Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein. [electronic resource]
Producer: 20060323Description: 3469-77 p. digitalISSN:- 1529-2401
- Animals
- Animals, Newborn
- Arginine -- genetics
- Blotting, Western -- methods
- Brain -- metabolism
- Cells, Cultured
- Cerebellum -- cytology
- Cricetinae
- Cricetulus
- Detergents -- pharmacology
- Disease Models, Animal
- Electrophoresis, Polyacrylamide Gel -- methods
- Fluorescent Antibody Technique -- methods
- Gene Expression
- Glial Fibrillary Acidic Protein -- metabolism
- Golgi Apparatus -- metabolism
- Golgi Matrix Proteins
- Immunoprecipitation -- methods
- Leucine -- genetics
- Membrane Proteins -- metabolism
- Methionine -- pharmacokinetics
- Mice
- Mice, Inbred C57BL
- Mice, Transgenic
- Mutation
- Neurodegenerative Diseases -- genetics
- Neurons
- Octoxynol -- pharmacology
- PrPSc Proteins -- genetics
- Prion Diseases -- genetics
- Protein Structure, Tertiary -- genetics
- RNA, Messenger -- metabolism
- Reverse Transcriptase Polymerase Chain Reaction -- methods
- Sulfur Isotopes -- pharmacokinetics
- Time Factors
- Type C Phospholipases -- pharmacology
- Valine -- genetics
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Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
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