Impaired Intracellular Trafficking Is a Common Disease Mechanism ofPMP22Point Mutations in Peripheral Neuropathies
- 28 February 1999
- journal article
- Published by Elsevier in Neurobiology of Disease
- Vol. 6 (1) , 1-14
- https://doi.org/10.1006/nbdi.1998.0227
Abstract
No abstract availableKeywords
This publication has 70 references indexed in Scilit:
- Analysis of compound heterozygous mice reveals that theTrembler mutation can behave as a gain-of-function alleleJournal of Neuroscience Research, 1997
- Ins and outs of peripheral myelin protein-22: Mapping transmembrane topology and intracellular sortingJournal of Neuroscience Research, 1997
- HNMP-1: A Novel Hematopoietic and Neural Membrane Protein Differentially Regulated in Neural Development and InjuryJournal of Neuroscience, 1997
- Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32Journal of Neuroscience, 1997
- Heterozygous Peripheral Myelin Protein 22-Deficient Mice Are Affected by a Progressive Demyelinating Tomaculous NeuropathyJournal of Neuroscience, 1997
- Studies on the effects of altered PMP22 expression during myelination in vitroJournal of Neuroscience Research, 1997
- Widespread expression of the peripheral myelin protein‐22 gene (pmp22) in neural and non‐neural tissues during murine developmentJournal of Neuroscience Research, 1995
- Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient miceNature Genetics, 1995
- DNA deletion associated with hereditary neuropathy with liability to pressure palsiesCell, 1993
- Studies on cultured rat Schwann cells. I. Establishment of purified populations from cultures of peripheral nerveBrain Research, 1979