Gorlin syndrome-induced pluripotent stem cells form medulloblastoma with loss of heterozygosity in PTCH1
Y. Ikemoto, T. Miyashita, M. Nasu, H. Hatsuse, K. Kajiwara, K. Fujii, T. Motojima, M. Toyoda, A. UMEZAWA
This study shows that Gorlin syndrome patient-derived iPSCs form medulloblastoma in mice, with one tumor showing PTCH1 loss of heterozygosity.
Aging · May 21, 2020Peer-reviewedCell Biology