Concepedia

SQSTM1 mutations in Han Chinese populations with sporadic amyotrophic lateral sclerosis

Yongping Chen, Zhenzhen Zheng, Xueping Chen, Rui Huang, Yuan Yang, Lixing Yuan, Lei Pan, Shinji Hadano, Huifang Shang

Neurobiology of Aging · 2013 · 58 citations · 10 references

DOI

Concepts

References

10

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

D.R. Rosen, Teepu Siddique, David T. Patterson et al. · Nature · 1993 · 7K citations

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p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death

Geir Bjørkøy, Trond Lamark, Andreas Brech et al. · The Journal of Cell Biology · 2005 · 3.3K citations · Full text

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TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

Jemeen Sreedharan, Ian P. Blair, Vineeta B. Tripathi et al. · Science · 2008 · 2.6K citations · Full text

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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

Edor Kabashi, Paul N. Valdmanis, Patrick A. Dion et al. · Nature Genetics · 2008 · 1.5K citations

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<emph type="ital">SQSTM1</emph> Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

Faisal Fecto · Archives of Neurology · 2011 · 643 citations

, , +15