Perturbed Myelination Process of Premyelinating Oligodendrocyte in Niemann-PickType C Mouse

Author:

Takikita Shoichi,Fukuda Takahiro,Mohri Ikuko,Yagi Takashi,Suzuki Kinuko

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

Reference49 articles.

1. Niemann-Pick C1 Disease: Correlations between NPC1 Mutations, Levels of NPC1 Protein, and Phenotypes Emphasize the Functional Significance of the Putative Sterol-Sensing Domain and of the Cysteine-Rich Luminal Loop

2. Niemann-Pick C1 Disease: The I1061T Substitution Is a Frequent Mutant Allele in Patients of Western European Descent and Correlates with a Classic Juvenile Phenotype

3. Genetic heterogeneity in Niemann-Pick C disease: A study using somatic cell hybridization and linkage analysis;Vanier;Am J Hum Genet,1996

4. Niemann-Pick disease type C

5. Higashi Y Murayama S Pentchev P Suzuki K . Pathology of Niemann-Pick type C: Studies of murine mutant. In: Ikuta F , ed. Neuropathology in brain research. Amsterdam: Elsevier, 1991:85–102

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