Zobrazeno 1 - 10
of 2 594
pro vyhledávání: '"Tomatsu A"'
Autor:
Yasumasa Yoshino, Tomoka Hasegawa, Shukei Sugita, Eisuke Tomatsu, Naoya Murao, Izumi Hiratsuka, Sahoko Sekiguchi-Ueda, Megumi Shibata, Takeo Matsumoto, Norio Amizuka, Yusuke Seino, Takeshi Takayanagi, Yoshihisa Sugimura, Atsushi Suzuki
Publikováno v:
Fujita Medical Journal, Vol 10, Iss 4, Pp 87-93 (2024)
Objectives: Phosphate (Pi) induces differentiation of arterial smooth muscle cells to the osteoblastic phenotype by inducing the type III Na-dependent Pi transporter Pit-1/solute carrier family member 1. This induction can contribute to arterial calc
Externí odkaz:
https://doaj.org/article/d63d1cf08fb8404db202eb3f2f20bc9f
Autor:
Estera Rintz, Betul Celik, Nidhi Fnu, Angélica María Herreño-Pachón, Shaukat Khan, Eliana Benincore-Flórez, Shunji Tomatsu
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 35, Iss 2, Pp 102211- (2024)
Mucopolysaccharidosis type IVA (MPS IVA) is caused by a deficiency of the galactosamine (N-acetyl)-6-sulfatase (GALNS) enzyme responsible for the degradation of specific glycosaminoglycans (GAGs). The progressive accumulation of GAGs leads to various
Externí odkaz:
https://doaj.org/article/2f3e9aa130624ddab430b233b94c89ae
Autor:
Luisa N. Pimentel-Vera, Alexander Rodríguez-López, Angela J. Espejo-Mojica, Aura María Ramírez, Carolina Cardona, Luis H. Reyes, Shunji Tomatsu, Thapakorn Jaroentomeechai, Matthew P. DeLisa, Oscar F. Sánchez, Carlos J. Alméciga-Díaz
Publikováno v:
Heliyon, Vol 10, Iss 12, Pp e32555- (2024)
Mucopolysaccharidosis IVA (MPS IVA) is a lysosomal storage disease caused by mutations in the gene encoding the lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS), resulting in the accumulation of keratan sulfate (KS) and chondroitin-
Externí odkaz:
https://doaj.org/article/c416a701f4074f4abb9006fd40dbe25c
Autor:
Pimentel-Vera, Luisa N., Rodríguez-López, Alexander, Espejo-Mojica, Angela J., Ramírez, Aura María, Cardona, Carolina, Reyes, Luis H., Tomatsu, Shunji, Jaroentomeechai, Thapakorn, DeLisa, Matthew P., Sánchez, Oscar F., Alméciga-Díaz, Carlos J.
Publikováno v:
In Heliyon 30 June 2024 10(12)
Autor:
Rintz, Estera, Celik, Betul, Fnu, Nidhi, Herreño-Pachón, Angélica María, Khan, Shaukat, Benincore-Flórez, Eliana, Tomatsu, Shunji
Publikováno v:
In Molecular Therapy - Nucleic Acids 11 June 2024 35(2)
Autor:
Muraki, Nao, Kawabe, Nozomi, Ohashi, Ayano, Umeda, Kanna, Katsuda, Masahito, Tomatsu, Aya, Yoshida, Mikina, Komeda, Kazuki, Minna, John D., Tanaka, Ichidai, Morise, Masahiro, Matsushima, Miyoko, Matsui, Yusuke, Kawabe, Tsutomu, Sato, Mitsuo
Publikováno v:
In Experimental Cell Research 1 June 2024 439(1)
Publikováno v:
Journal of the American College of Emergency Physicians Open, Vol 5, Iss 2, Pp n/a-n/a (2024)
Externí odkaz:
https://doaj.org/article/734efb92d563465484b4df24978ecfe4
Autor:
Aoi, Shinya, Tomatsu, Ryoe, Yabuuchi, Yuki, Morozumi, Daiki, Okamoto, Kota, Fujiki, Soichiro, Senda, Kei, Tsuchiya, Kazuo
Legged robots have excellent terrestrial mobility for traversing diverse environments and thus have the potential to be deployed in a wide variety of scenarios. However, they are susceptible to falling and leg malfunction during locomotion. Although
Externí odkaz:
http://arxiv.org/abs/2107.01837
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Our rich behavioural repertoire is supported by complicated synaptic connectivity in the central nervous system, which must be modulated to prevent behavioural control from being overwhelmed. For this modulation, presynaptic inhibition is an
Externí odkaz:
https://doaj.org/article/697ab210e78746549eaa94a7c5cc6a86
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 15, p 8339 (2024)
Bone development is characterized by complex regulation mechanisms, including signal transduction and transcription factor-related pathways, glycobiological processes, cellular interactions, transportation mechanisms, and, importantly, chemical forma
Externí odkaz:
https://doaj.org/article/e75c645339c046a593a2095719717aa2