Progressive neuronal loss in the ventral posterior lateral and medial nuclei of thalamus in Niemann-Pick disease type C mouse brain (Q42508615)

1 November 2017

Progressive neuronal loss in the ventral posterior lateral and medial nuclei of thalamus in Niemann-Pick disease type C mouse brain (English)

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Niemann-Pick disease, type C1

1 November 2017

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Yamada A

1

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1 November 2017

Saji M

2

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1 November 2017

Ukita Y

3

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1 November 2017

Shinoda Y

4

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1 November 2017

Taniguchi M

5

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1 November 2017

Higaki K

6

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1 November 2017

Ninomiya H

7

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1 November 2017

Ohno K

8

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1 November 2017

1 August 2001

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1 November 2017

Brain and Development

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1 November 2017

23

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1 November 2017

5

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1 November 2017

288-297

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Recent advances in elucidating Niemann-Pick C disease

1 November 2017

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Sphingomyelinosis, a new mutation in the mouse: a model of Niemann-Pick disease in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

A mouse model for Niemann-Pick disease. Influence of genetic background on disease expression in spm/spm mice

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene.

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

A C57BL/KsJ mouse model of Niemann-Pick disease (spm) belongs to the same complementation group as the major childhood type of Niemann-Pick disease type C.

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Niemann-Pick disease type C

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

The Niemann-Pick C1 protein resides in a vesicular compartment linked to retrograde transport of multiple lysosomal cargo

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Maternal Pumilio acts together with Nanos in germline development in Drosophila embryos

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Role of Niemann-Pick type C1 protein in intracellular trafficking of low density lipoprotein-derived cholesterol.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Cerebellar involvement in murine sphingomyelinosis: a new model of Niemann-Pick disease

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Decreased membrane fluidity and unsaturated fatty acids in Niemann-Pick disease type C fibroblasts

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Immunohistochemical expression of P400 protein in Purkinje cells of sphingomyelinosis mouse

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Cerebellar degeneration in the Niemann-Pick type C mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Niemann-Pick disease type C. Study on the nature of the cerebral storage process.

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Neurofibrillary tangles in Niemann-Pick disease type C.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Neurological manifestations of Niemann-Pick disease type C in cats.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

GABAergic neuroaxonal dystrophy and other cytopathological alterations in feline Niemann-Pick disease type C.

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Clinical spectrum of Niemann-Pick disease type C.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Niemann-Pick disease. Morphologic and biochemical studies in the visceral form with late central nervous system involvement (Crocker's group C).

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

A case of juvenile lipidosis: electron microscopic, histochemical and biochemical studies

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Biochemical studies in Niemann-Pick disease. I. Major sphingolipids of liver and spleen

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Cholesterol and oxygenated cholesterol concentrations are markedly elevated in peripheral tissue but not in brain from mice with the Niemann-Pick type C phenotype.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Alleviation of neuronal ganglioside storage does not improve the clinical course of the Niemann-Pick C disease mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Cholesterol is sequestered in the brains of mice with Niemann-Pick type C disease but turnover is increased.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Astrocytes synthesize apolipoprotein E and metabolize apolipoprotein E-containing lipoproteins

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Cholesterol accumulation in tissues of the Niemann-pick type C mouse is determined by the rate of lipoprotein-cholesterol uptake through the coated-pit pathway in each organ

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

Embryonic Striatal Neurons from Niemann-Pick Type C Mice Exhibit Defects in Cholesterol Metabolism and Neurotrophin Responsiveness

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900209-1

7 January 2021

10.1016/S0387-7604(01)00209-1

Identifiers

DOI

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1 November 2017

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