Member of the Association of American Physicians
Tobias B. Huber mainly investigates Cell biology, Podocyte, Internal medicine, Endocrinology and Slit diaphragm. His Cell biology study integrates concerns from other disciplines, such as Autophagy and Cellular differentiation. His study in the fields of Synaptopodin under the domain of Podocyte overlaps with other disciplines such as Fusion protein.
He combines subjects such as Diabetes mellitus and Kinase with his study of Internal medicine. His research integrates issues of mTORC1 and PI3K/AKT/mTOR pathway in his study of Endocrinology. His study in Slit diaphragm is interdisciplinary in nature, drawing from both Podocyte foot, Podocin, Nephrin, Immunoglobulin domain and Molecular biology.
The scientist’s investigation covers issues in Cell biology, Podocyte, Internal medicine, Kidney and Endocrinology. The various areas that Tobias B. Huber examines in his Cell biology study include Autophagy, Nephrin and Cytoskeleton. Tobias B. Huber focuses mostly in the field of Podocyte, narrowing it down to topics relating to Glomerulosclerosis and, in certain cases, Focal segmental glomerulosclerosis.
His Kidney research includes themes of Cancer research, Immunology, Kidney disease and Pathology. Endocrinology is closely attributed to mTORC1 in his study. The concepts of his Slit diaphragm study are interwoven with issues in Podocyte foot and Podocin.
His primary areas of investigation include Cell biology, Podocyte, Kidney, Internal medicine and Severe acute respiratory syndrome coronavirus 2. His Cell biology research integrates issues from Autophagy, Transgene, Gene knockdown, Receptor and Cell type. When carried out as part of a general Autophagy research project, his work on Chaperone-mediated autophagy and Autolysosome is frequently linked to work in Set and Knowledge base, therefore connecting diverse disciplines of study.
His studies deal with areas such as Glomerulosclerosis, Immune system, Focal segmental glomerulosclerosis and Membranous nephropathy as well as Podocyte. His Kidney research is multidisciplinary, relying on both Biomarker discovery and Pathology. The Internal medicine study combines topics in areas such as Endocrinology and Epithelial sodium channel.
Tobias B. Huber mostly deals with Cell biology, Severe acute respiratory syndrome coronavirus 2, Kidney disease, Autophagy and Pandemic. His Cell biology study combines topics from a wide range of disciplines, such as Human kidney, Transgene and Human brain. Tobias B. Huber has researched Autophagy in several fields, including Tyrosine, Myeloid leukemia, Mutant and Phosphorylation.
His Internal medicine research is multidisciplinary, incorporating perspectives in Epithelial sodium channel and Sodium. In his work, Podocyte is strongly intertwined with Genetically modified mouse, which is a subfield of Pathology. His Podocyte study frequently intersects with other fields, such as PI3K/AKT/mTOR pathway.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
Daniel J. Klionsky;Amal Kamal Abdel-Aziz;Sara Abdelfatah;Mahmoud Abdellatif.
Autophagy (2021)
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin.
Autophagy (2016)
Guidelines for the use and interpretation of assays for monitoring autophagy
Daniel J. Klionsky;Fabio C. Abdalla;Hagai Abeliovich;Robert T. Abraham.
Autophagy (2012)
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
Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin.
Autophagy (2016)
Multiorgan and Renal Tropism of SARS-CoV-2.
Victor G. Puelles;Marc Lütgehetmann;Maja T. Lindenmeyer;Jan P. Sperhake.
The New England Journal of Medicine (2020)
Autophagy influences glomerular disease susceptibility and maintains podocyte homeostasis in aging mice
Björn Hartleben;Markus Gödel;Catherine Meyer-Schwesinger;Shuya Liu.
Journal of Clinical Investigation (2010)
Mitochondrial Dynamics Controls T Cell Fate through Metabolic Programming
Michael D D. Buck;Michael D D. Buck;David O'Sullivan;Ramon I I. Klein Geltink;Jonathan D D. Curtis.
Cell (2016)
Role of mTOR in podocyte function and diabetic nephropathy in humans and mice
Markus Gödel;Björn Hartleben;Nadja Herbach;Shuya Liu.
Journal of Clinical Investigation (2011)
mTORC1 activation in podocytes is a critical step in the development of diabetic nephropathy in mice
Ken Inoki;Hiroyuki Mori;Junying Wang;Tsukasa Suzuki.
Journal of Clinical Investigation (2011)
Nephrin and CD2AP associate with phosphoinositide 3-OH kinase and stimulate AKT-dependent signaling.
Tobias B. Huber;Björn Hartleben;Jeong Kim;Miriam Schmidts.
Molecular and Cellular Biology (2003)
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