(Q28299661)

1

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B C Lewis

2

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J F Edwards

3

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J Alroy

4

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B J Zeng

5

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P A Torres

6

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K N Bretzlaff

Glycosphingolipid disorders of the brain

7

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language of work or name

English

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publication date

July 2011

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published in

Veterinary Pathology

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volume

48

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issue

4

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page(s)

807-13

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cites work

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Neurodegenerative lysosomal storage disease in European Burmese cats with hexosaminidase beta-subunit deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Effective gene therapy in an authentic model of Tay-Sachs-related diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

GM 2 Ganglioside Lysosomal Storage Disease in Cats with α-Hexosaminidase Deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

GM2 gangliosidosis in a Japanese spaniel

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Abnormalities of developing white matter in lysosomal storage diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Naturally occurring GM2 gangliosidosis in two Muntjak deer with pathological and biochemical features of human classical Tay-Sachs disease (type B GM2 gangliosidosis).

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Morphology of the Gangliosidoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Apoptotic cell death in mouse models of GM2 gangliosidosis and observations on human Tay-Sachs and Sandhoff diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Glycosphingolipid lysosomal storage diseases: therapy and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Central nervous system inflammation is a hallmark of pathogenesis in mouse models of GM1 and GM2 gangliosidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Mechanism of abnormal growth in astrocytes derived from a mouse model of GM2 gangliosidosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Mutation of the GM2 activator protein in a feline model of GM2 gangliosidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Characterization of a new model of GM2-gangliosidosis (Sandhoff's disease) in Korat cats

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Inhibition of calcium uptake via the sarco/endoplasmic reticulum Ca2+-ATPase in a mouse model of Sandhoff disease and prevention by treatment with N-butyldeoxynojirimycin

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Distortion of neuronal geometry and formation of aberrant synapses in neuronal storage disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Functions of sphingolipid metabolism in mammals--lessons from genetic defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Neuropathology of mice with targeted disruption of Hexa gene, a model of Tay-Sachs disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

The leukoencephalopathy of infantile GM1 gangliosidosis: oligodendrocytic loss and axonal dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Secondary accumulation of gangliosides in lysosomal storage disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Gangliosides as modulators of dendritogenesis in normal and storage disease-affected pyramidal neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Sphingosine kinase 1/S1P receptor signaling axis controls glial proliferation in mice with Sandhoff disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Deletion of macrophage-inflammatory protein 1 alpha retards neurodegeneration in Sandhoff disease mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

Spontaneous appearance of Tay-Sachs disease in an animal model

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985810388522

21 January 2018

Identifiers

DOI

10.1177/0300985810388522

1 reference

Consolidated OpenCitations Corpus – April 2017

release_io2d4q2zhbfafhd77h6632qgha

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/io2d4q2zhbfafhd77h6632qgha

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

21123862

1 reference

Consolidated OpenCitations Corpus – April 2017