Mouse model of GM2 activator deficiency manifests cerebellar pathology and motor impairment (Q28504760)

GM2 ganglioside activator protein

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Y. Liu

1

Y

Liu

1 reference

24 January 2017

A. Hoffmann

2

A

Hoffmann

1 reference

24 January 2017

A. Grinberg

3

A

Grinberg

1 reference

24 January 2017

H. Westphal

4

H

Westphal

1 reference

24 January 2017

M. P. McDonald

5

M P

McDonald

1 reference

24 January 2017

K. M. Miller

6

K M

Miller

1 reference

24 January 2017

J. N. Crawley

7

J N

Crawley

1 reference

24 January 2017

K. Sandhoff

8

K

Sandhoff

1 reference

24 January 2017

K. Suzuki

9

K

Suzuki

1 reference

24 January 2017

R. L. Proia

10

R L

Proceedings of the National Academy of Sciences of the United States of America

Proia

1 reference

24 January 2017

language of work or name

English

0 references

publication date

22 July 1997

1 reference

24 January 2017

1 reference

24 January 2017

94

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24 January 2017

15

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24 January 2017

8138–8143

1 reference

24 January 2017

Prevention of lysosomal storage in Tay-Sachs mice treated with N-butyldeoxynojirimycin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

Targeted mutation of the gene encoding the low affinity NGF receptor p75 leads to deficits in the peripheral sensory nervous system

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

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

19 March 2017

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.94.15.8138

Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein.

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

Characterization of full-length cDNAs and the gene coding for the human GM2 activator protein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

Biochemical Basis of Late-Onset Neurolipidoses

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

Quantitative correlation between the residual activity of beta-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21570

Topology of glycosphingolipid degradation.

2 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.94.15.8138

The mouse gene encoding the GM2 activator protein (Gm2a): cDNA sequence, expression, and chromosome mapping.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.94.15.8138

21 January 2018

Identifiers

DOI

10.1073/PNAS.94.15.8138

1 reference

4472561

ADS bibcode

1997PNAS...94.8138L

0 references

4472561

1 reference

1 reference

1 reference