Edinburgh, United Kingdom

Rebekah Tillotson

USPTO Granted Patents = 1 

Average Co-Inventor Count = 4.0

ph-index = 1


Company Filing History:


Years Active: 2024

Loading Chart...
1 patent (USPTO):Explore Patents

Title: Rebekah Tillotson: Innovator in Genetic Therapeutics

Introduction

Rebekah Tillotson is a prominent inventor based in Edinburgh, GB. She has made significant contributions to the field of genetic therapeutics, particularly in the development of tools for expressing the MeCP2 protein. Her work is especially relevant for the treatment of disorders associated with reduced MeCP2 activity, such as Rett syndrome.

Latest Patents

Rebekah Tillotson holds a patent for "MeCP2 expression cassettes." This invention provides nucleic acid molecules that comprise a MeCP2 expression cassette. The expression cassette includes a 5′ transcriptional control region with a promoter capable of driving transcription in neural cells, an open reading frame encoding a MeCP2 protein, translation control signals, and a 3′ untranslated region (3′UTR) with various binding sites. The invention also includes viral vectors, particularly those derived from adeno-associated virus (AAV), for therapeutic delivery of these expression cassettes. This innovation offers novel tools for expressing MeCP2 and holds promise for treating disorders linked to reduced MeCP2 activity.

Career Highlights

Rebekah has worked at esteemed institutions such as the University of Edinburgh and the University of Glasgow. Her research has focused on genetic mechanisms and therapeutic applications, contributing to advancements in the understanding of neurological disorders.

Collaborations

Throughout her career, Rebekah has collaborated with notable scientists, including Adrian Bird and Stuart Robert Cobb. These partnerships have enhanced her research and expanded the impact of her innovations in the field.

Conclusion

Rebekah Tillotson's work in developing MeCP2 expression cassettes represents a significant advancement in genetic therapeutics. Her contributions are vital for the ongoing research and treatment of disorders like Rett syndrome.

This text is generated by artificial intelligence and may not be accurate.
Please report any incorrect information to support@idiyas.com
Loading…