Dallas, TX, United States of America

Yi-Li Min

USPTO Granted Patents = 1 

Average Co-Inventor Count = 3.0

ph-index = 1

Forward Citations = 1(Granted Patents)


Company Filing History:


Years Active: 2020

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1 patent (USPTO):Explore Patents

Title: **Innovator Spotlight: Yi-Li Min and His Contributions to Duchenne Muscular Dystrophy Research**

Introduction

Yi-Li Min, based in Dallas, TX, is an innovative inventor known for his contributions to medical research, particularly in the field of gene therapy for Duchenne muscular dystrophy (DMD). With one patent to his name, Min is making strides in the development of therapeutic strategies for this debilitating genetic disorder that affects 1 in 5,000 male births.

Latest Patents

Yi-Li Min's notable patent is titled "Generation and correction of a humanized mouse model with a deletion of dystrophin exon 44." This patent outlines a unique 'humanized' mouse model which serves as an invaluable tool for testing various strategies aimed at addressing DMD. The model can be used to evaluate CRISPR/Cas9 oligonucleotides, small molecules, and other therapies designed to promote exon skipping or introduce micro dystrophin mini-genes, paving the way for potential cell-based treatments.

Career Highlights

Min works at the University of Texas System, where he engages in groundbreaking research to provide solutions for the genetic deficiencies causing DMD. His work focuses extensively on methods for restoring the reading frame of exon 44 deletion through CRISPR-mediated techniques, which holds promise for treating patients directly. The potential impact of his work emphasizes the revolutionary nature of gene editing in permanently correcting mutations associated with DMD.

Collaborations

Throughout his career, Yi-Li Min has collaborated with esteemed colleagues such as Rhonda Bassel-Duby and Eric N Olson. These partnerships enrich his research, fostering a collaborative environment that encourages innovation in tackling DMD and other genetic disorders.

Conclusion

Yi-Li Min is making significant contributions to the understanding and treatment of Duchenne muscular dystrophy through his innovative research. With his pioneering work in developing 'humanized' mouse models and utilizing cutting-edge CRISPR technology, he is positioning himself as a key player in the field of genetic therapies. His efforts not only highlight the importance of collaboration in scientific research but also embody the spirit of innovation that drives advancements in medicine.

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