Helsingin Yliopisto, Finland

Minttu Kansikas



 

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: Minttu Kansikas: Innovator in DNA Mismatch Repair Function

Introduction

Minttu Kansikas is a notable inventor based at Helsingin Yliopisto in Finland. She has made significant contributions to the field of genetics, particularly in the area of DNA mismatch repair. Her innovative work has the potential to enhance diagnostic methods for various genetic disorders.

Latest Patents

Minttu Kansikas 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 at least one mismatch bearing substrate DNA molecule, and performing a mismatch repair assay. The method aims to determine if the sample nuclear extract can repair the substrate DNA molecule, utilizing normal, non-malignant constitutive cells such as fibroblasts. Additionally, the invention encompasses a kit that provides the necessary reagents for use in this method.

Career Highlights

Minttu Kansikas has dedicated her career to advancing the understanding of DNA repair mechanisms. Her work at Helsingin Yliopisto has positioned her as a key figure in genetic research. With her innovative approach, she has contributed to the development of diagnostic tools that can aid in the identification of genetic disorders.

Collaborations

Minttu collaborates with esteemed colleagues such as Minna Nyström and Päivi Peltomäki. These partnerships enhance the research environment and foster innovation in the field of genetics.

Conclusion

Minttu Kansikas is a pioneering inventor whose work in DNA mismatch repair function is making a significant impact in genetic diagnostics. Her contributions are vital for advancing our understanding of genetic disorders and improving diagnostic methods.

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