Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity

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Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity

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bilimsel makale

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scientific article published on 06 September 2016

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Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity

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Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity.

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Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity

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Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity.

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Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity

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Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity.

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P1476

Bivalent Copper Ions Promote Fibrillar Aggregation of KCTD1 and Induce Cytotoxicity

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P2093

Deyin Guo

http://www.w3.org/2001/XMLSchema#string

Feifei Song

http://www.w3.org/2001/XMLSchema#string

Guihong Sun

http://www.w3.org/2001/XMLSchema#string

Jingwen Wang

http://www.w3.org/2001/XMLSchema#string

Qiushuang Xiong

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Zhepeng Liu

http://www.w3.org/2001/XMLSchema#string

Zhi-Li Ma

http://www.w3.org/2001/XMLSchema#string

P2860

KCTD5, a putative substrate adaptor for cullin3 ubiquitin ligases

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PrPC interacts with potassium channel tetramerization domain containing 1 (KCTD1) protein through the PrP(51-136) region containing octapeptide repeats.

Characterization and expression of a human KCTD1 gene containing the BTB domain, which mediates transcriptional repression and homomeric interactions.

The cellular prion protein binds copper in vivo.

KCTD1 suppresses canonical Wnt signaling pathway by enhancing β-catenin degradation.

The ubiquitin proteasome system in neurodegenerative diseases: sometimes the chicken, sometimes the egg.

The ubiquitin-proteasome pathway in Parkinson's disease and other neurodegenerative diseases.

Metals in neurobiology: probing their chemistry and biology with molecular imaging.

P2888

srep32658

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32658

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P31

scholarly article

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10.1038/SREP32658

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P407

English

P478

http://www.w3.org/2001/XMLSchema#string

P577

2016-09-06T00:00:00Z

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P6179

1047951078

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P698

27596723

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P921

cytotoxicity

P932

5011690

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