What is he best known for?
The fields of study he is best known for:
His main research concerns Cell biology, Autophagy database, Vacuole, Biochemistry and Autophagy-Related Protein 8 Family.
The various areas that he examines in his Autophagy database study include Peroxisome degradation, Hansenula polymorpha, Autolysosome, Chaperone-mediated autophagy and Neuroscience.
His Autolysosome study combines topics from a wide range of disciplines, such as Sequestosome 1 and Physiology.
His Vacuole study integrates concerns from other disciplines, such as Lysosome and CVT pathway.
The study incorporates disciplines such as Cytoplasm-to-vacuole targeting and Computational biology in addition to Autophagy-Related Protein 8 Family.
His work carried out in the field of Bioinformatics brings together such families of science as BECN1, Autophagy-Related Protein 7, Autophagosome maturation, Autophagosome membrane and MAP1LC3B.
His most cited work include:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- Guidelines for the use and interpretation of assays for monitoring autophagy (3242 citations)
- Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes (1951 citations)
What are the main themes of his work throughout his whole career to date?
Michael Thumm mostly deals with Cell biology, Biochemistry, Vacuole, Saccharomyces cerevisiae and Yeast.
His Cell biology research is multidisciplinary, relying on both ATG8, Biogenesis, CVT pathway, Vesicle and Autophagosome.
Michael Thumm has researched Autophagosome in several fields, including MAP1LC3B, Chaperone-mediated autophagy and Computational biology.
His Vacuole research includes elements of Cytoplasm-to-vacuole targeting and Lysosome.
His research in Saccharomyces cerevisiae intersects with topics in BAG3, Botany and Proteasome.
He combines subjects such as Autophagosome membrane, Neuroscience, Autophagosome maturation and Autophagy-Related Protein 7 with his study of Autolysosome.
He most often published in these fields:
- Cell biology (64.79%)
- Biochemistry (49.30%)
- Vacuole (33.80%)
What were the highlights of his more recent work (between 2012-2021)?
- Cell biology (64.79%)
- Biophysics (8.45%)
- Phosphoinositide binding (5.63%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Cell biology, Biophysics, Phosphoinositide binding, Autophagosome and ATG8.
His biological study spans a wide range of topics, including Ubiquitin ligase, Saccharomyces cerevisiae and Mitophagy.
His Ubiquitin ligase research is multidisciplinary, incorporating elements of ATG5 and Autophagy-Related Protein 8 Family.
His research investigates the connection between Biophysics and topics such as Vacuole that intersect with problems in Membrane contact site and Nuclear pore.
His Autophagosome study combines topics in areas such as Biogenesis, BECN1, MAP1LC3B, Sequestosome 1 and Physiology.
His study in ATG8 is interdisciplinary in nature, drawing from both Lipid-anchored protein and Autophagosome formation.
Between 2012 and 2021, his most popular works were:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- PI3P binding by Atg21 organises Atg8 lipidation (42 citations)
- Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356 (40 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Cell biology, Chaperone-mediated autophagy, Autolysosome, Computational biology and Autophagosome.
His Cell biology research includes themes of ATG8 and ATG5.
His Chaperone-mediated autophagy research is multidisciplinary, incorporating perspectives in Multicellular organism and Physiology.
His studies deal with areas such as MAP1LC3B, Sequestosome 1 and BECN1 as well as Autolysosome.
His Autophagosome research incorporates elements of Plasma protein binding, Biogenesis and Ubiquitin ligase, Ubiquitin-conjugating enzyme.
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