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J. Paul Taylor et al.
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Melanie Lalancette-Hebert et al.
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Ross A. Jones et al.
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Renzo Mancuso et al.
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Xueping Chen et al.
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Martin R. Turner et al.
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Bradley J. Turner et al.
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Joseph W. Lewcock et al.
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Y Furukawa et al.
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H Kikuchi et al.
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PA Jonsson et al.
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M Vorgerd et al.
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F Achilli et al.
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C Hetz et al.
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LR Fischer et al.
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GM Alexander et al.
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J Wang et al.
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Association of the chaperone (GRP58/ER-60/ERp57) with membrane glucose-regulated protein 58 stat3 in cytosol and plasma complexes
GG Guo et al.
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Subcellular distribution of superoxide dismutases (SOD) in rat liver - Cu,Zn-SOD in mitochondria
A Okado-Matsumoto et al.
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Formation of high molecular weight complexes of mutant Cu,Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis
JA Johnston et al.
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