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pro vyhledávání: '"Takato Mizuta"'
Autor:
Takenobu Katagiri, PhD, Kenji Osawa, Sho Tsukamoto, Mai Fujimoto, Arei Miyamoto, Takato Mizuta
Publikováno v:
Japanese Dental Science Review, Vol 51, Iss 2, Pp 42-50 (2015)
Bone morphogenetic protein (BMP) was originally discovered by Marshall Urist a half century ago following the observation of a unique activity that induced heterotopic bone formation in skeletal muscle tissue. The molecular mechanisms underlying the
Externí odkaz:
https://doaj.org/article/0afb3e0bd4144f74a36848e929fe8d71
Publikováno v:
Japanese Dental Science Review, Vol 51, Iss 2, Pp 42-50 (2015)
Summary Bone morphogenetic protein (BMP) was originally discovered by Marshall Urist a half century ago following the observation of a unique activity that induced heterotopic bone formation in skeletal muscle tissue. The molecular mechanisms underly
Autor:
Takato Mizuta, Takenobu Katagiri, Satoshi Ohte, Shoichiro Kokabu, Naoto Suda, Arei Miyamoto, Mai Fujimoto, Osawa Kenji, Sho Tsukamoto
Publikováno v:
Molecular Endocrinology. 29:140-152
Fibrodysplasia ossificans progressiva (FOP) is a genetic disorder characterized by progressive heterotopic ossification in soft tissues, such as the skeletal muscles. FOP has been shown to be caused by gain-of-function mutations in activin receptor-l
Autor:
Sho Tsukamoto, Shoichiro Kokabu, Katsumi Yoneyama, E. Murata, Osawa Kenji, Takato Mizuta, Eijiro Jimi, Mai Fujimoto, Takenobu Katagiri, Satoshi Ohte, Arei Miyamoto, Aiko Machiya
Publikováno v:
Scientific Reports
Smad1, Smad5 and Smad9 (also known as Smad8) are activated by phosphorylation by bone morphogenetic protein (BMP)-bound type I receptor kinases. We examined the role of Smad1, Smad5, and Smad9 by creating constitutively active forms (Smad(DVD)). Tran
Autor:
Katsumi Yoneyama, Masashi Shin, Shoichiro Kokabu, Osawa Kenji, Satoshi Ohte, Akihiko Okuda, Naoto Suda, Takato Mizuta, Sho Tsukamoto, Mai Fujimoto, Aiko Machiya, Takenobu Katagiri, Arei Miyamoto
Publikováno v:
Biochemical and biophysical research communications. 455(3-4)
Fibrodysplasia ossificans progressiva (FOP) is a genetic disorder characterized by heterotopic endochondral ossification in soft tissue. A mutation in the bone morphogenetic protein (BMP) receptor ALK2, R206H, has been identified in patients with typ