Houston, TX, United States of America

Jeffrey L Noebels

This inventor holds 1 USPTO granted patent and 1 published patent application. Top assignees: Baylor College of Medicine, The Jackson Laboratory. Active years: 1998.

USPTO Granted Patents = 1 

% Patents Active = 100.0

Average Co-Inventor Count = 4.0

ph-index = 1


Company Filing History:


Years Active: 1998

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1 patent (USPTO):Explore Patents

Title: The Innovations of Jeffrey L. Noebels

Introduction

Jeffrey L. Noebels is a notable inventor based in Houston, TX (US). He has made significant contributions to the field of clinical research, particularly in understanding genetic mutations associated with neurological disorders. His work has implications for diagnosing and treating conditions such as ataxia and epilepsy.

Latest Patents

One of his key patents is an in vitro method for identifying a clinical disorder associated with the Nhe1 gene. This patent discloses the identification of a mutation responsible for ataxia and epilepsy in a murine model system. Specifically, a mutation has been identified within the Nhe1 gene, which results in both ataxia and epilepsy. The specific mutation identified is an A to T transition at nucleotide 1639, which creates a premature stop codon. The identification of this mutation enables methods for the detection of clinical disorders associated with a defect in a cation exchanger, such as Nhe1. He holds 1 patent.

Career Highlights

Throughout his career, Jeffrey has worked with esteemed institutions, including The Jackson Laboratory and Baylor College of Medicine. His research has contributed to advancements in the understanding of genetic disorders and their clinical implications.

Collaborations

Jeffrey has collaborated with notable colleagues, including Cathleen Marie Lutz and Wayne N. Frankel. Their joint efforts have furthered research in the field of genetics and clinical disorders.

Conclusion

Jeffrey L. Noebels is a distinguished inventor whose work has significantly impacted the understanding of genetic mutations related to neurological disorders. His contributions continue to influence the field of clinical research and diagnostics.

Profile summary based on public USPTO records.
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