| | VARIANT: 5621v2 | |
Entry |
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Name |
PRNP oligomeric conformation
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Gene |
PRNP prion protein (Kanno blood group) [KO: K05634]
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Organism |
hsa_var Human gene variants (Homo sapiens)
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Variation |
oligomer |
Network |
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Disease |
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Reference |
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Authors |
Simoneau S, Rezaei H, Sales N, Kaiser-Schulz G, Lefebvre-Roque M, Vidal C, Fournier JG, Comte J, Wopfner F, Grosclaude J, Schatzl H, Lasmezas CI |
Title |
In vitro and in vivo neurotoxicity of prion protein oligomers. |
Journal |
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Reference |
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Authors |
Chiesa R, Piccardo P, Biasini E, Ghetti B, Harris DA |
Title |
Aggregated, wild-type prion protein causes neurological dysfunction and synaptic abnormalities. |
Journal |
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Reference |
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Authors |
Zamponi E, Buratti F, Cataldi G, Caicedo HH, Song Y, Jungbauer LM, LaDu MJ, Bisbal M, Lorenzo A, Ma J, Helguera PR, Morfini GA, Brady ST, Pigino GF |
Title |
Prion protein inhibits fast axonal transport through a mechanism involving casein kinase 2. |
Journal |
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LinkDB |
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