The early phenotype associated with the jimpy mutation of the proteolipid protein gene. [electronic resource]
Producer: 20000424Description: 207-21 p. digitalISSN:- 0300-4864
- Age Factors
- Animals
- Apoptosis
- Astrocytes -- pathology
- Biomarkers
- Cell Count
- Cell Differentiation
- Cells, Cultured
- Demyelinating Diseases -- genetics
- In Situ Hybridization
- Male
- Mice
- Mice, Inbred C3H
- Mice, Jimpy -- genetics
- Microscopy, Electron
- Myelin Proteolipid Protein -- deficiency
- Myelin Sheath -- pathology
- Nerve Tissue Proteins -- analysis
- Oligodendroglia -- pathology
- Phenotype
- Reverse Transcriptase Polymerase Chain Reaction
- Spinal Cord -- pathology
- X Chromosome -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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