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

The 13th ISTT prize winner is Dr. Alexandra Joyner, and her talk will be tomorrow at the #TT2020VIRTUAL meeting....… twitter.com/i/web/status/1…

It is happening now - the first ever virtual transgenic technology meeting #TT2020VIRTUAL is ongoing! Extremely exc… twitter.com/i/web/status/1…

An opportunity to see rodent housing and #CRISPR genome editing experiments @helsinkiuni Finland. #Mousetwitter.com/i/web/status/1…

Keskustelua tärkeästä aiheesta eli siitä miten tutkimuksen merkittävät apulaiset auttavat selvittämään perusbiologi… twitter.com/i/web/status/1…

@fingmice

TV-documentary about the use of genetic engineering and animal models in research broadcasted by the national chann… twitter.com/i/web/status/1…

Dear Colleagues, You are warmly welcome to FinGMice Webinar “Boost your research - national mouse clinic network” M… twitter.com/i/web/status/1…

Excellent talks at helsinki.fi/en/conferences… mtg going on @helsinkiuni @HiLIFE_helsinki #development #StemCells