(Q33737230)

29 July 2017

1 reference

title

The glycosphingolipidoses-from disease to basic principles of metabolism (English)

1 reference

29 July 2017

Schuette CG

1

1 reference

29 July 2017

Doering T

series ordinal

2

1 reference

29 July 2017

Kolter T

series ordinal

3

1 reference

29 July 2017

Sandhoff K

series ordinal

4

1 reference

29 July 2017

1 July 1999

1 reference

29 July 2017

1 reference

29 July 2017

380

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29 July 2017

759-766

1 reference

29 July 2017

7-8

1 reference

AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2

29 July 2017

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Sphingolipid activator proteins are required for epidermal permeability barrier formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Accumulation of protein-bound epidermal glucosylceramides in beta-glucocerebrosidase deficient type 2 Gaucher mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Multivesicular endosomes containing internalized EGF-EGF receptor complexes mature and then fuse directly with lysosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Interaction of the GM2-activator protein with phospholipid-ganglioside bilayer membranes and with monolayers at the air-water interface

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Gaucher's disease: deficiency of 'acid' -glucosidase and reconstitution of enzyme activity in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Effect of bone marrow transplantation on enzyme levels and clinical course in the neurologically affected twitcher mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Collodion babies with Gaucher's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Bone marrow transplantation prolongs life span and ameliorates neurologic manifestations in Sandhoff disease mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Caveolins, a family of scaffolding proteins for organizing "preassembled signaling complexes" at the plasma membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

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/10.1515%2FBC.1999.096

Mice with disrupted GM2/GD2 synthase gene lack complex gangliosides but exhibit only subtle defects in their nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

Lysosomal degradation on vesicular membrane surfaces. Enhanced glucosylceramide degradation by lysosomal anionic lipids and activators.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.1999.096

21 January 2018

Identifiers

DOI

10.1515/BC.1999.096

1 reference

29 July 2017

1 reference