Helsingin Yliopisto, Finland

Päivi Peltomäki

USPTO Granted Patents = 1 

 

Average Co-Inventor Count = 3.0

ph-index = 1


Company Filing History:


Years Active: 2018

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1 patent (USPTO):Explore Patents

Title: Päivi Peltomäki: Innovator in DNA Mismatch Repair Function

Introduction

Päivi Peltomäki is a distinguished inventor based at Helsingin Yliopisto in Finland. He has made significant contributions to the field of genetics, particularly in the area of DNA mismatch repair. His innovative work has implications for diagnostics and understanding genetic disorders.

Latest Patents

Päivi Peltomäki holds a patent for a method to determine DNA mismatch repair function. This invention relates to a quantitative method for assessing whether a human subject has an impaired DNA mismatch repair function. The process involves providing a diagnostic sample from the human subject and producing a nuclear extract from that sample. It includes the use of MMR proficient and MMR deficient nuclear extracts as controls, combining these with mismatch bearing substrate DNA molecules, and performing a mismatch repair assay. The method ultimately determines the capability of the sample nuclear extract to repair the substrate DNA molecule. The invention also encompasses a kit that provides the necessary reagents for use in this method. He has 1 patent to his name.

Career Highlights

Päivi Peltomäki has dedicated his career to advancing the understanding of genetic repair mechanisms. His work at Helsingin Yliopisto has positioned him as a key figure in genetic research, contributing to both academic knowledge and practical applications in diagnostics.

Collaborations

Päivi has collaborated with notable colleagues, including Minna Nyström and Minttu Kansikas, to further enhance the impact of his research and innovations.

Conclusion

Päivi Peltomäki's contributions to the field of DNA mismatch repair function highlight his role as an important inventor in genetic research. His innovative methods and collaborative efforts continue to advance the understanding of genetic disorders and diagnostics.

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