(Q28292355)

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

The intracellular transport of low density lipoprotein-derived cholesterol is defective in Niemann-Pick type C fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

A defect in cholesterol esterification in Niemann-Pick disease (type C) patients

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Type-C Niemann-Pick disease: low density lipoprotein uptake is associated with premature cholesterol accumulation in the Golgi complex and excessive cholesterol storage in lysosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Group C Niemann-Pick disease: faulty regulation of low-density lipoprotein uptake and cholesterol storage in cultured fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

The Niemann-Pick C lesion and its relationship to the intracellular distribution and utilization of LDL cholesterol

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Murine Model of Niemann-Pick C Disease: Mutation in a Cholesterol Homeostasis Gene

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Clinical spectrum of Niemann-Pick disease type C.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

A clinical staging classification for type C Niemann-Pick disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097-->T transversion in NPC1.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Intracellular trafficking of cholesterol monitored with a cyclodextrin

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Niemann-Pick type II fibroblasts exhibit impaired cholesterol esterification in response to sphingomyelin hydrolysis

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Translocation of both lysosomal LDL-derived cholesterol and plasma membrane cholesterol to the endoplasmic reticulum for esterification may require common cellular factors involved in cholesterol egress from the acidic compartments (lysosomes/endoso

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

The effect of cholesterol-lowering agents on hepatic and plasma cholesterol in Niemann-Pick disease type C.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Magnetic resonance spectroscopy in Niemann-Pick disease type C: correlation with diagnosis and clinical response to cholestyramine and lovastatin

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Sphingomyelinosis, a new mutation in the mouse: a model of Niemann-Pick disease in humans

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Feline sphingolipidosis resembling Niemann-Pick disease type C

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

A molecular genetic linkage map of mouse chromosome 18, includingspm, Grl-1, Fim-2/c-fms, andMbp

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Niemann-Pick disease type C. Study on the nature of the cerebral storage process

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

GABAergic neuroaxonal dystrophy and other cytopathological alterations in feline Niemann-Pick disease type C

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Pyramidal neurons with ectopic dendrites in storage diseases exhibit increased GM2 ganglioside immunoreactivity

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Accumulation of cholesterol and GM2 ganglioside in cells cultured in the presence of progesterone: an implication for the basic defect in Niemann-Pick disease type C.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Increased levels of GM2 ganglioside in fibroblasts from a patient with juvenile Niemann-Pick disease type C.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Cholesterol reutilization during myelination of regenerating PNS axons is impaired in Niemann-Pick disease type C mice

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Abnormal cholesterol metabolism in imipramine-treated fibroblast cultures. Similarities with Niemann-Pick type C disease

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Type C Niemann-Pick disease: use of hydrophobic amines to study defective cholesterol transport

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

The SREBP pathway: regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021

Complementation studies in Niemann-Pick disease type C indicate the existence of a second group

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901374-4

7 January 2021