Prion disease
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Publisher
Elsevier
Reference207 articles.
1. An integrated map of genetic variation from 1,092 human genomes;1000 Genomes Project Consortium;Nature,2012
2. The prion's elusive reason for being;Aguzzi;Annu Rev Neurosci,2008
3. A novel PRNP Y218N mutation in Gerstmann-Straussler-Scheinker disease with neurofibrillary degeneration;Alzualde;J Neuropathol Exp Neurol,2010
4. Crystal structure of human prion protein bound to a therapeutic antibody;Antonyuk;Proc Natl Acad Sci U S A,2009
5. Polymorphism at residue 129 modulates the conformational conversion of the D178N variant of human prion protein;Apetri;Biochemistry,2005
Cited by 27 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. First report of a novel 108 bp deletion and five novel SNPs in PRNP gene of stray cats and in silico analysis of their possible relation with feline spongiform encephalopathy;Topics in Companion Animal Medicine;2024-03
2. Heterogeneity of pathological prion protein accumulation in the brain of moose (Alces alces) from Norway, Sweden and Finland with chronic wasting disease;Veterinary Research;2023-09-08
3. Sleep in Gerstmann-Straüssler-Scheinker disease;Sleep Medicine;2023-08
4. Cardiolipin externalization mediates prion protein (PrP) peptide 106–126-associated mitophagy and mitochondrial dysfunction;Frontiers in Molecular Neuroscience;2023-06-02
5. Enfermedades por priones humanas. Una revisión general;Medicina Clínica;2023-06
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