Mark Hannink
Molecular Biology · 2003–2009
A researcher in the Science corpus: 5 papers; trusts 8 researchers and is trusted by 29 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 79 citations into it; #1,437 of 17,773 by trust here, #3,087 by citations
- Biochemistry — 24 citations into it
- Oncology — 5 citations into it
Whom Mark Hannink trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Mark Hannink overall
- Donna D. Zhang
- Masayuki Yamamoto
- Liam Baird
- A. Kobayashi
- James W. Kaspar
- H. Forman
- Makoto Kobayashi
- A. Dinkova-Kostova
- Lauren E Tebay
- Suresh Niture
Papers from Mark Hannink's perspective
Ordered by how strongly the researchers Mark Hannink trusts endorse each paper. Same corpus, a different order for every researcher.
- Structure of the Cul1–Rbx1–Skp1–F boxSkp2 SCF ubiquitin ligase complex (Nature)
- Oxidative Stress Sensor Keap1 Functions as an Adaptor for Cul3-Based E3 Ligase To Regulate Proteasomal Degradation of Nrf2 (Molecular and Cellular Biology)
- Enhanced Expression of the Transcription Factor Nrf2 by Cancer Chemopreventive Agents: Role of Antioxidant Response Element-Like Sequences in the nrf2 Promoter (Molecular and Cellular Biology)
- Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants (Proceedings of the National Academy of Sciences of the United States of America)
- Protection against electrophile and oxidant stress by induction of the phase 2 response: Fate of cysteines of the Keap1 sensor modified by inducers (Proceedings of the National Academy of Sciences of the United States of America)
- Molecular mechanism activating Nrf2-Keap1 pathway in regulation of adaptive response to electrophiles. (Free Radical Biology & Medicine)
- Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response (Nature Cell Biology)
- Distinct Cysteine Residues in Keap1 Are Required for Keap1-Dependent Ubiquitination of Nrf2 and for Stabilization of Nrf2 by Chemopreventive Agents and Oxidative Stress (Molecular and Cellular Biology)
- Biologically active sphingolipids in cancer pathogenesis and treatment (Nature Reviews. Cancer)
- Regulated translation initiation controls stress-induced gene expression in mammalian cells. (Molecules and Cells)
Their papers
- Distinct Cysteine Residues in Keap1 Are Required for Keap1-Dependent Ubiquitination of Nrf2 and for Stabilization of Nrf2 by Chemopreventive Agents and Oxidative Stress (2003) — 1,420 citations
- Nrf2 Is a Direct PERK Substrate and Effector of PERK-Dependent Cell Survival (2003) — 1,236 citations
- Keap1 Is a Redox-Regulated Substrate Adaptor Protein for a Cul3-Dependent Ubiquitin Ligase Complex (2004) — 1,258 citations
- CERAMIDE SYNTHASE 1 IS REGULATED BY PROTEASOMAL MEDIATED TURNOVER (2009) — 56 citations
- Stress-induced ER to Golgi translocation of ceramide synthase 1 is dependent on proteasomal processing (2009) — 45 citations