Ann Arbor, MI, United States of America

David C Dawson


Average Co-Inventor Count = 4.0

ph-index = 1

Forward Citations = 12(Granted Patents)


Company Filing History:


Years Active: 1995

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1 patent (USPTO):Explore Patents

Title: David C Dawson: Innovator in Cystic Fibrosis Treatment

Introduction

David C Dawson is a notable inventor based in Ann Arbor, MI (US). He has made significant contributions to the field of medical research, particularly in the treatment of cystic fibrosis, a severe genetic disorder. His innovative approach has opened new avenues for therapeutic interventions.

Latest Patents

David C Dawson holds a patent for a method of testing potential cystic fibrosis treating compounds. This invention addresses the challenges posed by cystic fibrosis, which is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. His patent outlines a method that utilizes naturally-occurring CFTR mutants to evaluate the effectiveness of compounds that elevate cAMP levels, thereby enhancing Cl conductance to near wild type levels. This breakthrough has the potential to improve treatment options for patients suffering from this debilitating condition.

Career Highlights

Dawson's career is marked by his dedication to advancing medical science through innovative research. He is affiliated with the University of Michigan, where he continues to explore new methodologies for treating genetic diseases. His work has garnered attention for its potential impact on patient care and treatment efficacy.

Collaborations

David C Dawson has collaborated with esteemed colleagues in the field, including Francis S Collins and Mitchell L Drumm. These partnerships have enriched his research and contributed to the development of effective treatment strategies for cystic fibrosis.

Conclusion

David C Dawson's contributions to cystic fibrosis research exemplify the importance of innovation in medical science. His patent and ongoing work at the University of Michigan highlight his commitment to improving the lives of those affected by genetic disorders.

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