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Non-fibro-adipogenic pericytes from human embryonic stem cells attenuate degeneration of the chronically injured mouse muscle. [electronic resource] by
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- Shah, Paras
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- Hu, Vivian J
- McClintick, Daniel J
- Wu, Genbin
- Gatto, Jonathan D
- Xi, Haibin
- Pyle, April D
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- Dar, Ayelet
Producer: 20201015
In:
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Detecting spinal pyramidal tract of amyotrophic lateral sclerosis patients with diffusion tensor tractography. [electronic resource] by
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- Morihara, Ryuta
- Shang, Jingwei
- Takemoto, Mami
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- Yamashita, Toru
- Abe, Koji
Producer: 20181009
In:
Neuroscience research vol. 133
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Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy. [electronic resource] by
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- Hung, Gene
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- Ly, Linda
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- Sopher, Bryce L
- Bennett, C Frank
- Shelton, G Diane
- Cleveland, Don W
- La Spada, Albert R
Producer: 20140605
In:
Neuron vol. 82
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Pioglitazone suppresses neuronal and muscular degeneration caused by polyglutamine-expanded androgen receptors. [electronic resource] by
- Iida, Madoka
- Katsuno, Masahisa
- Nakatsuji, Hideaki
- Adachi, Hiroaki
- Kondo, Naohide
- Miyazaki, Yu
- Tohnai, Genki
- Ikenaka, Kensuke
- Watanabe, Hirohisa
- Yamamoto, Masahiko
- Kishida, Ken
- Sobue, Gen
Producer: 20150923
In:
Human molecular genetics vol. 24
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Peripheral androgen receptor gene suppression rescues disease in mouse models of spinal and bulbar muscular atrophy. [electronic resource] by
- Lieberman, Andrew P
- Yu, Zhigang
- Murray, Sue
- Peralta, Raechel
- Low, Audrey
- Guo, Shuling
- Yu, Xing Xian
- Cortes, Constanza J
- Bennett, C Frank
- Monia, Brett P
- La Spada, Albert R
- Hung, Gene
Producer: 20150105
In:
Cell reports vol. 7
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Tissue-specific somatic mosaicism in spinal and bulbar muscular atrophy is dependent on CAG-repeat length and androgen receptor--gene expression level. [electronic resource] by
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- Reeves, M F
- Ito, Y
- Matsumoto, M
- Li, M
- Miwa, S
- Inukai, A
- Yamamoto, M
- Doyu, M
- Yoshida, M
- Hashizume, Y
- Terao, S
- Mitsuma, T
- Sobue, G
Producer: 20001002
In:
American journal of human genetics vol. 65
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