(Q44471847)

English

Aspartylglucosaminidase (AGA) is efficiently produced and endocytosed by glial cells: implication for the therapy of a lysosomal storage disorder

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Aspartylglucosaminidase (AGA) is efficiently produced and endocytosed by glial cells: implication for the therapy of a lysosomal storage disorder (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

author name string

Salli Harkke

1

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Minna Laine

2

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Anu Jalanko

3

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

publication date

1 June 2003

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

number of pages

11

1 reference

based on heuristic

inferred from page(s)

Journal of Gene Medicine

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

472-482

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Human leucocyte aspartylglucosaminidase. Evidence for two different subunits in a more complex native structure

1 reference

https://api.crossref.org/works/10.1002%2FJGM.377

21 January 2018

Human aspartylglucosaminidase. A biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblasts

1 reference

https://api.crossref.org/works/10.1002%2FJGM.377

21 January 2018

Neuronal and glial cell type-specific promoters within adenovirus recombinants restrict the expression of the apoptosis-inducing molecule Fas ligand to predetermined brain cell types, and abolish peripheral liver toxicity

1 reference

https://api.crossref.org/works/10.1002%2FJGM.377

21 January 2018

Fibroblast expression of collagens and proteoglycans is altered in aspartylglucosaminuria, a lysosomal storage disease.

1 reference

https://api.crossref.org/works/10.1002%2FJGM.377

21 January 2018

Identifiers

10.1002/JGM.377

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

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