Toll-like receptors TLR2 and TLR4 block the replication of pancreatic β cells in diet-induced obesity
Year: 2019
Type: article
Source: Nature Immunology
Institutions: Cornell University, University of Michigan, Michigan Medicine, Wayne State University, University of Colorado Anschutz, Brigham and Women's Hospital, Joslin Diabetes Center, Harvard University, Harvard Stem Cell Institute, University of Virginia, Vanderbilt University, Vanderbilt University Medical Center, XBiotech (United States), University of Pennsylvania, Wageningen University & Research
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funders: U.S. Department of Veterans Affairs, University of Michigan, Nature, National Institutes of Health, Weill Cornell Medical College, Medical School, University of Michigan, Japan Society for the Promotion of Science, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Arthritis and Musculoskeletal and Skin Diseases
Awards: G1203346010, G1238215490, University of Michigan Center for Gastrointestinal Research, G1404790370, G1619971191, Interplay Between SERPINB1 and TLR2/TLR4 in Beta Cell Regeneration, G301048564, G4270174501, G4440096208, G4541629867, G4599319085, G4787208505, Regulation of mitochondrial dynamics by ERAD, G5433717521, Role of SerpinB1 in beta cell growth, Secretory Pathway Protein Degradation Maintains Insulin Biogenesis + Secretion, G643119639, G803440102, G816019242, Heterogeneity of pancreatic islets, Molecular and Cellular Basis for Digestive Diseases, University of Michigan Rogel Cancer Center Support Grant 2023-2028, Integrated Islet Distribution Program (U24) - 2021, Michigan Diabetes Research Center (MDRC), Diabetes Research Center
OpenAlex ID: W2945399264