Sort by
Refine Your Search
-
Country
-
Employer
- University of Washington
- FAPESP - São Paulo Research Foundation
- Pennsylvania State University
- The Ohio State University
- The University of Arizona
- University of Colorado
- Virginia Tech
- Yale University
- CNRS
- Duke University
- Indiana University
- Karolinska Institutet (KI)
- Loyola University
- St Jude Children's Research Hospital
- TTI
- University of California, Los Angeles
- University of Cambridge;
- University of Dundee
- University of Florida
- University of Hradec Kralove
- University of Hradec Králové
- University of Miami
- University of Minnesota
- University of Oxford
- University of Southern California
- University of São Paulo
- University of Utah
- Veterinärmedizinische Universität Wien (University of Veterinary Medicine Vienna)
- Wayne State University
- 19 more »
- « less
-
Field
-
signaling and metabolic vulnerability in metastatic cancer. Our goal is to reveal how the mitochondrial metabolism and nutrient stress controls metastatic progression through metabolic reprogramming
-
our research is uncovering the molecular mechanisms of ATP-dependent AAA proteolytic machines, both soluble and membrane-spanning, and their accessory factors in bacterial and mitochondrial systems. We
-
metabolism, 2) the role of mRNA-binding proteins in cell regeneration, and 3) characterization of cellular and mitochondrial iron homeostasis. Using mouse models, histology, cell culture, differential
-
University of California, Los Angeles | Los Angeles, California | United States | about 12 hours ago
genomic damage in tissue aging and age-related pathology. The Vandiver lab uses emerging genomic technology, induced pluripotent cells and in vitro skin culture to test the impact of acquired mitochondrial
-
-mitochondrial axis connection or calibration of allergic immune responses by the gut microbiome. Mechanistic insights gained from this research would be applied to next-generation development of microbiota-based
-
). mTORC1 Regulates Mitochondrial Integrated Stress Response and Mitochondrial Myopathy Progression. Cell Metabolism 26, 419-428 e415. We are located in a modern research hub called NEO at Karolinska
-
-cell multi-omics approaches • Analysis of large-scale genomic and/or transcriptomic datasets • Experience with mitochondrial or innate immune/inflammation assays Overtime Status Exempt: Not eligible
-
muscle mass and function, histological and morphometric analyses, protein turnover, mitochondrial biology, metabolic assessment, or related approaches. · Experience with mammalian cell culture and
-
products, EPR or UV–Vis/fluorescence spectroscopy, mitochondrial function assays (e.g., Seahorse), and photoprotection studies will be considered an advantage but is not mandatory. Applications Applications
-
biliary atresia, alpha-1 antitrypsin deficiency, Alagille syndrome, mitochondrial hepatopathies, cystic fibrosis, NAFLD, parenteral nutrition-associated cholestasis, acute liver failure, chronic cholestatic