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Lipid Storage Disorders

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Small-Molecule Modulators of Lipid Storage for Treatment of Obesity, Atherosclerosis, Metabolic Syndrome and Lipid Storage Disea by nih.gov . There are also a number of inherited lipid storage diseases that result in harmful buildup of various lipids.... Advantages: Modulation of lipid droplet accumulation is a novel mechanism for treatment of lipid storage...

Cyclodextrins as Therapeutics for Lysosomal Storage Disorders by nih.gov (e.g., vitamin E), as therapeutics for the treatment of lysosomal storage disorders (LSDs) caused.... Applications: treatment of lysosomal storage diseases treatment of disorders caused by accumulation of non...

Biomarkers for Niemann-Pick Disease Type C and Related Disorders of Oxysterol Accumulation by nih.gov storage disorder characterized by liver disease and progressive neurodegeneration. Lysosomal storage..., including other lysosomal storage diseases, cholesterol trafficking diseases, and neurodegenerative diseases...

Novel Tocopherol and Tocopheryl Quinone Derivatives as Therapeutics for Lysosomal Storage Disorders by nih.gov size, and the treatment of lysosomal storage disorders (LSDs) are provided. The inventors... Derivatives as Therapeutics for Lysosomal Storage Disorders. For collaboration opportunities, please contact...

The antibiotic and DNA-transfecting peptide LAH4 selectively associates with, and disorders, anionic lipids in mixed membranes by Cheryl Patient Expert

has potential applications from basic research to gene therapeutic approaches for congenital disorders, cancer... LAH4. We therefore sought to determine whether anionic lipids, found in eukaryotic cells and presented...

Disorders of Lipid Metabolism: Trans Fat Facts by Diana Y. Healthy Living Professional

You may already know that saturated fats found in animal fat, like marbling in steak, sausage, cheese and butter can raise LDL cholesterol levels and clog arteries. Trans fat is similarly bad for our hearts. You should e

A Mouse Model for Systemic Inflammation in Glucocerebrosidase-Deficient Mice with Minimal Glucosylceramide Storage by nih.gov Description of Invention: Gaucher disease, the most common lysosomal storage disease, is an inherited metabolic disorder in which harmful quantities of the lipid glucocerebroside accumulate...

Genetics Home Reference: myosin storage myopathy by nih.gov of the disorder. It is unclear how these changes lead to muscle weakness in people with myosin storage myopathy... February 2013 What is myosin storage myopathy? Myosin storage myopathy is a condition...

Genetics Home Reference: glycogen storage disease type V by nih.gov disorder catalog What other names do people use for glycogen storage disease type V... Reviewed July 2010 What is glycogen storage disease type V? Glycogen storage disease type V...

Genetics Home Reference: glycogen storage disease type III by nih.gov September 2010 What is glycogen storage disease type III? Glycogen storage disease type III (also known as GSDIII or Cori disease) is an inherited disorder caused by the buildup of a complex sugar...