Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Eeva Ventelä"'
Autor:
Kari Vaahtomeri, Tomi P. Mäkelä, Niklas Ekman, Ronald A. DePinho, Eeva Ventelä, Ari Ristimäki, Pekka Katajisto, Robert Feil, Nabeel Bardeesy
Publikováno v:
Nature genetics. 40(4)
Germline mutations in STK11 (also known as LKB1) are found in individuals with Peutz-Jeghers syndrome (PJS) manifesting with gastrointestinal polyps that contain a prominent stromal component. Epithelia in polyps of Stk11(+/-) mice can retain a funct
Autor:
Boris Hinz, Kaisa Laajanen, Kari Vaahtomeri, Tea Vallenius, Marianne Tiainen, Pekka Katajisto, Eeva Ventelä, Pierre-Jean Wipff, Tomi P. Mäkelä
Inactivating mutations of the tumor-suppressor kinase gene LKB1 underlie Peutz-Jeghers syndrome (PJS), which is characterized by gastrointestinal hamartomatous polyps with a prominent smooth-muscle and stromal component. Recently, it was noted that P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcae028b3b4857bc530c093f223440eb
https://infoscience.epfl.ch/record/147732
https://infoscience.epfl.ch/record/147732
Autor:
Pekka Katajisto, Kari Matti Vaahtomeri, Nils Ekman, Eeva Ventelä, Ari Ristimäki, Nabeel Bardeesy, Robert Feil, Ronald DePinho, tomi makela
Publikováno v:
University of Helsinki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::69c31d60c4f2de31de5da65f505bcccd
https://researchportal.helsinki.fi/en/publications/94327544-9757-4510-8739-6db1387c914c
https://researchportal.helsinki.fi/en/publications/94327544-9757-4510-8739-6db1387c914c