Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Aiko Machiya"'
Autor:
Shigeru Watanabe, Yukiko Yamamura, Aiko Hoshiai, Shiho Morishita, Aiko Machiya, Satoru Matsuda, Takahiro Shimojima, Iwai Tohnai
Publikováno v:
Dental, Oral and Maxillofacial Research. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c68dc6558997484cf597144f64ccb055
https://doi.org/10.15761/domr.1000377
https://doi.org/10.15761/domr.1000377
Publikováno v:
Bone. 137:115456
Teeth consist of two major tissues, enamel and dentin, which are formed during development by epithelial and mesenchymal cells, respectively. Rodent incisors are useful experimental models for studying the molecular mechanisms of tooth formation beca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f144a97707b5b7160493f28a19ff1e33
https://doi.org/10.1016/j.bone.2020.115456
https://doi.org/10.1016/j.bone.2020.115456
Autor:
Alex N. Bullock, Aiko Machiya, Naoto Suda, Mai Fujimoto, Kumagai Keigo, Satoshi Ohte, Sho Tsukamoto, Mai Kuratani, Osawa Kenji, Takenobu Katagiri
Publikováno v:
Bone. 111
Various substitution mutations in ALK2, a transmembrane serine/threonine kinase receptor for bone morphogenetic proteins (BMPs), have been identified in patients with genetic disorders such as fibrodysplasia ossificans progressiva (FOP), diffuse intr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edf673d83b70d65642f88329cfa0a338
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c39e3a6f221a4cfac4ddb1dfa5a15433
https://doi.org/10.1038/srep07596
https://doi.org/10.1038/srep07596
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e31684cf92390926758668380de3c2f4
https://pubmed.ncbi.nlm.nih.gov/25446088
https://pubmed.ncbi.nlm.nih.gov/25446088