Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein

By Wadsworth Jonathan D. F.   Joiner Susan   Linehan Jacqueline M.   Cooper Sharon   Powell Caroline   Mallinson Gary   Buckell Jennifer   Gowland Ian   Asante Emmanuel A.   Budka Herbert   Brandner Sebastian   Collinge John  

Brain, Vol. 129, Iss. 6, 2006-06 ,pp. : 1557-1569

Oxford University Press

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Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein gene

By Varges Daniela   Schulz-Schaeffer Walter   Wemheuer Wiebke   Damman Insa   Schmitz Matthias   Cramm Maria   Kallenberg Kai   Shirneshan Katayoon   Elkenani Manar   Markwort Susanne   Faist Michael   Kohlhase Jürgen   Windl Otto   Zerr Inga  

Journal of Neurology, Vol. 260, Iss. 7, 2013-07 ,pp. : 1871-1879

Springer Publishing Company

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Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breeds

By Sander Petra   Hamann Henning   Pfeiffer Ina   Wemheuer Wilhelm   Brenig Bertram   Groschup Martin   Ziegler Ute   Distl Ottmar   Leeb Tosso  

Neurogenetics, Vol. 5, Iss. 1, 2004-02 ,pp. : 19-25

Springer Publishing Company

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Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A

By Fallet-Bianco Catherine  

Brain, Vol. 131, Iss. 9, 2008-09 ,pp. : 2304-2320

Oxford University Press

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Cellular Prion Protein (PrP^C) of the Neuron Cell Transformed to a PK-Resistant Protein Under Oxidative Stress, Comprising Main Mitochondrial Damage in Prion Diseases

By Yuan Fangzhong   Yang Lifeng   Zhang Zhuming   Wu Wenyu   Zhou Xiangmei   Yin Xiaomin   Zhao Deming  

Journal of Molecular Neuroscience, Vol. 51, Iss. 1, 2013-09 ,pp. : 219-224

Humana Press, Inc

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