Prion, Volume 10, Issue 6 (2016)

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Prion, Volume 10, Issue 6 (2016)

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Article Commentary
Transmissibility of Gerstmann–Sträussler–Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity
Romolo Nonno, Michele Angelo Di Bari, Umberto Agrimi & Laura Pirisinu
Pages: 421-433
Published online: 28 Nov 2016
AbstractforTransmissibility of Gerstmann–Sträussler–Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity | Full Text | References | PDF (393.6 KB)
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Article Commentary
Misfolding leads the way to unraveling signaling pathways in the pathophysiology of prion diseases
Berta Puig, Hermann C. Altmeppen & Markus Glatzel
Pages: 434-443
Published online: 21 Nov 2016
AbstractforMisfolding leads the way to unraveling signaling pathways in the pathophysiology of prion diseases | Full Text | References | PDF (594.4 KB)
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Research Papers

Article
The small heat shock protein Hsp31 cooperates with Hsp104 to modulate Sup35 prion aggregation
Kiran Aslam, Chai-jui Tsai & Tony R. Hazbun
Pages: 444-465
Published online: 03 Oct 2016
AbstractforThe small heat shock protein Hsp31 cooperates with Hsp104 to modulate Sup35 prion aggregation | Full Text | References | PDF (1,014.8 KB)
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Article
Role of polysaccharide and lipid in lipopolysaccharide induced prion protein conversion
Carol L. Ladner-Keay, Marcia LeVatte & David S. Wishart
Pages: 466-483
Published online: 01 Dec 2016
AbstractforRole of polysaccharide and lipid in lipopolysaccharide induced prion protein conversion | Full Text | References | PDF (811.2 KB) | Supplemental
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Short Communication

Rapid Communication
Quality evaluation for the surveillance system of human prion diseases in China based on the data from 2010 to 2016
Qi Shi, Wei Zhou, Cao Chen, Chen Gao, Kang Xiao, Jing Wang, Bao-Yun Zhang, Yuan Wang, Feng Zhang & Xiao-Ping Dong
Pages: 484-491
Published online: 03 Oct 2016
AbstractforQuality evaluation for the surveillance system of human prion diseases in China based on the data from 2010 to 2016 | Full Text | References | PDF (498.8 KB)
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Case Reports

Case Report
An autopsy-verified case of FTLD-TDP type A with upper motor neuron-predominant motor neuron disease mimicking MM2-thalamic-type sporadic Creutzfeldt-Jakob disease
Yuichi Hayashi, Yasushi Iwasaki, Akira Takekoshi, Nobuaki Yoshikura, Takahiko Asano, Maya Mimuro, Akio Kimura, Katsuya Satoh, Tetsuyuki Kitamoto, Mari Yoshida & Takashi Inuzuka
Pages: 492-501
Published online: 08 Dec 2016
AbstractforAn autopsy-verified case of FTLD-TDP type A with upper motor neuron-predominant motor neuron disease mimicking MM2-thalamic-type sporadic Creutzfeldt-Jakob disease | Full Text | References | PDF (727.1 KB)
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Case Report
Familial Creutzfeldt-Jakob Disease: Case report and role of genetic counseling in post mortem testing
Kristin Clift, Kimberly Guthrie, Eric W. Klee, Nicole Boczek, Margot Cousin, Patrick Blackburn & Paldeep Atwal
Pages: 502-506
Published online: 08 Dec 2016
AbstractforFamilial Creutzfeldt-Jakob Disease: Case report and role of genetic counseling in post mortem testing | Full Text | References | PDF (48 KB)
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