Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

A debut for mito-mouse

E A Shoubridge

    Nature Genetics
    |October 4, 2000
    PubMed
    Summary

    No abstract available in PubMed .

    Related Experiment Videos

    Related Concept Videos

    You might also read

    Related Articles

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

    Sort by
    Same author

    CHCHD10<sup>P80L</sup> knock-in zebrafish display a mild ALS-like phenotype.

    Experimental neurology·2024
    Same author

    Maternal segmental disomy in Leigh syndrome with cytochrome c oxidase deficiency caused by homozygous SURF1 mutation.

    Neuropediatrics·2006
    Same author

    Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome.

    Journal of medical genetics·2004
    Same author

    Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts.

    Human molecular genetics·2001
    Same author

    Selection of a mtDNA sequence variant in hepatocytes of heteroplasmic mice is not due to differences in respiratory chain function or efficiency of replication.

    Human molecular genetics·2001
    Same author

    Nuclear genetic defects of oxidative phosphorylation.

    Human molecular genetics·2001
    Same journal

    Mutational scanning reveals substrate-assisted autoregulation of the WNT destruction complex.

    Nature genetics·2026
    Same journal

    Spatial transcriptomic analyses highlight distinct erythroid niches in mice and humans.

    Nature genetics·2026
    Same journal

    Building up pangenome analysis block by block.

    Nature genetics·2026
    Same journal

    Mutations in splicing factor gene U2AF1 rescue defective oncogene splicing in KRAS-mutant cancers.

    Nature genetics·2026
    Same journal

    Assessing the effect of immune surveillance on clonal expansions in the blood.

    Nature genetics·2026
    Same journal

    Improved heritability partitioning and enrichment analyses using summary statistics with graphREML.

    Nature genetics·2026
    See all related articles