What is he best known for?
The fields of study he is best known for:
- Cell membrane
- Apoptosis
- Biochemistry
Andreas Brech focuses on Cell biology, Autophagy, Endosome, ESCRT and Endocytic cycle.
His work deals with themes such as Biochemistry and BAG3, which intersect with Cell biology.
His research integrates issues of Cytoplasm, Programmed cell death, Intracellular and Cancer research in his study of Autophagy.
The various areas that he examines in his Endosome study include Microtubule, Endocytosis and TLR4.
Andreas Brech has researched Endocytic cycle in several fields, including Dynein, Kinesin, Endoplasmic reticulum and Cell membrane.
His work carried out in the field of Sequestosome-1 Protein brings together such families of science as MAP1LC3B, Nuclear protein and Sequestosome 1.
His most cited work include:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3242 citations)
- p62/SQSTM1 Binds Directly to Atg8/LC3 to Facilitate Degradation of Ubiquitinated Protein Aggregates by Autophagy (3020 citations)
- p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death (2330 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Cell biology, Endosome, Autophagy, Endocytic cycle and Endocytosis.
His studies deal with areas such as Receptor, Biochemistry and Vesicle as well as Cell biology.
Andreas Brech has included themes like Transport protein, Dynein, Epidermal growth factor and GTPase in his Endosome study.
His Autophagy study combines topics from a wide range of disciplines, such as Biophysics, Programmed cell death, Protein degradation and Cytoplasm.
Andreas Brech works mostly in the field of Endocytic cycle, limiting it down to concerns involving Phosphatidylinositol and, occasionally, Retromer.
He combines subjects such as Transferrin receptor, Internalization and Gap junction with his study of Endocytosis.
He most often published in these fields:
- Cell biology (120.86%)
- Endosome (54.60%)
- Autophagy (37.42%)
What were the highlights of his more recent work (between 2018-2021)?
- Cell biology (120.86%)
- Autophagy (37.42%)
- ESCRT (27.61%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Cell biology, Autophagy, ESCRT, Endosome and Biophysics.
Protein degradation, Microtubule, Retromer, Phosphatidylinositol and Lamin are subfields of Cell biology in which his conducts study.
His biological study spans a wide range of topics, including Anabolism, Motility, Wasting, Muscle atrophy and Metabolism.
His work in ESCRT tackles topics such as Membrane fission which are related to areas like Mitotic exit and Inner membrane.
His research in Endosome intersects with topics in Epithelium, GTPase and Mitophagy.
His work in Biophysics covers topics such as Receptor which are related to areas like Cell, Intracellular and Cell type.
Between 2018 and 2021, his most popular works were:
- Remodeling of secretory lysosomes during education tunes functional potential in NK cells (49 citations)
- ESCRT-mediated phagophore sealing during mitophagy. (37 citations)
- ESCRT-mediated phagophore sealing during mitophagy. (37 citations)
In his most recent research, the most cited papers focused on:
- Cell membrane
- Apoptosis
- Genetics
Andreas Brech mainly focuses on Cell biology, Autophagy, ESCRT, Mitophagy and Endosome.
In his works, he undertakes multidisciplinary study on Cell biology and Autophagy-related protein 13.
His study in Fragmentation is interdisciplinary in nature, drawing from both Membrane fission and Compartmentalization.
His Centriolar satellite research includes themes of Centriole, Microtubule, Mitosis and Chromosome segregation.
His Cell study combines topics in areas such as Receptor, Degranulation, Cytokine and Intracellular.
The various areas that Andreas Brech examines in his Cytokine study include Innate immune system and Cell type.
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