(Q73163848)

English

Quantification of mRNAs encoding proteins of the glycosphingolipid catabolism in mouse models of GM2 gangliosidoses and sphingolipid activator protein precursor (prosaposin) deficiency

scientific article published on 01 November 2000

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Quantification of mRNAs encoding proteins of the glycosphingolipid catabolism in mouse models of GM2 gangliosidoses and sphingolipid activator protein precursor (prosaposin) deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference

based on heuristic

inferred from title

encephalopathy due to prosaposin deficiency

1 reference

based on heuristic

inferred from title

Richard L. Proia

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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A Potratz

1

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1 November 2019

S Hüttler

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

U Bierfreund

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

K Suzuki

5

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

K Sandhoff

6

1 reference

Europe PubMed Central

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1 November 2019

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publication date

1 November 2000

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Biochimica et Biophysica Acta

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1502

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

391-397

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Modulation of ganglioside biosynthesis in primary cultured neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The localization of gangliosides in neurons of the central nervous system: the use of anti-ganglioside antibodies

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Topology of glycosphingolipid degradation

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Lysosomal storage diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphi

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Enzyme alterations and lipid storage in three variants of Tay-Sachs disease

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Enzyme-linked Immunosorbent Assay for the Ganglioside GM2-Activator Protein. Screening of Normal Human Tissues and Body Fluids, of Tissues of GM2Gangliosidosis, and for Its Subcellular Localization

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Induced mouse models of abnormal sphingolipid metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Glycosphingolipid degradation and animal models of GM2-gangliosidoses

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel method for real time quantitative RT-PCR.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Real time quantitative PCR

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

GM2 activator protein expression in mouse tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Distribution of saposin proteins (sphingolipid activator proteins) in lysosomal storage and other diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The neuronal ceroid-lipofuscinoses (Batten disease): a new class of lysosomal storage diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Sphingolipid activator proteins (SAPs) are stored together with glycosphingolipids in the infantile neuronal ceroid-lipofuscinosis (INCL)

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900063-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0925-4439(00)00063-6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11068181%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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