Sökning: "UCP2"
Visar resultat 1 - 5 av 18 avhandlingar innehållade ordet UCP2.
1. Islet insulin secretory patterns in diabetes and the role of UCP2
Sammanfattning : During development of type 1 and type 2 diabetes plasma insulin patterns are altered. Since the islet insulin release pattern has been implicated in this development, insulin secretion from single islets was studied and linked to the islet protein levels of uncoupling protein-2 (UCP2). LÄS MER
2. Genetics of type 2 diabetes and the metabolic syndrome
Sammanfattning : Type 2 diabetes and the metabolic syndrome are highly prevalent disorders with severe complications such as cardiovascular disease. The aetiology of type 2 diabetes and the metabolic syndrome is not known, but the interaction between genetic factors and environmental triggers is important. LÄS MER
3. Molecular mechanisms of weight regulation in obesity and chronic renal failure with special reference to leptin and uncoupling protein 2
Sammanfattning : Obesity, which increases the risk of developing serious medical disorders, such as cardiovascular disease and diabetes, is threatening to become a global epidemic, meaning escalating healthcare costs for society and reduced quality of life for the individual. Thus, there is a large unmet need for improved preventive strategies and effective treatments. LÄS MER
4. On obesity in acute pancreatitis
Sammanfattning : Over-nutrition is one of today s most visible public health problems. Currently over 40% of the Swedish population is either overweight or obese. Acute pancreatitis (AP) is an acute inflammatory process of the pancreas with variable involvement of regional tissues and/or remote organ systems. LÄS MER
5. Molecular mechanisms of aging in MTDNA mutator mice
Sammanfattning : Mitochondria are intensely studied in the field of aging. mtDNA mutator mice have a proofreading deficiency in the mitochondrial DNA polymerase POLG, which causes a large amount of point mutations to be accumulated in mitochondrial DNA. These mice have mitochondrial dysfunction and experience a range of premature aging phenotypes. LÄS MER