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Sarah J Richardson Islet Biology Group, Exeter Centre for Excellence in Diabetes (EXCEED), Institute of Biomedical and Clinical Sciences (IBCS), University of Exeter, RILD Level 4, Exeter, UK

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Alberto Pugliese Division of Diabetes Endocrinology and Metabolism, Departments of Medicine, Microbiology and Immunology, Diabetes Research Institute, Leonard Miller School of Medicine, University of Miami, Miami, Florida, USA

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.30 ) Denroche HC Verchere CB 2018 IAPP and type 1 diabetes: implications for immunity, metabolism and islet transplants . Journal of Molecular Endocrinology 60 R57– R75 . ( https://doi.org/10.1530/JME-17-0138 ) Dotta F Censini S Van Halteren AG

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Jennifer Chen The Westmead Institute for Medical Research, The University of Sydney Westmead Hospital, New South Wales, Australia

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Jenny E Gunton The Westmead Institute for Medical Research, The University of Sydney Westmead Hospital, New South Wales, Australia
Department of Endocrinology and Diabetes, Westmead Hospital, Sydney, New South Wales, Australia
Garvan Institute of Medical Research, Sydney, New South Wales, Australia
St Vincent’s Clinical School, University of New South Wales, Sydney, New South Wales, Australia

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Metabolism 5 233 – 244 . ( https://doi.org/10.1016/j.molmet.2016.01.002 ) Aguayo-Mazzucato C Bonner-Weir S 2018 Pancreatic β cell regeneration as a possible therapy for diabetes . Cell Metabolism 27 57 – 67 . ( https://doi.org/10.1016/j

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Emma Ahlqvist Department of Clinical Sciences, Malmö , Lund University, Malmö, Sweden

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Rashmi B Prasad Department of Clinical Sciences, Malmö , Lund University, Malmö, Sweden
Institute for Molecular Medicine Finland (FIMM), Helsinki University, Helsinki, Finland

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Leif Groop Department of Clinical Sciences, Malmö , Lund University, Malmö, Sweden
Institute for Molecular Medicine Finland (FIMM), Helsinki University, Helsinki, Finland

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metabolism regulating glucose is disrupted, but this can be the consequence of multiple different metabolic processes which can vary between individuals ( American Diabetes Association 2021 ). While some of these processes influence disease progression, drug

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Jennifer M Ikle Division of Endocrinology, Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA

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Anna L Gloyn Division of Endocrinology, Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA
Stanford Diabetes Research Center, Stanford University, Stanford, California, USA

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regulate the gene expression important for both pancreatic islet-cell development as well as glucose metabolism, including the insulin gene itself ( Yamagata et al. 1996 a ). Patients with heterozygous loss-of-function mutations in HNF4A have a

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Pieter-Jan Martens Clinical and Experimental Endocrinology (CEE), KU Leuven, Belgium

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Conny Gysemans Clinical and Experimental Endocrinology (CEE), KU Leuven, Belgium

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Chantal Mathieu Clinical and Experimental Endocrinology (CEE), KU Leuven, Belgium

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Beta cells persist in T1D pancreata without evidence of ongoing beta-cell turnover or neogenesis . Journal of Clinical Endocrinology and Metabolism 102 2647 – 2659 . ( https://doi.org/10.1210/jc.2016-3806 ) Lampeter EF Homberg M Quabeck K

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