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Joseph Cao

Researcher at University of California, Los Angeles

Publications -  6
Citations -  1880

Joseph Cao is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: PINK1 & Parkin. The author has an hindex of 4, co-authored 6 publications receiving 1755 citations.

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Journal ArticleDOI

Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin.

TL;DR: Removal of Drosophila PINK1 homologue function results in male sterility, apoptotic muscle degeneration, defects in mitochondrial morphology and increased sensitivity to multiple stresses including oxidative stress, which underscores the importance of mitochondrial dysfunction as a central mechanism of Parkinson's disease pathogenesis.
Journal ArticleDOI

Loss-of-function analysis suggests that Omi/HtrA2 is not an essential component of the PINK1/PARKIN pathway in vivo.

TL;DR: It is shown that Omi/HtrA2 null mutants in Drosophila, in contrast to pink1 or parkin null mutants, do not show mitochondrial morphological defects and retains significant, if not full, function of Omi/, as well as expression of protease-compromised versions of the protein.
Journal ArticleDOI

Discovery-Based Science Education: Functional Genomic Dissection in Drosophila by Undergraduate Researchers

Jiong Chen, +146 more
- 15 Feb 2005 - 
TL;DR: The UCLA Undergraduate Consortium for Functional Genomics provides the answer to how to combine professional-quality research with discovery-based undergraduate education.
Journal ArticleDOI

Genomewide Clonal Analysis of Lethal Mutations in the Drosophila melanogaster Eye: Comparison of the X Chromosome and Autosomes

Gerald B. Call, +272 more
- 01 Oct 2007 - 
TL;DR: The data reveal the surprising result that the X chromosome has almost twice the frequency of essential genes involved in eye development as that found on the autosomes.
Book ChapterDOI

SUMO in Drosophila Development

TL;DR: The ability of SUMO and other ubiquitin-like proteins to diversify protein function may be critical to the evolution of developmental complexity.