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Brett P. Monia

Researcher at Isis Pharmaceuticals

Publications -  214
Citations -  10319

Brett P. Monia is an academic researcher from Isis Pharmaceuticals. The author has contributed to research in topics: Oligonucleotide & Transthyretin. The author has an hindex of 46, co-authored 214 publications receiving 9317 citations. Previous affiliations of Brett P. Monia include Harvard University & University of Texas Southwestern Medical Center.

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Inhibiting triglyceride synthesis improves hepatic steatosis but exacerbates liver damage and fibrosis in obese mice with nonalcoholic steatohepatitis.

TL;DR: Results from this mouse model would suggest accumulation of triglycerides may be a protective mechanism to prevent progressive liver damage in NAFLD.
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Antisense oligonucleotide therapy for neurodegenerative disease

TL;DR: Treatment initiated near onset significantly slowed disease progression in a model of amyotrophic lateral sclerosis caused by a mutation in SOD1, suggesting that direct delivery of antisense oligonucleotides could be an effective, dosage-regulatable means of treating neurodegenerative diseases, including ALS, where appropriate target proteins are known.
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Inhibition of protein kinase Cε prevents hepatic insulin resistance in nonalcoholic fatty liver disease

TL;DR: The hypothesis that PKCepsilon plays a critical role in mediating fat-induced hepatic insulin resistance and represents a novel therapeutic target for type 2 diabetes is supported.
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Reversal of diet-induced hepatic steatosis and hepatic insulin resistance by antisense oligonucleotide inhibitors of acetyl-CoA carboxylases 1 and 2

TL;DR: In rats with NAFLD, suppression of both enzymes with a single ASO was required to significantly reduce hepatic malonyl-CoA levels in vivo, lower hepatic lipids, and improve hepatic insulin sensitivity, suggesting that pharmacological inhibition of Acc1 and -2 may be a novel approach in the treatment ofNAFLD.