Related Experiment Videos

Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial complex I: genomic organization and expression

V Procaccio¹, P Lescuyer, I Bourges

¹Laboratoire BECP-EA2943 UJF/LRA6V CEA-DBMS, CEA Grenoble, 17 rue des Martyrs, 38054 Grenoble, cedex 9, France.

Mammalian Genome : Official Journal of the International Mammalian Genome Society

|September 1, 2000

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

The recurrent p.Glu3Lys variant in EHHADH is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalities.

Molecular genetics and metabolism reports·2025

Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathies.

Neuromuscular disorders : NMD·2022

Mitochondrial DNA content reduction in the most fertile spermatozoa is accompanied by increased mitochondrial DNA rearrangement.

Human reproduction (Oxford, England)·2022

Development of new genetic resources for faba bean (Vicia faba L.) breeding through the discovery of gene-based SNP markers and the construction of a high-density consensus map.

Scientific reports·2020

Therapeutic drug monitoring of imipenem and the incidence of toxicity and failure in hospitalized patients: a retrospective cohort study.

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases·2018

The mitochondrial DNA content of cumulus cells may help predict embryo implantation.

Journal of assisted reproduction and genetics·2018

See all related articles