Berlin, Germany

Klaus Giese

USPTO Granted Patents = 27 

 

 

Average Co-Inventor Count = 2.7

ph-index = 10

Forward Citations = 594(Granted Patents)


Location History:

  • Castro Valley, CA (US) (1998)
  • San Francisco, CA (US) (2003 - 2010)
  • Berlin, DE (2002 - 2023)

Company Filing History:


Years Active: 1998-2023

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27 patents (USPTO):Explore Patents

Title: Klaus Giese: Innovator in RNA Technology

Introduction: Klaus Giese, based in Berlin, Germany, is an accomplished inventor specializing in the field of ribonucleic acid (RNA) technology. With a remarkable portfolio of 27 patents, Giese has significantly contributed to the scientific community through his innovative ideas and inventions.

Latest Patents: Among his notable patents, Giese has developed interfering RNA molecules, which consist of a double-stranded structure. This innovation includes a first strand that is partially complementary to a target nucleic acid and a second strand that is partially identical to a target nucleic acid, with the double-stranded structure being blunt-ended. This invention showcases Giese's expertise in manipulating RNA for potential therapeutic applications.

Career Highlights: Throughout his career, Klaus Giese has worked with prominent companies such as Silence Therapeutics GmbH and Silence Therapeutics Aktiengesellschaft. These roles have allowed him to advance his research and bring his patented inventions to fruition within the biotech industry.

Collaborations: Giese has also collaborated with several prominent professionals in his field, including Jörg Kaufmann and Anke Klippel-Giese. These collaborations have likely enhanced his innovative capabilities and facilitated the development of groundbreaking RNA technologies.

Conclusion: Klaus Giese stands out as a key figure in RNA research and innovation. His extensive patent portfolio reflects his commitment to advancing scientific understanding and technology. As he continues to push the boundaries of RNA technology, Giese's contributions will undoubtedly shape the future of genetic research and therapeutic development.

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