Selective depletion of AMH-expressing granulosa cells in vivo impairs follicular development and fertility in female mice
Tsutomu Endo, Mayu Tamemasa, Kana Hayakawa…·Masami Kanai‐Azuma
Author
Tokyo Medical and Dental UniversityORCID 0000-0002-7782-445XUnclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
8 papers
Recent·Most cited
Tsutomu Endo, Mayu Tamemasa, Kana Hayakawa…·Masami Kanai‐Azuma
Han Xiao, Aya Uchida, Seohyeon Lee…·Yoshiakira Kanai
This study shows that ectopic SOX17 in Sertoli cells promotes Sertoli valve formation and partially rescues infertility in Sox17-null mice.
Yoshifumi Fujioka, Hirosuke Shiura, Masayuki Ishii…·Fumitoshi Ishino
This study shows that knocking out Rtl8a and Rtl8b in mice leads to reduced social behavior, increased apathy, and obesity, likely due to decreased GABRB2 expression in the brain.
Yoshifumi Fujioka, Hirosuke Shiura, Masayuki Ishii…·Fumitoshi Ishino
This study shows that Rtl8a and Rtl8b double knockout mice develop late-onset obesity and neurodevelopmental defects, indicating these retrovirus-derived genes are important for brain function.
Gerel Melig, Ikuo Nobuhisa, Kiyoka Saito…·Tetsuya Taga
This study identifies Rasip1 as a downstream target of Sox17 that enhances hematopoietic activity in intra-aortic hematopoietic clusters of midgestation mouse embryos.
Okiko Habara, Catriona Y. Logan, Masami Kanai‐Azuma…·Hinako M. Takase
This study shows that Wnt signaling in pre-granulosa cells is essential for follicle activation and oocyte maturation, with a two-step model involving self-activation of Wnt and subsequent support of oocyte reawakening.
Rie Saba, Keiko Kitajima, Lucille Rainbow…·Kenta Yashiro
This study shows that Sox17 expression in cardiac progenitor cells biases their fate toward the endocardium and regulates myocardium development through NOTCH signaling in mice.
Risa Nomura, Kenichi Kashimada, Hitomi Suzuki…·Tomohiro Morio
This paper shows that Nr5a1 suppression during fetal development optimizes ovarian development by fine-tuning Notch signaling, using mouse models with altered Nr5a1 expression.