Urbana, IL, United States of America

Long M Luu



Average Co-Inventor Count = 3.0

ph-index = 1

Forward Citations = 3(Granted Patents)


Company Filing History:


Years Active: 2016-2019

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2 patents (USPTO):Explore Patents

Title: Long M Luu: Innovator in Myotonic Dystrophy Research

Introduction

Long M Luu is a prominent inventor based in Urbana, IL (US), known for his significant contributions to the field of therapeutic agents for myotonic dystrophy. With a total of 2 patents, his work focuses on innovative solutions for treating this challenging neuromuscular disease.

Latest Patents

Luu's latest patents include groundbreaking inventions aimed at addressing myotonic dystrophy. One patent describes bisamidinium-based inhibitors that provide compounds, compositions, and therapeutic methods for the treatment of myotonic dystrophy. These compounds selectively bind to CUG repeats in RNA or CTG repeats in DNA, inhibiting the replication of nucleic acids. The therapeutic agents are designed to target myotonic dystrophy type 1 (DM1) and have shown promising results in correcting misregulated alternative splicing in DM1 model cells. Another patent focuses on rationally designed multi-targeting therapeutic agents that address the pathobiology of DM1 in three distinct ways, including binding the expanded trinucleotide repeat and cleaving the toxic CUG in an RNase-like manner.

Career Highlights

Long M Luu is affiliated with the University of Illinois, where he conducts his research and develops innovative therapeutic solutions. His work has garnered attention for its potential to significantly improve the lives of individuals affected by myotonic dystrophy.

Collaborations

Luu collaborates with esteemed colleagues, including Steven C Zimmerman and Lien T T Nguyen, to advance research in this critical area of health.

Conclusion

Long M Luu's innovative work in developing therapeutic agents for myotonic dystrophy showcases his commitment to addressing complex medical challenges. His contributions are paving the way for new treatment options that could transform the lives of those affected by this condition.

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