| Citations for Anti SALL1 (Mouse) – 10 Found |
| Mellissa C Alcantara, Kentaro Suzuki, Alvin R Acebedo, Daiki Kajioka, Satoshi Hirohata, Tsuneyasu Kaisho, Yu Hatano, Kazuo Yamagata, Satoru Takahashi, Gen Yamada. Androgen-regulated MafB drives cell migration via MMP11-dependent extracellular matrix remodeling in mice. iScience. 2022;25(12):105609. PubMed |
| Hiraku Tsujimoto, Tomoko Kasahara, Shin-ichi Sueta, Makoto Ikeya, Akira Watanabe, Kenji Osafune. A Modular Differentiation System Maps Multiple
Human Kidney Lineages from Pluripotent Stem Cells. Cell Reports. 2020;31:107476. |
| Hitomi Matsunari, Masahito Watanabe, Koki Hasegawa, Ayuko Uchikura, Kazuaki Nakano, Kazuhiro Umeyama, Hideki Masaki, Sanae Hamanaka, Tomoyuki Yamaguchi, Masaki Nagaya, Ryuichi Nishinakamura, Hiromitsu Nakauchi, and Hiroshi Nagashima. Compensation of Disabled Organogeneses in Genetically Modified Pig
Fetuses by Blastocyst Complementation. Stem Cell Reports. 2020;14:21-33. |
| Alvin R. Acebedo, Kentaro Suzuki, Shinjiro Hino, Mellissa C. Alcantara, Yuki Sato, Hisashi Haga, Ken-ichi Matsumoto, Mitsuyoshi Nakao, Kenji Shimamura, Toru Takeo, Naomi Nakagata, Shinichi Miyagawa, Ryuichi Nishinakamura, Robert S. Adelstein & Gen Yamada. Mesenchymal actomyosin contractility is required for androgen-driven urethral masculinization in mice. Communications Biology volume. 2019; |
| Reconstitution of the embryonic kidney identifies a donor cell contribution to the renal vasculature upon transplantation. Reconstitution of the embryonic kidney identifies a donor cell contribution to the renal vasculature upon transplantation. Scientific Reports. 2019;1172 |
| Yusuke Kaku, Atsuhiro Taguchi, Shunsuke Tanigawa, Fahim Haque, Tetsushi Sakuma, Takashi Yamamoto & Ryuichi Nishinakamura. PAX2 is dispensable for in vitro nephron formation from human induced pluripotent stem cells. Scientific Reports . 2017;4554 |
| Tomoko Ohmori, Shunsuke Tanigawa, Yusuke Kaku, Sayoko Fujimura & Ryuichi Nishinakamura . Sall1 in renal stromal progenitors non-cell autonomously restricts the excessive expansion of nephron progenitors. Scientific Reports . 2015;15676 |
Masayo Sakaki-Yumoto, Chiyoko Kobayashi, Akira Sato, Sayoko Fujimura, Yuko Matsumoto, Minoru Takasato, Tatsuhiko Kodama, Hiroyuki Aburatani, Makoto Asashima, Nobuaki Yoshida, Ryuichi Nishinakamura. The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development. DEVELOPMENT AND DISEASE. 2006;133(15):3005-3013.
- Comments: Keywords:Sall4, spalt, Embryonic stem cells, Okihiro syndrome, Townes-Brocks syndrome, Organogenesis, Mouse |
| Akira Sato, Shosei Kishida, Toshiya Tanaka, Akira Kikuchi, Tatsuhiko Kodama, Makoto Asashima, Ryuichi Nishinakamura. Sall1, a causative gene for Townes–Brocks syndrome, enhances the canonical Wnt signaling by localizing to heterochromatin. Biochemical and Biophysical Research Communications. 2004;319(1):103-113. |
| Ryuichi Nishinakamura, Yuko Matsumoto, Kazuki Nakao, Kenji Nakamura, Akira Sato, Neal G. Copeland, Debra J. Gilbert, Nancy A. Jenkins, Sheila Scully, David L. Lacey, Motoya Katsuki, Makoto Asashima, Takashi Yokota. Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development. Development . 2001;128(16):3105-3115. |
