S. Hess
Spectroscopy · with Chan · 2011–2015
A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Spectroscopy — 9 citations into it
Whom S. Hess trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Matthias Mann (in Spectroscopy)
Papers from S. Hess's perspective
Ordered by how strongly the researchers S. Hess trusts endorse each paper. Same corpus, a different order for every researcher.
- Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin (Nature)
- PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1 (Nature Cell Biology)
- Parkin is recruited selectively to impaired mitochondria and promotes their autophagy (Journal of Cell Biology)
- PINK1-dependent recruitment of Parkin to mitochondria in mitophagy (Proceedings of the National Academy of Sciences of the United States of America)
- Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase (Nature Genetics)
- PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin (PLoS Biology)
- Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin (Nature)
- Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants (Proceedings of the National Academy of Sciences of the United States of America)
- Stable Isotope Labeling by Amino Acids in Cell Culture, SILAC, as a Simple and Accurate Approach to Expression Proteomics* (Molecular & Cellular Proteomics)
- Drosophila Parkin requires PINK1 for mitochondrial translocation and ubiquitinates Mitofusin (Proceedings of the National Academy of Sciences of the United States of America)
Their papers
- Broad activation of the ubiquitin–proteasome system by Parkin is critical for mitophagy (2011) — 998 citations
- The Xist lncRNA directly interacts with SHARP to silence transcription through HDAC3 (2015) — 714 citations