Results 41 to 50 of about 19,763 (281)

Deep mutational scanning of RNA polymerase

open access: yes, 2023
RNA polymerase deep mutational scanning data accompanying the manuscript titled: Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and ...
Choudhury, Alaksh, Tenaillon, Olivier
openaire   +1 more source

Activation-induced deoxycytidine deaminase (AID) co-transcriptional scanning at single-molecule resolution [PDF]

open access: yes, 2015
Activation-induced deoxycytidine deaminase (AID) generates antibody diversity in B cells by initiating somatic hypermutation (SHM) and class-switch recombination (CSR) during transcription of immunoglobulin variable (IgV) and switch region (IgS) DNA ...
Bertram, JG   +7 more
core   +1 more source

Exploring amino acid functions in a deep mutational landscape

open access: yesMolecular Systems Biology, 2021
Amino acids fulfil a diverse range of roles in proteins, each utilising its chemical properties in different ways in different contexts to create required functions.
Alistair S Dunham, Pedro Beltrao
doaj   +1 more source

TITER: predicting translation initiation sites by deep learning. [PDF]

open access: yes, 2017
MotivationTranslation initiation is a key step in the regulation of gene expression. In addition to the annotated translation initiation sites (TISs), the translation process may also start at multiple alternative TISs (including both AUG and non-AUG ...
Hu, Hailin   +4 more
core   +1 more source

A high-affinity antibody against the CSP N-terminal domain lacks Plasmodium falciparum inhibitory activity [PDF]

open access: yes, 2020
Malaria is a global health concern and research efforts are ongoing to develop a superior vaccine to RTS,S/AS01. To guide immunogen design, we seek a comprehensive understanding of the protective humoral response against Plasmodium falciparum ...
Bosch, A.   +15 more
core   +2 more sources

Interpreting protein variant effects with computational predictors and deep mutational scanning

open access: yesDisease Models & Mechanisms, 2022
Computational predictors of genetic variant effect have advanced rapidly in recent years. These programs provide clinical and research laboratories with a rapid and scalable method to assess the likely impacts of novel variants.
Benjamin J. Livesey, Joseph A. Marsh
doaj   +1 more source

Deep mutational scanning: a new style of protein science [PDF]

open access: yesNature Methods, 2014
Mutagenesis provides insight into proteins, but only recently have assays that couple genotype to phenotype been used to assess the activities of as many as 1 million mutant versions of a protein in a single experiment. This approach-'deep mutational scanning'-yields large-scale data sets that can reveal intrinsic protein properties, protein behavior ...
Douglas M, Fowler, Stanley, Fields
openaire   +2 more sources

Comprehensive sequence-to-function mapping of cofactor-dependent RNA catalysis in the glmS ribozyme. [PDF]

open access: yes, 2020
Massively parallel, quantitative measurements of biomolecular activity across sequence space can greatly expand our understanding of RNA sequence-function relationships. We report the development of an RNA-array assay to perform such measurements and its
Andreasson, Johan OL   +3 more
core  

Rapid, ultra low coverage copy number profiling of cell-free DNA as a precision oncology screening strategy. [PDF]

open access: yes, 2017
Current cell-free DNA (cfDNA) next generation sequencing (NGS) precision oncology workflows are typically limited to targeted and/or disease-specific applications.
Alva, Ajjai S   +31 more
core   +1 more source

Deep mutational scanning of the plasminogen activator inhibitor-1 functional landscape

open access: yesScientific Reports, 2021
The serine protease inhibitor (SERPIN) plasminogen activator inhibitor-1 (PAI-1) is a key regulator of the fibrinolytic system, inhibiting the serine proteases tissue- and urokinase-type plasminogen activator (tPA and uPA, respectively).
Zachary M. Huttinger   +7 more
doaj   +1 more source

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