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期刊名:Prion

缩写:PRION

ISSN:1933-6896

e-ISSN:1933-690X

IF/分区:1.7/Q4

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共收录本刊相关文章索引737
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Daniel W Summers,Peter M Douglas,Douglas M Cyr Daniel W Summers
Molecular chaperones regulate essential steps in the propagation of yeast prions. Yeast prions possess domains enriched in glutamines and asparagines that act as templates to drive the assembly of native proteins into beta-sheet-rich, amylo...
Laura R Moody,Allen J Herbst,Han Sang Yoo et al. Laura R Moody et al.
Identification of genes expressed in response to prion infection may elucidate biomarkers for disease, identify factors involved in agent replication, mechanisms of neuropathology and therapeutic targets. Although several groups have sought...
Karine Gousset,Chiara Zurzolo Karine Gousset
The discovery of tunnelling nanotubes (TNTs) and their proposed role in long intercellular transport of organelles, bacteria and viruses have led us to examine their potential role during prion spreading. We have recently shown that these m...
Yukiko M Yamashita Yukiko M Yamashita
Asymmetric stem cell division is a mechanism widely employed by the cell to maintain tissue homeostasis, resulting in the production of one stem cell and one differentiating cell. However, asymmetric cell division is not limited to stem cel...
Wendy Noble,Claire J Garwood,Diane P Hanger Wendy Noble
Many neurodegenerative disorders share common features including the accumulation of aggregated misfolded proteins, neuroinflammation and the induction of apoptosis. While the contributions of each of these individual elements to neuronal d...
Bess Frost,Marc I Diamond Bess Frost
The aggregation of a soluble protein into insoluble, beta-sheet rich amyloid fibrils is a defining characteristic of many neurodegenerative diseases, including prion disorders. The prion protein has so far been considered unique because of ...
Peter M Douglas,Daniel W Summers,Douglas M Cyr Peter M Douglas
The self-association of misfolded or damaged proteins into ordered amyloid-like aggregates characterizes numerous neurodegenerative disorders. Insoluble amyloid plaques are diagnostic of many disease states. Yet soluble, oligomeric intermed...
Matthew F Calabrese,Andrew D Miranker Matthew F Calabrese
Beta-2 microglobulin (beta2m) is the protein responsible for amyloid deposition in Dialysis-Related Amyloidosis (DRA). Aggregation can be induced by various solution conditions including exposure to divalent metal, incubation at acidic pH, ...
James A Huntington,Timothy J Sendall,Masayuki Yamasaki James A Huntington
We recently solved the crystallographic structure of a dimeric form of the serpin antithrombin which has fundamentally changed the way we think about serpin polymerization. Like for other diseases that have protein deposition as a hallmark,...
Alexander Rubinstein,Yuri L Lyubchenko,Simon Sherman Alexander Rubinstein
The structural organization of the amyloidogenic beta-protein containing 40 amino acid residues (Abeta40) was studied by the high temperature molecular dynamics simulations in the acidic (pH approximately 3) and basic (pH approximately 8) p...