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

Mitochondrial dynamics and inherited peripheral nerve diseases.

Neuroscience letters - 2 Jun 2015

Pareyson Davide, Saveri Paola, Sagnelli Anna, Piscosquito Giuseppe

Abstract excerpt

Peripheral nerves have peculiar energetic requirements because of considerable length of axons and therefore correct mitochondria functioning and distribution along nerves is fundamental. Mitochondrial dynamics refers to the continuous change in size, shape, and position of mitochondria within cells. Abnormalities of mitochondrial dynamics produced by mutations in proteins involved in mitochondrial fusion...

Read the complete abstract on PubMed

Topics

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

Share to Axonal Transport
Share to Charcot-Marie-Tooth Disease
Share to GDAP1 gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hereditary Sensory and Motor Neuropathy

Share to Mitochondria

Share to Mitochondrial Dynamics

Share to Mitochondrial Proteins

Share to Mutation

Source

Identifiers

PMID: 25847151
DOI: 10.1016/j.neulet.2015.04.001

Genes

GDAP1
MFN2
DNAJB2
HSPB1
HSPB3
HSPB8
NEFL
OPA1
TUBB3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mitochondrial dynamics and inherited peripheral nerve diseases.PMID 25847151Read ↗

Mitochondrial Dynamics in Peripheral NeuropathiesSemantic proximity Read ↗

Peripheral neuropathy in mitochondrial disease.Semantic proximity Read ↗

[Molecular pathogenesis of hereditary motor and sensory neuropathy].Semantic proximity Read ↗

Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations.Semantic proximity Read ↗

Impaired Mitochondrial Mobility in Charcot-Marie-Tooth DiseaseSemantic proximity Read ↗

Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A.Semantic proximity Read ↗

Mechanisms of disease and clinical features of mutations of the gene for mitofusin 2: an important cause of hereditary peripheral neuropathy with striking clinical variability in children and adults.Semantic proximity Read ↗

Inherited peripheral neuropathies due to mitochondrial disorders.Semantic proximity Read ↗

Axonal Charcot-Marie-Tooth Disease: from Common Pathogenic Mechanisms to Emerging Treatment Opportunities.Semantic proximity Read ↗

Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease.Semantic proximity Read ↗

MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives.Semantic proximity Read ↗

Abnormalities of Mitochondrial Dynamics in Neurodegenerative DiseasesSemantic proximity Read ↗

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