M. Lazarou
Epidemiology · 2010–2018
A researcher in the Science corpus: 6 papers; trusts 6 researchers and is trusted by 4 researchers here, as inferred from the citation graph.
Subfields
- Epidemiology — 99 citations into it; #908 of 2,148 by trust here, #394 by citations
- Molecular Biology — 96 citations into it; #11,936 of 17,773 by trust here, #5,655 by citations
- Neurology — 56 citations into it; #1,210 of 1,455 by trust here, #440 by citations
- Cell Biology — 28 citations into it
Whom M. Lazarou trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts M. Lazarou overall
- Nicole Exner
- T. Nguyen
- Gian-Luca McLelland
- Gabriele Zaffagnini
- A. Ordureau
- R. Youle
- A. Lutz
- Mashun Onishi
- B. Padman
- M. Fricker
Papers from M. Lazarou's perspective
Ordered by how strongly the researchers M. Lazarou trusts endorse each paper. Same corpus, a different order for every researcher.
- Parkin is recruited selectively to impaired mitochondria and promotes their autophagy (Journal of Cell Biology)
- PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1 (Nature Cell Biology)
- PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin (PLoS Biology)
- Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin (Nature)
- Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin (Nature)
- PINK1-dependent recruitment of Parkin to mitochondria in mitophagy (Proceedings of the National Academy of Sciences of the United States of America)
- Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused by inactivation of Drosophila Pink1 is rescued by Parkin. (Proceedings of the National Academy of Sciences of the United States of America)
- Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants (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)
- Mitochondrial Dysfunction and Oxidative Damage in parkin-deficient Mice* (Journal of Biological Chemistry)
Their papers
- The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy (2015) — 2,558 citations
- Role of PINK1 binding to the TOM complex and alternate intracellular membranes in recruitment and activation of the E3 ligase Parkin (2012) — 654 citations
- Atg8 family LC3/GABARAP proteins are crucial for autophagosome–lysosome fusion but not autophagosome formation during PINK1/Parkin mitophagy and starvation (2016) — 595 citations
- BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosis (2018) — 936 citations
- Deciphering the Molecular Signals of PINK1/Parkin Mitophagy. (2016) — 644 citations
- Mitochondrial membrane potential regulates PINK1 import and proteolytic destabilization by PARL (2010) — 1,343 citations