Image 3_Investigation of early axonal phenotypes in an iPSC-derived ALS cellular model using a microfluidic device.tif

Introduction<p>Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease caused by the loss of upper and lower motor neurons. Mutations in the FUS/TLS gene have been reported as the second most common mutation in Japanese patients with familial ALS. In recent years, lower...

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Библиографические подробности
Главный автор:	Asako Otomo (251531) (author)
Другие авторы:	Keiko Nishijima (21776255) (author), Yuta Murakami (2178398) (author), Mitsuru Ishikawa (606461) (author), Haruka Yudahira (21776258) (author), Kento Shimakura (21776261) (author), Hideyuki Okano (47690) (author), Masashi Aoki (35088) (author), Hiroshi Kimura (3849) (author), Shinji Hadano (251529) (author)
Опубликовано:	2025
Предметы:	Cellular Interactions (incl. Adhesion, Matrix, Cell Wall) amyotrophic lateral sclerosis (ALS) iPSCs microfluidic device FUS/TLS lower motor neurons
Метки:	Добавить метку Нет меток, Требуется 1-ая метка записи!

Image 3_Investigation of early axonal phenotypes in an iPSC-derived ALS cellular model using a microfluidic device.tif

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