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Sustained translational repression by eIF2?-P mediates prion neurodegeneration.

• Authors : Moreno, Julie A.; Radford, Helois; Peretti, Diego

Subjects: NEURODEGENERATION; PRIONS; ALZHEIMER'S disease

• Source: Nature. 5/24/2012, Vol. 485 Issue 7399, p507-511. 5p. 4 Graphs.

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Transmissible and genetic prion diseases share a common pathway of neurodegeneration.

• Authors : Hegde, Ramanujan S.; Tremblay, Patrick

Subjects: PRION diseases; NEURODEGENERATION; CELL membranes

• Source: Nature. 12/16/1999, Vol. 402 Issue 6763, p822. 5p. 5 Diagrams, 1 Chart, 13 Graphs.

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PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brain.

• Authors : Blattler, Thomas; Brandner, Sebastian

Subjects: PRIONS; SCRAPIE; SCIENTIFIC experimentation

• Source: Nature. 9/4/1997, Vol. 389 Issue 6646, p69. 5p. 4 Color Photographs, 9 Black and White Photographs, 2 Charts, 1 Graph.

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Modulation of neuronal activity by target uncertainty.

• Authors : Basso, Michele A.; Wurtz, Robert H.

Subjects: SACCADIC eye movements; VISION; PHYSIOLOGY

• Source: Nature. 9/4/1997, Vol. 389 Issue 6646, p66. 4p. 6 Graphs.

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Mammalian prions and their wider relevance in neurodegenerative diseases.

• Authors : Collinge, John

• Source: Nature; 11/10/2016, Vol. 539 Issue 7628, p217-226, 10p, 4 Diagrams

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Normal host prion protein necessary for scrapie-induced neurotoxicity.

• Authors : Brandner S; Department of Pathology, University Hospital, Zürich, Switzerland.; Isenmann S

Subjects: PrPC Proteins/PrPC Proteins/PrPC Proteins/*metabolism ; PrPSc Proteins/PrPSc Proteins/PrPSc Proteins/*toxicity ; Scrapie/Scrapie/Scrapie/*etiology

• Source: Nature [Nature] 1996 Jan 25; Vol. 379 (6563), pp. 339-43.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium:

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