Boston, MA, United States of America

Jesse Gray


Average Co-Inventor Count = 12.0

ph-index = 1


Company Filing History:


Years Active: 2025

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1 patent (USPTO):Explore Patents

Title: Jesse Gray: Innovator in Nucleic Acid Trans-Splicing Molecules

Introduction

Jesse Gray is a notable inventor based in Boston, MA (US). He has made significant contributions to the field of genetic research, particularly in the development of nucleic acid trans-splicing molecules. His work aims to address critical genetic disorders, showcasing his commitment to advancing medical science.

Latest Patents

Jesse Gray holds a patent for ABCA4 trans-splicing molecules. This innovative patent involves nucleic acid trans-splicing molecules, such as pre-mRNA trans-splicing molecules and RNA exon editing molecules. These molecules are designed to correct mutations in the ABCA4 gene, which is crucial for treating disorders like ABCA4-associated retinal dystrophies, including Stargardt Disease and cone-rod dystrophy. The patent outlines methods for using these molecules to correct mutations and prepare medicaments for treating related disorders.

Career Highlights

Jesse Gray is currently associated with Ascidian Therapeutics, Inc., where he continues to push the boundaries of genetic research. His work has the potential to transform treatment options for patients suffering from genetic disorders linked to the ABCA4 gene. With a focus on innovative solutions, he is making strides in the field of biotechnology.

Collaborations

Jesse collaborates with talented individuals such as Rebekka Krumbach and Scott J Dooley. Their combined expertise enhances the research and development efforts at Ascidian Therapeutics, Inc., fostering an environment of innovation and discovery.

Conclusion

Jesse Gray's contributions to the field of genetic research through his patent on ABCA4 trans-splicing molecules highlight his role as a leading inventor. His work not only addresses significant medical challenges but also paves the way for future advancements in the treatment of genetic disorders.

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