Results 241 to 250 of about 69,281 (285)

Mutational Analysis Supports Three-Hairpin Model of Attenuator for Transcription Regulation of ilvBNC Operon in Corynebacterium glutamicum. [PDF]

Microorganisms
Ryabchenko LE, Titov II, Leonova TE, Kalinina TI, Gerasimova TV, Sheremetieva ME, Kolchanov NA, Khlebodarova TM, Yanenko AS.   +8 more
europepmc   +1 more source

Bacteria as living biosensors for DNA. [PDF]

Nat Rev Bioeng
O'Connor K, Steppe P, Worthley D, Hasty J, Cooper R.   +4 more
europepmc   +1 more source

RAPID-DASH: fast and efficient assembly of guide RNA arrays for multiplexed CRISPR-Cas9 applications. [PDF]

Synth Biol (Oxf)
Salaudeen AL, Mateyko N, de Boer CG.
europepmc   +1 more source

Toehold-VISTA: a machine learning approach to decipher programmable RNA sensor-target interactions. [PDF]

Nucleic Acids Res
Robson JM, Green AA.
europepmc   +1 more source

Engineering the Caenorhabditis elegans genome with a nested, self-excising selection cassette. [PDF]

Genetics
Gibney TV, Pani AM.
europepmc   +1 more source

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Release Factor Translation of RNA Phage Terminator Codons

Nature, 1970
Release factors R1 or R2 stimulate equally well the release of f2 coat protein, suggesting that UAA is the first coat terminator codon. The suppression of a nonsense codon can be regulated in vitro by the concentration of R factor of appropriate codon specificity.
A L, Beaudet, C T, Caskey
openaire   +4 more sources

Selective differences among translation termination codons

Gene, 1988
The frequency of use of the three alternative translation termination codons has been examined in 165 Escherichia coli, 52 Bacillus subtilis and 106 Saccharomyces cerevisiae genes. Genes were first categorised according to their degree of bias in sense codon usage. In each species there is a very strong bias in favour of UAA (over UAG and UGA) in genes
P M, Sharp, M, Bulmer
openaire   +2 more sources