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...
Main Authors: | 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 |
---|---|
Format: | Online |
Language: | English |
Published: |
Elsevier
2016
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834049/ |
Similar Items
-
Controlling the Regional Identity of hPSC-Derived Neurons to Uncover Neuronal Subtype Specificity of Neurological Disease Phenotypes
by: Imaizumi, Kent, et al.
Published: (2015) -
ALS-FUS pathology revisited: singleton FUS mutations and an unusual case with both a FUS and TARDBP mutation
by: King, Andrew, et al.
Published: (2015) -
ALS-Associated FUS Mutations Result in Compromised FUS Alternative Splicing and Autoregulation
by: Zhou, Yueqin, et al.
Published: (2013) -
Immune activation and MRgFUS
by: Ferrara, Katherine, et al.
Published: (2015) -
Fus Expression Patterns in Developing Tooth
by: Kim, Eun-Jung, et al.
Published: (2013)