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期刊名:Progress in molecular biology and translational science

缩写:PROG MOL BIOL TRANSL

ISSN:1877-1173

e-ISSN:1878-0814

IF/分区:0.0/Q3

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共收录本刊相关文章索引1657
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
Neil A Mabbott Neil A Mabbott
Many natural prion diseases are acquired peripherally, such as following the oral consumption of contaminated food or pasture. After peripheral exposure many prion isolates initially accumulate to high levels within the host's secondary lym...
Alba Marín-Moreno,Natalia Fernández-Borges,Juan C Espinosa et al. Alba Marín-Moreno et al.
Transmissible spongiform encephalopathies (TSEs) are a group of progressive, invariably fatal diseases that affect the nervous system of many mammals including humans. The key molecular event in the pathogenesis of TSEs is the conversion of...
Abigail B Diack,James D Alibhai,Jean C Manson Abigail B Diack
The production of transgenic mice expressing different forms of the prion protein (PrP) or devoid of PrP has enabled researchers to study the role of PrP in the infectious process of a prion disease and its normal function in the healthy in...
Giuseppe Legname,Fabio Moda Giuseppe Legname
Transmissible spongiform encephalopathies or prion diseases are a group of fatal neurodegenerative diseases caused by unconventional infectious agents, known as prions (PrPSc). Prions derive from a conformational conversion of the normally ...
George A Carlson George A Carlson
Early genetic studies on scrapie, an infectious neurodegenerative disease of sheep that was adapted to mice, provided evidence in support of the hypothesis that the agent was a slow virus with a nucleic acid genome independent of the host. ...
Giulia Rossetti,Paolo Carloni Giulia Rossetti
Prion diseases, or transmissible spongiform encephalopathies, are a group of rare fatal neurodegenerative maladies that affect humans and animals. The main event in disease progression is the posttranslational conversion of the ubiquitously...
Théo Z Hirsch,Séverine Martin-Lannerée,Sophie Mouillet-Richard Théo Z Hirsch
Although initially disregarded compared to prion pathogenesis, the functions exerted by the cellular prion protein PrPC have gained much interest over the past two decades. Research aiming at unraveling PrPC functions started to intensify w...
Yuriko Osakabe,Keishi Osakabe Yuriko Osakabe
Targeted modification of specific genes via genome editing is now used routinely to modify plant genomes. In developing new mutations in plant genomes using the widely used CRISPR/Cas9 system, it is important for further use in plant molecu...
Honghao Bi,Bing Yang Honghao Bi
Engineered, site-specific nucleases induce genomic double-strand DNA breaks and break repair processes enable genome editing in a plethora of eukaryotic genomes. TALENs (transcription activator-like effector nucleases) and CRISPR/Cas (clust...