Kuure lab studies mechanisms of organogenesis with the focus on embryonic kidney and in vivo modeling of rare diseases.

Congenital renal malformations are among the most common birth defects and arise from the failure to normally regulate kidney development. The overall goal of Kuure lab research is to provide new knowledge on the mechanisms underlying kidney development and thus facilitate generation of novel diagnostic and therapeutic interventions for renal diseases.
Read more about our research

Kuure lab on Twitter

@shkuure

Huom! Etsitään organisointitaitoista tiimityöntekijää Oulun yliopistoon monitieteiseen Fibrobesity- hankkeeseen.… twitter.com/i/web/status/1…

Taas pöllytellään etiikan ja turvallisuuden rajoja twitter.com/fingmice/statu…

Happy to present our work on Finnish Disease Mice (FinnDisMice) project here today @SuomenAkatemia @LaaketieteenStwitter.com/i/web/status/1…

@fingmice

Check out the #TT2020 meeting report rdcu.be/cd0Xe to refresh your memories from the October's virtual co… twitter.com/i/web/status/1…

Successful @fingmice webinar so well concluded on Heikki Tanila's last slide - good knowledge of the model AND good… twitter.com/i/web/status/1…

.@fingmice webinar alive! Introduction to the platform by @RHinttala https://t.co/F3kYwG89Al