(Q45962890)

18 December 2017

title

A mouse model for the human lysosomal disease aspartylglycosaminuria. (English)

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18 December 2017

author

Vesa Kaartinen

1

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18 December 2017

Nora Heisterkamp

6

object named as

Heisterkamp N

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18 December 2017

author name string

Mononen I

2

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18 December 2017

Voncken JW

3

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18 December 2017

Noronkoski T

4

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18 December 2017

Gonzalez-Gomez I

5

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18 December 2017

Groffen J

7

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18 December 2017

language of work or name

English

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publication date

1 December 1996

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18 December 2017

published in

Nature Medicine

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18 December 2017

volume

2

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18 December 2017

issue

12

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18 December 2017

page(s)

1375-1378

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18 December 2017

Molecular cloning, chromosomal assignment, and expression of the mouse aspartylglucosaminidase gene

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

Gracile axonal dystrophy (GAD), a new neurological mutant in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

Infantile neuroaxonal dystrophy and its relationship to Hallervorden-Spatz disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Derivation of completely cell culture-derived mice from early-passage embryonic stem cells

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Analysis of aspartylglucosamine at the picomole level by high-performance liquid chromatography

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studies

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Aspartylglucosaminuria I: fine structural studies on liver, kidney and brain

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Acid sphingomyelinase-deficient mice mimic the neurovisceral form of human lysosomal storage disease (Niemann-Pick disease)

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Galactosialidosis: neuropathological findings in a case of the late-infantile type

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Recombinant glycosylasparaginase and in vitro correction of aspartylglycosaminuria.

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Correction of deficient enzyme activity in a lysosomal storage disease, aspartylglucosaminuria, by enzyme replacement and retroviral gene transfer

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Assay of aspartylglycosylaminase by high-performance liquid chromatography

1 reference

https://api.crossref.org/works/10.1038%2FNM1296-1375

7 January 2021

Identifiers

DOI

10.1038/NM1296-1375

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18 December 2017

Dimensions Publication ID

1001449695

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1 reference

18 December 2017