Mika Suga
Nikon
19 Papers
29 Citations
Mika Suga is an academic researcher from Nikon. The author has contributed to research in topics: Induced pluripotent stem cell & Cellular differentiation. The author has an hindex of 9, co-authored 17 publications.
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Papers
Parametric analysis of colony morphology of non-labelled live human pluripotent stem cells for cell quality control.
Ryuji Kato,Megumi Matsumoto,Hiroto Sasaki,Risako Joto,Mai Okada,Yurika Ikeda,Kei Kanie,Mika Suga,Masaki Kinehara,Kana Yanagihara,Yujung Liu,Kozue Uchio-Yamada,Takayuki Fukuda,Hiroaki Kii,Takayuki Uozumi,Hiroyuki Honda,Yasujiro Kiyota,Miho Furue +17 more
TL;DR: The quantitative evaluation method provides a biological definition of ‘hPSC colony morphology’, permits the non-invasive monitoring of hPSC conditions and is particularly useful for detecting variations in hPSCs heterogeneity.
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Bone morphogenetic protein 4 promotes craniofacial neural crest induction from human pluripotent stem cells.
TL;DR: In this article, the authors showed that BMP4-tolerant cranial NC cells were capable of differentiation into osteocytes and chondrocytes from human pluripotent stem cells.
Prediction of Differentiation Tendency Toward Hepatocytes from Gene Expression in Undifferentiated Human Pluripotent Stem Cells
Kana Yanagihara,Yujung Liu,Kei Kanie,Kazuo Takayama,Minako Kokunugi,Mitsuhi Hirata,Takayuki Fukuda,Mika Suga,Hiroki Nikawa,Hiroyuki Mizuguchi,Ryuji Kato,Miho Furue +11 more
TL;DR: A model using gene expression ranking and bioinformatic analysis could reasonably predict poor differentiation propensity of hPSC lines.
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Monitoring of glutamate-induced excitotoxicity by mitochondrial oxygen consumption.
Ayako Kumagai,Tsutomu Sasaki,Kenta Matsuoka,Masayoshi Abe,Toshihide Tabata,Yumi Itoh,Hiroyuki Fuchino,Sartagul Wugangerile,Mika Suga,Tomoko Yamaguchi,Hidehisa Kawahara,Yasuo Nagaoka,Kenji Kawabata,Miho Furue,Hiroshi Takemori +14 more
TL;DR: It was found that pyruvate rather than lactate supported OCR levels and conferred on neurons resistance to glutamate‐mediated excitotoxicity, and astrocytes preferentially used glutamate, not glutamine, for a substrate of the tricarboxylic acid cycle.
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A Simple Method for Labeling Human Embryonic Stem Cells Destined to Lose Undifferentiated Potency
TL;DR: Time‐lapse analyses revealed that JC‐1‐labeled H9 cells under an overconfluent condition were highly differentiated after subculture, suggesting that monitoring oxidative phosphorylation in live cells might facilitate the prediction of induced pluripotent stem cells, as well as ES cells that are destined to lose their undifferentiated potency.
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