Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mako Ago"'
Autor:
Jiahao Yang, Lu Liu, Yasuaki Oda, Keisuke Wada, Mako Ago, Shinichiro Matsuda, Miho Hattori, Tsukimi Goto, Yuki Kawashima, Yumi Matsuzaki, Takeshi Taketani
Publikováno v:
Stem Cell Research & Therapy, Vol 14, Iss 1, Pp 1-22 (2023)
Abstract Background Mitochondrial dysfunction caused by mutations in mitochondrial DNA (mtDNA) or nuclear DNA, which codes for mitochondrial components, are known to be associated with various genetic and congenital disorders. These mitochondrial dis
Externí odkaz:
https://doaj.org/article/04f5c029444e4985a8703536031f60cd
Autor:
Jiahao Yang, Lu Liu, Yasuaki Oda, Keisuke Wada, Mako Ago, Shinichiro Matsuda, Miho Hattori, Tsukimi Goto, Shuichi Ishibashi, Yuki Kawashima-Sonoyama, Yumi Matsuzaki, Takeshi Taketani
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 12, p 10294 (2023)
Mitochondria are essential organelles for maintaining intracellular homeostasis. Their dysfunction can directly or indirectly affect cell functioning and is linked to multiple diseases. Donation of exogenous mitochondria is potentially a viable thera
Externí odkaz:
https://doaj.org/article/3db0c0e9244b4a37b32a79faa0295908
Autor:
Shuichi Ishibashi, Yoshitsugu Tajima, Soichi Nakada, Yoko Ota, Jyunko Manako, Mako Ago, Naoaki Shibata, Takeshi Taketani, Koji Kumori
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 32, Iss , Pp 1-4 (2018)
We report a case of a neonate with Altman typeⅠsacrococcygeal teratoma (SCT) with spinal canal involvement, in which ultrasonography was useful in the evaluation of the tumor progression into the spinal canal. The male fetus was diagnosed with Altm
Externí odkaz:
https://doaj.org/article/b4f0693a68404efb844d7cf00ff0e445
Autor:
Kenji Yamada, Ryosuke Bo, Hironori Kobayashi, Yuki Hasegawa, Mako Ago, Seiji Fukuda, Seiji Yamaguchi, Takeshi Taketani
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 59-61 (2017)
Carnitine palmitoyltransferase II (CPT-2) deficiency, an autosomal recessive disorder of fatty acid oxidation, can be detected by newborn screening using tandem mass spectrometry (TMS). Our case was a boy born at 38 weeks and 6 days of gestation via
Externí odkaz:
https://doaj.org/article/870d418671b84b1aaf252478f10d66c9
Publikováno v:
American Journal of Perinatology Reports, Vol 07, Iss 01, Pp e1-e4 (2017)
Abstract Background Pial arteriovenous fistula (AVF) is composed of one or more direct arterial feeding vessels with a single draining vein without nidus. A patient with the disease with high-flow AV shunting in the neonatal period not only suffers
Externí odkaz:
https://doaj.org/article/e718653a4ffa47868e0b675213b643d1
Autor:
Taketani, Jiahao Yang, Lu Liu, Yasuaki Oda, Keisuke Wada, Mako Ago, Shinichiro Matsuda, Miho Hattori, Tsukimi Goto, Shuichi Ishibashi, Yuki Kawashima-Sonoyama, Yumi Matsuzaki, Takeshi
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 12; Pages: 10294
Mitochondria are essential organelles for maintaining intracellular homeostasis. Their dysfunction can directly or indirectly affect cell functioning and is linked to multiple diseases. Donation of exogenous mitochondria is potentially a viable thera
Autor:
Takeshi Taketani, Koji Kumori, Mako Ago, Yoshitsugu Tajima, Soichi Nakada, Shuichi Ishibashi, Jyunko Manako, Naoaki Shibata, Yoko Ota
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 32, Iss, Pp 1-4 (2018)
We report a case of a neonate with Altman typeⅠsacrococcygeal teratoma (SCT) with spinal canal involvement, in which ultrasonography was useful in the evaluation of the tumor progression into the spinal canal. The male fetus was diagnosed with Altm
Publikováno v:
AJP Reports
American Journal of Perinatology Reports, Vol 07, Iss 01, Pp e1-e4 (2017)
American Journal of Perinatology Reports, Vol 07, Iss 01, Pp e1-e4 (2017)
Background Pial arteriovenous fistula (AVF) is composed of one or more direct arterial feeding vessels with a single draining vein without nidus. A patient with the disease with high-flow AV shunting in the neonatal period not only suffers from high-
Autor:
Maki Fukami, Etsuko Hirose, Mako Ago, Tsutomu Ogata, Kaori Maruwaka, Hiroyuki Ono, Akira Ohishi, Yuki Uchida, Fumiko Kato, Gen Nishimura, Hiroshi Suzumura
Publikováno v:
American Journal of Medical Genetics Part A. 173:157-162
Syndromic craniosynostoses usually occur as single gene disorders. In this study, we analyzed FGFR1-3 genes in four patients with Crouzon syndrome (CS), four patients with Pfeiffer syndrome type 2 (PS-2), one patient with Jackson-Weiss syndrome (JWS)
Autor:
Mako Ago, Takeshi Taketani, Kenji Yamada, Hironori Kobayashi, Ryosuke Bo, Seiji Yamaguchi, Yuki Hasegawa, Seiji Fukuda
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 59-61 (2017)
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 59-61 (2017)
Carnitine palmitoyltransferase II (CPT-2) deficiency, an autosomal recessive disorder of fatty acid oxidation, can be detected by newborn screening using tandem mass spectrometry (TMS). Our case was a boy born at 38 weeks and 6 days of gestation via