(Q38464244)

3 September 2017

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title

Neuroaxonal dystrophy in PLA2G6 knockout mice (English)

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3 September 2017

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neuroaxonal dystrophy

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Hisae Sumi-Akamaru

1

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3 September 2017

Goichi Beck

series ordinal

2

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3 September 2017

Shinsuke Kato

series ordinal

3

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3 September 2017

Hideki Mochizuki

series ordinal

4

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3 September 2017

publication date

6 May 2015

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3 September 2017

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3 September 2017

volume

35

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3 September 2017

issue

3

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3 September 2017

page(s)

289-302

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Diversity and function of membrane glycerophospholipids generated by the remodeling pathway in mammalian cells

3 September 2017

cites work

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https://api.crossref.org/works/10.1111%2FNEUP.12202

Lipidomic analysis and electron transport chain activities in C57BL/6J mouse brain mitochondria

21 January 2018

1 reference

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Recent progress in phospholipase A₂ research: from cells to animals to humans

21 January 2018

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Neuronal phospholipid deacylation is essential for axonal and synaptic integrity

21 January 2018

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Generation of membrane diversity by lysophospholipid acyltransferases

21 January 2018

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https://api.crossref.org/works/10.1111%2FNEUP.12202

Distribution of calcium-independent phospholipase A2 (iPLA 2) in monkey brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Calcium-independent phospholipase A2 localizes in and protects mitochondria during apoptotic induction by staurosporine

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

PLA2G6 mutation underlies infantile neuroaxonal dystrophy

21 January 2018

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https://api.crossref.org/works/10.1111%2FNEUP.12202

Characterization of PLA2G6 as a locus for dystonia-parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism

21 January 2018

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Neurodegeneration associated with genetic defects in phospholipase A(2).

21 January 2018

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PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort

21 January 2018

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New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations

21 January 2018

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Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: implications for molecular diagnosis.

21 January 2018

1 reference

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Infantile neuroaxonal dystrophy. A disease characterized by altered terminal axons and synaptic endings.

21 January 2018

1 reference

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

21 January 2018

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https://api.crossref.org/works/10.1111%2FNEUP.12202

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

21 January 2018

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Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations

21 January 2018

1 reference

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Extensive aggregation of α-synuclein and tau in juvenile-onset neuroaxonal dystrophy: an autopsied individual with a novel mutation in the PLA2G6 gene-splicing site

21 January 2018

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https://api.crossref.org/works/10.1111%2FNEUP.12202

Neuroaxonal dystrophy caused by group VIA phospholipase A2 deficiency in mice: a model of human neurodegenerative disease.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Genetic ablation of PLA2G6 in mice leads to cerebellar atrophy characterized by Purkinje cell loss and glial cell activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Establishment of an improved mouse model for infantile neuroaxonal dystrophy that shows early disease onset and bears a point mutation in Pla2g6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Catalytic function of PLA2G6 is impaired by mutations associated with infantile neuroaxonal dystrophy but not dystonia-parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Peripheral nerve biopsy as an aid to diagnosis in infantile neuroaxonal dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Formation of 4-hydroxynonenal from cardiolipin oxidation: Intramolecular peroxyl radical addition and decomposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

iPLA2β knockout mouse, a genetic model for progressive human motor disorders, develops age-related neuropathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

The emerging role of group VI calcium-independent phospholipase A2 in releasing docosahexaenoic acid from brain phospholipids

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Functional role of cardiolipin in mitochondrial bioenergetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

Disturbed brain phospholipid and docosahexaenoic acid metabolism in calcium-independent phospholipase A(2)-VIA (iPLA(2)β)-knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FNEUP.12202

21 January 2018

Identifiers

DOI

10.1111/NEUP.12202

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3 September 2017

1 reference