Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Myelin: keeping nerves well wrapped up.

Current biology : CB - 1 Jan 1997

Suter U

Abstract excerpt

The recently determined structure of protein zero, P0, the most abundant peripheral nerve myelin protein, provides new insights into the molecular structure of myelin and potential disease mechanisms in hereditary peripheral neuropathies.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Mice
Share to Mutation
Share to Myelin P0 Protein
Share to Myelin Sheath

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Peripheral Nervous System Diseases

Share to Structure-Activity Relationship

Source

Identifiers

PMID: 9072163
DOI: 10.1016/s0960-9822(06)00011-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Myelin: keeping nerves well wrapped up.PMID 9072163Read ↗

How Does Protein Zero Assemble Compact Myelin?Semantic proximity Read ↗

Molecular structure and function of myelin protein P0 in membrane stackingSemantic proximity Read ↗

[Correlation and toxicological significance between myelin protein zero and peripheral nerve disease].Semantic proximity Read ↗

Myelin P0: new knowledge and new roles.Semantic proximity Read ↗

Neuropathy-related mutations alter the membrane binding properties of the human myelin protein P0 cytoplasmic tailSemantic proximity Read ↗

Flexible Players within the Sheaths: The Intrinsically Disordered Proteins of Myelin in Health and DiseaseSemantic proximity Read ↗

Upregulation of large myelin protein zero leads to Charcot-Marie-Tooth disease-like neuropathy in mice.Semantic proximity Read ↗

Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination.Semantic proximity Read ↗

Complete Loss of Myelin protein zero (MPZ) in a patient with a late onset Charcot-Marie-Tooth (CMT).Semantic proximity Read ↗

A nonsense <i>mutation in Myelin Protein Zero</i> causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal functionSemantic proximity Read ↗

Peripheral neuropathies caused by mutations in the myelin protein zero.Semantic proximity Read ↗

Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotypeSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.