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

Unsolved issues related to human mitochondrial diseases.

Biochimie - 1 May 2014

Lombès Anne, Auré Karine, Bellanné-Chantelot Christine, Gilleron Mylène, Jardel Claude

Abstract excerpt

Human mitochondrial diseases, defined as the diseases due to a mitochondrial oxidative phosphorylation defect, represent a large group of very diverse diseases with respect to phenotype and genetic causes. They present with many unsolved issues, the comprehensive analysis of which is beyond the scope of this review. We here essentially focus on the mechanisms underlying the diversity of targeted tissues, which is...

Read the complete abstract on PubMed

Topics

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

Share to Chimerism
Share to Genetic Heterogeneity
Share to Inheritance Patterns

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

Share to Mitochondria

Share to Mitochondrial Diseases

Share to Mitochondrial Proteins

Share to Mitosis

Share to Organ Specificity

Source

Identifiers

PMID: 23973280
DOI: 10.1016/j.biochi.2013.08.012

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

Unsolved issues related to human mitochondrial diseases.PMID 23973280Read ↗

[Pathophysiology of human mitochondrial diseases].Semantic proximity Read ↗

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease.Semantic proximity Read ↗

Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders.Semantic proximity Read ↗

Molecular genetic aspects of human mitochondrial disorders.Semantic proximity Read ↗

Mitochondrial genetics and human disease.Semantic proximity Read ↗

Diseases of the human mitochondrial oxidative phosphorylation system.Semantic proximity Read ↗

Mitochondrial DNA and disease.Semantic proximity Read ↗

Gaining Insight into Mitochondrial Genetic Variation and Downstream Pathophysiology: What Can i(PSCs) Do?Semantic proximity Read ↗

Clinical and molecular studies of mitochondrial disease.Semantic proximity Read ↗

Insight into mammalian mitochondrial DNA segregation.Semantic proximity Read ↗

[Diseases of the human mitochondrial oxidative phosphorylation system].Semantic proximity Read ↗

Cell identity and nucleo-mitochondrial genetic context modulate OXPHOS performance and determine somatic heteroplasmy dynamicsSemantic proximity Read ↗

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