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Chaperone-dependent amyloid assembly protects cells from prion toxicity.
Proceedings of the National Academy of Sciences of the United States of America May, 2008 | Pubmed ID: 18480252
A systematic survey identifies prions and illuminates sequence features of prionogenic proteins.
Cell Apr, 2009 | Pubmed ID: 19345193
Prions, protein homeostasis, and phenotypic diversity.
Trends in cell biology Mar, 2010 | Pubmed ID: 20071174
Biochemical, cell biological, and genetic assays to analyze amyloid and prion aggregation in yeast.
Methods in enzymology , 2010 | Pubmed ID: 20946833
Epigenetics in the extreme: prions and the inheritance of environmentally acquired traits.
Science (New York, N.Y.) Oct, 2010 | Pubmed ID: 21030648
A method for probing the mutational landscape of amyloid structure.
Bioinformatics (Oxford, England) Jul, 2011 | Pubmed ID: 21685090
Opposing effects of glutamine and asparagine govern prion formation by intrinsically disordered proteins.
Molecular cell Jul, 2011 | Pubmed ID: 21726811
Prions are a common mechanism for phenotypic inheritance in wild yeasts.
Nature Feb, 2012 | Pubmed ID: 22337056
A glass menagerie of low complexity sequences.
Current opinion in structural biology 06, 2016 | Pubmed ID: 27258703
A self-perpetuating repressive state of a viral replication protein blocks superinfection by the same virus.
PLoS pathogens 03, 2017 | Pubmed ID: 28267773
Quantifying Nucleation In Vivo Reveals the Physical Basis of Prion-like Phase Behavior.
Molecular cell 07, 2018 | Pubmed ID: 29979963
Structures of autoinhibited and polymerized forms of CARD9 reveal mechanisms of CARD9 and CARD11 activation.
Nature communications Jul, 2019 | Pubmed ID: 31296852
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