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

title

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

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1 November 2017

Saji M

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1 November 2017

Ukita Y

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1 November 2017

Shinoda Y

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1 November 2017

Taniguchi M

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1 November 2017

Higaki K

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1 November 2017

Ninomiya H

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1 November 2017

Ohno K

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1 November 2017

publication date

1 August 2001

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1 November 2017

published in

Brain and Development

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1 November 2017

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1 November 2017

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1 November 2017

page(s)

288-297

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Recent Advances in Elucidating Niemann‐Pick C Disease

1 November 2017

cites work

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

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

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Murine Model of Niemann-Pick C Disease: Mutation in a Cholesterol Homeostasis Gene

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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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Niemann-Pick disease type C

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

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

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

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

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

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Immunohistochemical expression of P400 protein in Purkinje cells of sphingomyelinosis mouse

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Cerebellar degeneration in the Niemann-Pick type C mouse

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

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

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

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

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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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Astrocytes synthesize apolipoprotein E and metabolize apolipoprotein E-containing lipoproteins

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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

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7 January 2021

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

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7 January 2021

10.1016/S0387-7604(01)00209-1

Identifiers

DOI

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1 November 2017

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