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Article

Studies on the effects of altered PMP22 expression during myelination in vitro

1 Apr 1997

Abstract excerpt

Severe inherited dysmyelinating diseases of the peripheral nervous system, the Charcot-Marie-Tooth type1A disease (CMT1A) and the hereditary neuropathy with liability to pressure palsies (HNPP) are associated with a large DNA duplication or deletion of a chromosomal region containing the peripheral myelin protein 22 (PMP22) gene. It has been suggested that a gene dosage effect involving PMP22 is responsible for...

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Identifiers

PMID: 9086179
DOI: 10.1002/(sici)1097-4547(19970401)48:1<31::aid-jnr3>3.0.co;2-f

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Source receipt: pubmed, retrieved 7 Sept 2026.

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Studies on the effects of altered PMP22 expression during myelination in vitroPMID 9086179Read ↗

Identification of the regulatory region of the peripheral myelin protein 22 (PMP22) gene that directs temporal and spatial expression in development and regeneration of peripheral nerves.Semantic proximity Read ↗

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Pmp22 super-enhancer deletion causes tomacula formation and conduction block in peripheral nerves.Semantic proximity Read ↗

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Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

Deletion of the PMP22 gene and hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies.Semantic proximity Read ↗

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