Michael Studer

ORCID: 0000-0002-6742-1921
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About
Contact & Profiles
Research Areas
  • RNA Research and Splicing
  • Stochastic processes and financial applications
  • RNA and protein synthesis mechanisms
  • DNA Repair Mechanisms
  • Insurance, Mortality, Demography, Risk Management
  • CRISPR and Genetic Engineering
  • Coenzyme Q10 studies and effects
  • Adipose Tissue and Metabolism
  • Endoplasmic Reticulum Stress and Disease
  • Heat shock proteins research
  • Financial Risk and Volatility Modeling
  • Risk and Portfolio Optimization

ETH Zurich
2001-2023

RNA helicases of the DEAH/RHA family are involved in many essential cellular processes, such as splicing or ribosome biogenesis, where they remodel large RNA-protein complexes to facilitate transitions next intermediate. DEAH couple adenosine triphosphate (ATP) hydrolysis conformational changes their catalytic core. This movement results translocation along RNA, which is held place by auxiliary C-terminal domains. The activity proteins strongly enhanced and diverse class G-patch activators....

10.1073/pnas.1913880117 article EN cc-by-nc-nd Proceedings of the National Academy of Sciences 2020-03-16

10.1016/s0167-6687(03)00152-5 article EN Insurance Mathematics and Economics 2003-08-01

SUMMARY The spliceosome is a staggeringly complex machine comprising, in humans, 5 snRNAs and >150 proteins. We scaled haploid CRISPR-Cas9 base editing to target the entire human interrogated mutants using U2 snRNP/SF3b inhibitor, pladienolide B. Hypersensitive substitutions define functional sites U1/U2-containing A-complex but also components that act as late second chemical step after SF3b dissociated. Viable resistance map not only B binding site G-patch (ATPase activator) domain of...

10.1101/2022.11.13.516350 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-11-16
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