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. 2016 Jun;57(6):925–942. doi: 10.1194/jlr.R066944

TABLE 1.

Clinical and molecular phenotypes studied in the HMDP resource

Trait Diet
Plasma lipids C, HF, ATH
Adiposity C, HF, ATH
Osteoporosis C
Blood cell levels C, HF, ATH
IR C, HF, ATH
Fatty liver disease HF, ATH
Heart failure induced by isoproterenol ISO
Atherosclerosis ATH
Diabetic nephropathy C
Transcript levels
 Liver C, HF, ATH
 Adipose C, HF
 Aorta ATH
 Hippocampus C
 Striatum C
 Skeletal muscle HF
 Heart C, ISO
Protein levels, liver C
Metabolites
 Liver C
 Plasma HF, ATH
Gut microbiome C, HF ATH
DNA methylation C

Mice were maintained on chow (C), high-fat (HF), or atherogenic (ATH) diets or treated with ISO.

HHS Vulnerability Disclosure