Neurons in Niemann-Pick disease type C accumulate gangliosides as well as unesterified cholesterol and undergo dendritic and axonal alterations. [electronic resource]
Producer: 20010208Description: 49-64 p. digitalISSN:- 0022-3069
- Animals
- Antigens, CD -- metabolism
- Axons -- pathology
- Cats
- Cerebral Cortex -- metabolism
- Child
- Child, Preschool
- Cholesterol -- metabolism
- Dendrites -- pathology
- Esterification
- Filipin -- metabolism
- G(M2) Ganglioside -- metabolism
- Gangliosides -- metabolism
- Genotype
- Humans
- Intracellular Signaling Peptides and Proteins
- Lysosomal Membrane Proteins
- Membrane Glycoproteins -- metabolism
- Mice
- Mutation
- Neurons -- metabolism
- Niemann-Pick C1 Protein
- Niemann-Pick Diseases -- genetics
- Parvalbumins -- metabolism
- Proteins -- genetics
- Reference Values
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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