Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells

Amyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disorder. Although its neuropathology is well understood, the cellular and molecular mechanisms are yet to be elucidated due to limitations in the currently available human genetic data. In this study, we generated induced pluripotent...

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Detalles Bibliográficos
Autores principales: Ichiyanagi, Naoki, Fujimori, Koki, Yano, Masato, Ishihara-Fujisaki, Chikako, Sone, Takefumi, Akiyama, Tetsuya, Okada, Yohei, Akamatsu, Wado, Matsumoto, Takuya, Ishikawa, Mitsuru, Nishimoto, Yoshinori, Ishihara, Yasuharu, Sakuma, Tetsushi, Yamamoto, Takashi, Tsuiji, Hitomi, Suzuki, Naoki, Warita, Hitoshi, Aoki, Masashi, Okano, Hideyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834049/
https://www.ncbi.nlm.nih.gov/pubmed/26997647
http://dx.doi.org/10.1016/j.stemcr.2016.02.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834049/
https://www.ncbi.nlm.nih.gov/pubmed/26997647
http://dx.doi.org/10.1016/j.stemcr.2016.02.011

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