Location History:
- Reno, NV (US) (2018)
- Sparks, NV (US) (2012 - 2020)
Company Filing History:
Years Active: 2012-2020
Title: The Innovative Contributions of Dean Burkin in Treating Muscular Dystrophy
Introduction
Dean Burkin is a distinguished inventor based in Sparks, NV, recognized for his significant contributions to medical science, particularly in the treatment of muscular dystrophy. With a total of 13 patents to his name, Burkin has demonstrated an enduring commitment to advancing healthcare solutions through innovative approaches.
Latest Patents
Among his most recent patents, Burkin has developed methods for treating muscular dystrophy utilizing α7β1 integrin modulatory agents. The disclosed methods include administering an effective dosage of these agents to increase α7β1 integrin expression or activity in subjects suffering from muscular dystrophy. This innovative approach not only aims to treat the condition but also encompasses methods for enhancing muscle regeneration, repair, and maintenance, while prospectively preventing muscle injury or damage.
Career Highlights
Burkin’s career, prominently linked with the University of Nevada, showcases his dedication to research and innovation in the medical field. His persistent efforts in the realm of muscular dystrophy have positioned him as a vital contributor to biotechnological advancements aimed at improving patient outcomes.
Collaborations
Working alongside talented colleagues such as Ryan Wuebbles and Pam Van Ry, Burkin has fostered a collaborative environment that pushes the boundaries of research. Together, they contribute to a dynamic research atmosphere at the University of Nevada, encouraging innovation and discovery in medical treatments.
Conclusion
Dean Burkin's dedication to addressing muscular dystrophy through innovative patenting underscores the profound impact of scientific research and collaboration within the medical community. His work is a testament to the importance of developing novel therapeutic methods, aimed at improving the quality of life for those affected by muscular dystrophy and similar conditions.