2 activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Differential regulation of EGF receptor internalization and degradation by multiubiquitination within the kinase domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Spontaneous murine neuroaxonal dystrophy: a model of infantile neuroaxonal dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Altered neuronal mitochondrial coenzyme A synthesis in neurodegeneration with brain iron accumulation caused by abnormal processing, stability, and catalytic activity of mutant pantothenate kinase 2

1 reference

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30 September 2017

Lysosomal targeting of E-cadherin: a unique mechanism for the down-regulation of cell-cell adhesion during epithelial to mesenchymal transitions

1 reference

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30 September 2017

Neurodegenerative diseases: a decade of discoveries paves the way for therapeutic breakthroughs

1 reference

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30 September 2017

Male mice that do not express group VIA phospholipase A2 produce spermatozoa with impaired motility and have greatly reduced fertility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Misfolding diverts CFTR from recycling to degradation: quality control at early endosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Neuropathology and pathogenesis of diabetic autonomic neuropathy

1 reference

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30 September 2017

Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Neuropathology of gracile axonal dystrophy (GAD) mouse. An animal model of central distal axonopathy in primary sensory neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Neuroaxonal dystrophy in aging human sympathetic ganglia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Genetic and age related models of neurodegeneration in mice: dystrophic axons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

30 September 2017

Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and lewy body pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Widespread occurrence of alpha-synuclein/NACP-immunoreactive neuronal inclusions in juvenile and adult-onset Hallervorden-Spatz disease with Lewy bodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Amyloid beta precursor protein and ubiquitin epitopes in human and experimental dystrophic axons. Ultrastructural localization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Neuroaxonal dystrophy in young adults: a clinicopathological study of two unrelated cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

An analysis of the ultrastructural findings in infantile neuroaxonal dystrophy (Seitelberger's disease).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Infantile neuroaxonal dystrophy. Histological and electron microscopical study of two cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Histological and ultrastructural features of dystrophic isocortical axons in infantile neuroaxonal dystrophy (Seitelberger's disease).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Terminal axon pathology in infantile neuroaxonal dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Infantile neuroaxonal dystrophy (Seitelberger's disease). A light and ultrastructural study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

28 June 2018

Cerebellar synaptic defects and abnormal motor behavior in mice lacking alpha- and beta-dystrobrevin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

21 September 2018

Apoptotic neurodegeneration induced by ethanol in neonatal mice is associated with profound learning/memory deficits in juveniles followed by progressive functional recovery in adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

21 September 2018

Fibrillization of alpha-synuclein and tau in familial Parkinson's disease caused by the A53T alpha-synuclein mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

21 September 2018

Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

21 September 2018

Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

21 September 2018

Alpha-synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2312364

21 October 2018

Involvement of group VI Ca2+-independent phospholipase A2 in protein kinase C-dependent arachidonic acid liberation in zymosan-stimulated macrophage-like P388D1 cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18202189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Both proteasomes and lysosomes degrade the activated erythropoietin receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/18202189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/18202189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neuroaxonal dystrophy. Early form with preferential cerebellar involvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/18202189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neuroaxonal dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18202189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha-synuclein immunoreactivity is present in axonal swellings in neuroaxonal dystrophy and acute traumatic brain injury

1 reference

https://pubmed.ncbi.nlm.nih.gov/18202189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.2353/AJPATH.2008.070823

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

ResearchGate publication ID

0 references

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