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注意:仅列出部分参考文献,下载原文获取全部文献信息。Human stem cell models of neurodegeneration: From basic science of amyotrophic lateral sclerosis to clinical translation
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Ryoichi Nakamura et al.
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Joseph R. Klim et al.
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Ze'ev Melamed et al.
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Yingxiao Shi et al.
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Taru Tukiainen et al.
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Adriano Chio et al.
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Gabriel E. Hoffman et al.
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Hazuki Watanabe et al.
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Samuel Sances et al.
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Early and gender-specific differences in spinal cord mitochondrial function and oxidative stress markers in a mouse model of ALS
Daniel Cacabelos et al.
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Mercedes Prudencio et al.
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Eun Ah Chang et al.
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Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion
Adrian J. Waite et al.
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Keisuke Okita et al.
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Stefan K. Schulze et al.
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Aritoshi Iida et al.
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Keisuke Okita et al.
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The sex ratio in amyotrophic lateral sclerosis: A population based study
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Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients
Christiaan G. J. Saris et al.
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Junying Yu et al.
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Sexual dimorphism in disease onset and progression of a rat model of ALS
Masatoshi Suzuki et al.
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Differential expression of genes in amyotrophic lateral sclerosis revealed by profiling the post mortem cortex
Xin-Sheng Wang et al.
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Gender-specific gene expression in post-mortem human brain: Localization to sex chromosomes
MP Vawter et al.
NEUROPSYCHOPHARMACOLOGY (2004)