Zobrazeno 1 - 10
of 179
pro vyhledávání: '"Takeshi Taketani"'
Publikováno v:
Inflammation and Regeneration, Vol 44, Iss 1, Pp 1-9 (2024)
Abstract The transplantation of human mesenchymal stromal/stem cells (hMSCs) has potential as a curative and permanent therapy for congenital skeletal diseases. However, the self-renewal and differentiation capacities of hMSCs markedly vary. Therefor
Externí odkaz:
https://doaj.org/article/5e17228cd72f4829bb49f02c57a4b432
Autor:
Yuki Kawashima-Sonoyama, Keisuke Wada, Kei Yamamoto, Masanobu Fujimoto, Noriyuki Namba, Takeshi Taketani
Publikováno v:
Endocrine Journal, Vol 71, Iss 7, Pp 687-694 (2024)
Short stature with IGF-1 receptor (IGF1R) gene alteration is known as small-for-gestational-age (SGA) short stature with elevated serum IGF1 levels. Its prevalence and clinical characteristics remain unclear. No adapted treatment is available for sho
Externí odkaz:
https://doaj.org/article/ae4200e683cb4784a31394e6cc26d5e8
Autor:
Aisha Sheriff Kalambe, Kazunobu Sugihara, Kei Yamamoto, Sakiko Kawano, Chigusa Oyama, Takeshi Taketani, Kenji Hayashida, Masaki Tanito
Publikováno v:
Case Reports in Ophthalmology, Vol 14, Iss 1, Pp 477-483 (2023)
PHACE(S) syndrome is a neurocutaneous disorder with a hallmark finding of an infantile facial hemangioma (IFH) >5 cm. Eye examination of patients with PHACE(S) syndrome with no IFH at periorbital region is reported to be of low yield. We report a uni
Externí odkaz:
https://doaj.org/article/94d1b5e0d94f4c958be94ad96495f851
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:
Lu Liu, Jiahao Yang, Yoshinori Otani, Takahiro Shiga, Akihiro Yamaguchi, Yasuaki Oda, Miho Hattori, Tsukimi Goto, Shuichi Ishibashi, Yuki Kawashima-Sonoyama, Takaya Ishihara, Yumi Matsuzaki, Wado Akamatsu, Masashi Fujitani, Takeshi Taketani
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 24, p 17186 (2023)
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode (MELAS) syndrome, caused by a single base substitution in mitochondrial DNA (m.3243A>G), is one of the most common maternally inherited mitochondrial diseases accompanied by ne
Externí odkaz:
https://doaj.org/article/5651d4b992414c9e80ebc8a3ce321ff2
Autor:
Nobuo Kanazawa, Hiroaki Hemmi, Noriko Kinjo, Hidenori Ohnishi, Jun Hamazaki, Hiroyuki Mishima, Akira Kinoshita, Tsunehiro Mizushima, Satoru Hamada, Kazuya Hamada, Norio Kawamoto, Saori Kadowaki, Yoshitaka Honda, Kazushi Izawa, Ryuta Nishikomori, Miyuki Tsumura, Yusuke Yamashita, Shinobu Tamura, Takashi Orimo, Toshiya Ozasa, Takashi Kato, Izumi Sasaki, Yuri Fukuda-Ohta, Naoko Wakaki-Nishiyama, Yutaka Inaba, Kayo Kunimoto, Satoshi Okada, Takeshi Taketani, Koichi Nakanishi, Shigeo Murata, Koh-ichiro Yoshiura, Tsuneyasu Kaisho
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
Genetic variants of proteasome subunit genes have been shown to associate with perturbed immune function. Here authors show that a heterozygous missense variant of the immunoproteasome subunit β-type 9 causes an autoinflammatory/immune deficiency sy
Externí odkaz:
https://doaj.org/article/bc153bd94dab48289d8e89f5cfa52002
Autor:
Kenji Yamada, Yoshimitsu Osawa, Hironori Kobayashi, Ryosuke Bo, Yuichi Mushimoto, Yuki Hasegawa, Seiji Yamaguchi, Takeshi Taketani
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 33, Iss , Pp 100940- (2022)
Multiple acyl-CoA dehydrogenase deficiency (MADD) is an inherited metabolic disease caused by a defect in electron transfer flavoprotein alpha (ETFA), ETF beta (ETFB), or ETF dehydrogenase (ETFDH), and riboflavin metabolism disorders have recently be
Externí odkaz:
https://doaj.org/article/2d52c3790d7b4c34b33e09e155d77d77
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:
Shuntaro Fukushima, Tomoo Takahashi, Kazuki Tsukamoto, Misaki Matsumura, Ryo Takigawa, Yasuo Sakai, Sokichi Maniwa, Lynne Murphy, Takeshi Taketani
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Eye-tracking to evaluate gaze patterns has developed as an assessment tool for children with autism spectrum disorder (ASD). Gazefinder is one of Eye-tracking devices and few studies have investigated whether it can measure the gaze data of
Externí odkaz:
https://doaj.org/article/929b291bb7654f2fbe7b3985752a2cbc
Autor:
Kai Takedani, Masahiro Yamamoto, Sayuri Tanaka, Shinichiro Ishihara, Takeshi Taketani, Keizo Kanasaki
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
In a small number of cases, the development of ectopic residual adrenal lesions during embryogenesis causing Cushing’s syndrome due to the production of excess cortisol has been reported. A 29-year-old woman was admitted to our hospital for fatigue
Externí odkaz:
https://doaj.org/article/a9ec4091cfe545d0a47bde8f30272d01