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Volumn 197, Issue 2, 2008, Pages 251-263
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Prominent pancreatic endocrinopathy and altered control of food intake disrupt energy homeostasis in prion diseases
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Author keywords
[No Author keywords available]
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Indexed keywords
GLUCAGON;
GLUCOSE;
INSULIN;
KETONE DERIVATIVE;
LEPTIN;
PRION PROTEIN;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANIMAL TISSUE;
ARTICLE;
CONTROLLED STUDY;
ENERGY BALANCE;
FLUID INTAKE;
FOOD INTAKE;
GLUCAGON BLOOD LEVEL;
GLUCAGON RELEASE;
GLUCOSE BLOOD LEVEL;
HAMSTER;
HOMEOSTASIS;
HYPERGLUCAGONEMIA;
HYPERGLYCEMIA;
HYPERINSULINEMIA;
HYPERLEPTINEMIA;
HYPERPHAGIA;
HYPOGLYCEMIA;
INSULIN BLOOD LEVEL;
MALE;
NONHUMAN;
PANCREAS ISLET DISEASE;
POLYDIPSIA;
PRION DISEASE;
PRIORITY JOURNAL;
PROTEIN BLOOD LEVEL;
SATIETY;
SCRAPIE AGENT;
STRAIN DIFFERENCE;
TRANSMISSIBLE MINK ENCEPHALOPATHY AGENT;
VIRUS STRAIN;
WEIGHT GAIN;
WEIGHT REDUCTION;
ANIMALS;
BLOOD GLUCOSE;
BODY WEIGHT;
CRICETINAE;
DRINKING;
EATING;
ENERGY METABOLISM;
GLUCAGON;
GLUCOSE TOLERANCE TEST;
HOMEOSTASIS;
HYPOTHALAMUS;
INSULIN;
LEPTIN;
MALE;
MESOCRICETUS;
PANCREATIC DISEASES;
PRION DISEASES;
PRPSC PROTEINS;
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EID: 43849085313
PISSN: 00220795
EISSN: 14796805
Source Type: Journal
DOI: 10.1677/JOE-07-0516 Document Type: Article |
Times cited : (13)
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References (55)
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