Expanding the genetic code of Escherichia coli with phosphotyrosine
, 2016 Chenguang Fan, Kevan Ip, Dieter Söll
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Genetic Algorithm model and data files to assess JONSWAP spectra coefficients: MATLAB code
, 2020 Juan Gabriel Rueda-Bayona +1 more
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BMI‐1 modulation and trafficking during M phase in diffuse intrinsic pontine glioma
FEBS Open Bio, EarlyView.The schematic illustrates BMI‐1 phosphorylation during M phase, which triggers its translocation from the nucleus to the cytoplasm. In cycling cells, BMI‐1 functions within the PRC1 complex to mediate H2A K119 monoubiquitination. Following PTC596‐induced M phase arrest, phosphorylated BMI‐1 dissociates from PRC1 and is exported to the cytoplasm via its
Banlanjo Umaru +6 more
wiley +1 more source
Strategies to Expand the Genetic Code of Mammalian Cells. [PDF]
Chem RevOsgood AO +3 more
europepmc +1 more source
Meta‐analysis fails to show any correlation between protein abundance and ubiquitination changes
FEBS Open Bio, EarlyView.We analyzed over 50 published proteomics datasets to explore the relationship between protein levels and ubiquitination changes across multiple experimental conditions and biological systems. Although ubiquitination is often associated with protein degradation, our analysis shows that changes in ubiquitination do not globally correlate with changes in ...
Nerea Osinalde +3 more
wiley +1 more source
A super versatile flexizyme system with phenol esters for genetic code reprogramming. [PDF]
Nat CommunChoi YK, Katoh T, Beattie A, Suga H.
europepmc +1 more source
Are the Strange Information Structures of the Genetic Code an Accident or an Artifact? [PDF]
Alexander Panov, Felix P. Filatov
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Switchable genome editing via genetic code expansion [PDF]
, 2018 Toru Suzuki +5 more
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SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source
Genetic code expansion and enzymatic modifications as accessible methods for studying site-specific post-translational modifications of alpha-synuclein and tau. [PDF]
Protein SciSaleh IG +17 more
europepmc +1 more source