(Q48099707)

8 February 2018

title

Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytes (English)

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8 February 2018

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Alexander Mildner

5

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Hauke Werner

Hauke B Werner

6

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Klaus-Armin Nave

11

Klaus-Armin Nave

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8 February 2018

2

Corinna Lappe-Siefke

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8 February 2018

9

Marco Prinz

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8 February 2018

Britta Brügger

4

Britta Brügger

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8 February 2018

Jens Frahm

10

Jens Frahm

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8 February 2018

author name string

Celia M Kassmann

1

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8 February 2018

Myriam Baes

3

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8 February 2018

Oliver Natt

7

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8 February 2018

Thomas Michaelis

8

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8 February 2018

language of work or name

English

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publication date

22 July 2007

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8 February 2018

published in

Nature Genetics

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8 February 2018

volume

39

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8 February 2018

issue

8

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8 February 2018

page(s)

969-976

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8 February 2018

https://scigraph.springernature.com/pub.10.1038/ng2070

exact match

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cites work

Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy

1 reference

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

21 January 2018

1 reference

Axonal and neuronal degeneration in multiple sclerosis: mechanisms and functional consequences

21 January 2018

1 reference

7 January 2021

Axonal transection in the lesions of multiple sclerosis

1 reference

7 January 2021

Axonal swellings and degeneration in mice lacking the major proteolipid of myelin

1 reference

7 January 2021

Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination

1 reference

7 January 2021

Disease mechanisms in inherited neuropathies

1 reference

7 January 2021

Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia.

1 reference

7 January 2021

Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport

1 reference

7 January 2021

Mammalian peroxisomes and reactive oxygen species

1 reference

7 January 2021

Peroxisomes, lipid metabolism, and peroxisomal disorders

1 reference

7 January 2021

A mouse model for Zellweger syndrome

1 reference

7 January 2021

Oligodendroglial cells in culture effectively dispose of exogenous hydrogen peroxide: comparison with cultured neurones, astroglial and microglial cells.

1 reference

7 January 2021

Opinion: peroxisomal-protein import: is it really that complex?

1 reference

7 January 2021

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

1 reference

7 January 2021

Generation of Pex5-loxP mice allowing the conditional elimination of peroxisomes

1 reference

7 January 2021

High cholesterol level is essential for myelin membrane growth

1 reference

7 January 2021

Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly

1 reference

7 January 2021

Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice

1 reference

7 January 2021

Peroxisomal disorders

1 reference

7 January 2021

Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders

1 reference

7 January 2021

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice

1 reference

7 January 2021

A mouse model for X-linked adrenoleukodystrophy

1 reference

7 January 2021

Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism

1 reference

7 January 2021

Expression of monocyte chemoattractant protein-1 and other beta-chemokines by resident glia and inflammatory cells in multiple sclerosis lesions

1 reference

7 January 2021

MCP-1, MCP-2 and MCP-3 expression in multiple sclerosis lesions: an immunohistochemical and in situ hybridization study

1 reference

7 January 2021

Comparison of myelin, axon, lipid, and immunopathology in the central nervous system of differentially myelin-compromised mutant mice: a morphological and biochemical study

1 reference

7 January 2021

Notch1 control of oligodendrocyte differentiation in the spinal cord

1 reference

7 January 2021

Peroxisomes and oxidative stress

1 reference

7 January 2021

Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantation.

1 reference

7 January 2021

The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder

1 reference

7 January 2021

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

1 reference

7 January 2021

X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment

1 reference

7 January 2021

Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy.

1 reference

7 January 2021

Immunopathogenesis of adrenoleukodystrophy: current understanding

1 reference

7 January 2021

Late onset white matter disease in peroxisome biogenesis disorder

1 reference

7 January 2021

Clinical approach to inherited peroxisomal disorders: a series of 27 patients

1 reference

7 January 2021

The role of CD8(+) T cells in multiple sclerosis and its animal models

1 reference

7 January 2021

Relapsing and remitting multiple sclerosis: pathology of the newly forming lesion

1 reference

7 January 2021

Immune surveillance in the injured nervous system: T-lymphocytes invade the axotomized mouse facial motor nucleus and aggregate around sites of neuronal degeneration.

1 reference

7 January 2021

Immune cells contribute to myelin degeneration and axonopathic changes in mice overexpressing proteolipid protein in oligodendrocytes

1 reference

7 January 2021

High-resolution 3D MRI of mouse brain reveals small cerebral structures in vivo.

1 reference

7 January 2021

Silver Staining of Myelin by Means of Physical Development

1 reference

7 January 2021

Monoclonal antibody O10 defines a conformationally sensitive cell-surface epitope of proteolipid protein (PLP): evidence that PLP misfolding underlies dysmyelination in mutant mice.

1 reference

7 January 2021

Myelination in rat brain: method of myelin isolation.

1 reference

7 January 2021

Interleukin 18-independent engagement of interleukin 18 receptor-alpha is required for autoimmune inflammation

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG2070

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8 February 2018

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8 February 2018