Ellicott City, MD, United States of America

P Paul Liu

This inventor holds 1 USPTO granted patent. Top assignee: Other. Active years: 2003.


% Patents Active = 100.0

Average Co-Inventor Count = 14.0

ph-index = 1


Company Filing History:

goldMedal1 out of 834,411 
Other
 patents

Years Active: 2003

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1 patent (USPTO):Explore Patents

Title: The Innovations of P Paul Liu

Introduction

P Paul Liu is a notable inventor based in Ellicott City, MD (US). He has made significant contributions to the field of genetics, particularly in relation to familial Mediterranean fever (FMF). His work has led to advancements in understanding the genetic basis of this condition.

Latest Patents

Liu holds a patent for the invention titled "Pyrin gene and mutants thereof, which cause familial Mediterranean fever." This invention provides the nucleic acid sequence encoding the protein associated with FMF, designated as MEFV. It also includes fragments of the DNA sequence, the corresponding RNA transcript, and the amino acid sequence for the pyrin protein. Notably, the invention discloses three missense mutations clustered within the highly conserved rfp (B30.2) domain at the C-terminal of the protein. These mutants include M6801, M694V, K695R, and V726A. Additionally, the invention encompasses methods for diagnosing patients at risk for FMF and the development of diagnostic kits.

Career Highlights

Throughout his career, Liu has focused on genetic research and the implications of his findings for medical science. His patent reflects a deep understanding of molecular biology and its applications in diagnosing genetic disorders.

Collaborations

Liu has collaborated with esteemed colleagues, including Daniel L Kastner and Ivona Aksentijevich. These partnerships have likely enhanced the depth and impact of his research.

Conclusion

P Paul Liu's contributions to the field of genetics, particularly through his patent related to familial Mediterranean fever, highlight his role as an influential inventor. His work continues to pave the way for advancements in genetic diagnostics and understanding of hereditary conditions.

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