St. Louis, MO, United States of America

Michael A Gitcho



Average Co-Inventor Count = 5.0

ph-index = 1

Forward Citations = 3(Granted Patents)


Company Filing History:


Years Active: 2014-2020

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3 patents (USPTO):Explore Patents

Title: Michael A Gitcho: Innovator in TDP-43 Proteinopathy Research

Introduction

Michael A Gitcho, based in St. Louis, MO, is a notable inventor recognized for his contributions to the field of biomedical research. With three registered patents, he has focused on advancing methods for the identification and treatment of TDP-43 proteinopathies, conditions that have significant implications for neurodegenerative diseases.

Latest Patents

Among his latest innovations, Gitcho holds a pivotal patent titled "Sequences associated with TDP-43 proteinopathies and methods of using the same." This invention details nucleic acids and peptides that serve as tools for identifying subjects at risk for TDP-43 proteinopathy, significantly contributing to early detection and potential therapeutic avenues. The patent also describes an array comprised of these nucleic acids and peptides, showcasing Gitcho's ability to blend cutting-edge science with practical applications.

Career Highlights

Michael Gitcho is currently affiliated with Washington University, where he continues to push the boundaries of research in neurodegeneration. His work has not only yielded patents but has also laid the groundwork for further inquiries into the complexities of proteinopathies, impacting both clinical and research practices.

Collaborations

Gitcho collaborates with esteemed colleagues such as Nigel J Cairns and Robert H Baloh, working together to explore innovative solutions in the realm of neurodegenerative disease research. These partnerships enrich his research and broaden the scope of inquiry within the scientific community.

Conclusion

Michael A Gitcho exemplifies the spirit of innovation in the biomedical field. Through his patents and collaborative efforts, he is making significant strides in understanding TDP-43 proteinopathies, contributing invaluable knowledge that may lead to enhanced diagnostic and therapeutic strategies.

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