(Q28592206)

31 January 2017

title

Progression of early postnatal retinal pathology in a mouse model of neuronal ceroid lipofuscinosis (English)

1 reference

CLN8 transmembrane ER and ERGIC protein

31 January 2017

0 references

1 reference

neuronal ceroid lipofuscinosis

GOA release 2020-03-11

1 reference

G. M. Seigel

1

1 reference

31 January 2017

J. Wagner

2

1 reference

31 January 2017

A. Wronska

3

1 reference

31 January 2017

L. Campbell

4

1 reference

31 January 2017

W. Ju

5

1 reference

31 January 2017

N. Zhong

6

1 reference

31 January 2017

publication date

1 December 2005

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31 January 2017

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31 January 2017

volume

19

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31 January 2017

issue

12

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31 January 2017

page(s)

1306–1312

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Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis.

31 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Retinal degeneration in motor neuron degeneration (mnd) mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Retinal pathology and function in a Cln3 knockout mouse model of juvenile Neuronal Ceroid Lipofuscinosis (batten disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Molecular determinants of retinal ganglion cell development, survival, and regeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Optic nerve degeneration in a murine model of juvenile ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Motifs within the CLN3 protein: modulation of cell growth rates and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Pigment variant of neuronal ceroid-lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Vitamin E deficiency and metabolic deficits in neuronal ceroid lipofuscinosis described by bioinformatics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Abnormalities in mitochondria-associated membranes and phospholipid biosynthetic enzymes in the mnd/mnd mouse model of neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

The mitochondrial permeability transition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Mitochondria and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Mitochondrial dysfunction as a cause of optic neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Cell-type-specific opening of the retinal ganglion cell mitochondrial permeability transition pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Oxidative damage and protection of the RPE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

An early-onset congenic strain of the motor neuron degeneration (mnd) mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Northern epilepsy, a new member of the NCL family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Lipofuscin-formation in retinal pigment epithelial cells is reduced by antioxidants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

Apparent loss and hypertrophy of interneurons in a mouse model of neuronal ceroid lipofuscinosis: evidence for partial response to insulin-like growth factor-1 treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

inferred from DOI database lookup

7 January 2021

based on heuristic

Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

inferred from DOI database lookup

7 January 2021

based on heuristic

Mitochondrial damage results in a reversible increase in lysosomal storage material in lymphoblasts from patients with juvenile neuronal ceroid-lipofuscinosis (Batten Disease)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EYE.6701770

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EYE.6701770

1 reference

Dimensions Publication ID

31 January 2017

1000916593

0 references

1 reference