The role of eutherian‐specific RTL1 in the nervous system and its implications for the Kagami‐Ogata and Temple syndromes

av Kitazawa, Moe, Sutani, Akito, Kaneko‐Ishino, Tomoko, Ishino, Fumitoshi
I publikationen Genes Cells (2021)

Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes

av Kitazawa, Moe, Hayashi, Shinichiro, Imamura, Michihiro, Takeda, Shin'ichi, Oishi, Yumiko, Kaneko-Ishino, Tomoko, Ishino, Fumitoshi
I publikationen Development (2020)

Double strand break repair by capture of retrotransposon sequences and reverse-transcribed spliced mRNA sequences in mouse zygotes

av Ono, Ryuichi, Ishii, Masayuki, Fujihara, Yoshitaka, Kitazawa, Moe, Usami, Takako, Kaneko-Ishino, Tomoko, Kanno, Jun, Ikawa, Masahito, Ishino, Fumitoshi
I publikationen Sci Rep (2015)

A trans-homologue interaction between reciprocally imprinted miR-127 and Rtl1 regulates placenta development

av Ito, Mitsuteru, Sferruzzi-Perri, Amanda N., Edwards, Carol A., Adalsteinsson, Bjorn T., Allen, Sarah E., Loo, Tsui-Han, Kitazawa, Moe, Kaneko-Ishino, Tomoko, Ishino, Fumitoshi, Stewart, Colin L., Ferguson-Smith, Anne C.
I publikationen Development (2015)