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The unique structural features such as tunable structure and molecular size, large number of accessible terminal functional groups, and ability to encapsulate cargos add to their potential as drug carriers [ 57].
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However, many require publicly accessible terminals, which are not very common and a limiting factor in rail freight transport.
The system will be accessible via terminal or a remote desktop solution using full hardware acceleration.
The first approach towards alkene 6 started with acetonide protection of d-ribose (9) as outlined in Scheme 2. Initially, we intended to install the alkene moiety required for the cross-metathesis reaction by Tebbe olefination of the corresponding methyl ketone, which should be accessible from terminal alkene 14 after Wacker oxidation.
Consistent with this, the Murid Herpesvirus-4 (MuHV-4) gB switches during entry from having readily accessible N-terminal epitopes and poorly accessible epitopes involving C-terminal domains to the converse [13].
But the British Library archive will only be accessible from terminals in its building, raising questions over the Tory commitment to transparency.
However, the presence of Sec in TrxR at an easily accessible C-terminal position renders the enzyme highly susceptible to irreversible inhibition by derivatization of the Sec residue.
NR2E3/CRX interactions analyzed by BRET2 also showed the importance of a freely accessible N-terminal DBD of CRX to interact with NR2E3.
These are carbohydrate-active molecules that, though predominantly found in soluble form within the cytosol, are capable of localizing to bacterial and fungal cell walls where they exhibit accessible carboxyl-terminal or internal lysine residues for plasminogen binding [49].
The kringle domains of plasminogen structure are ∼80 amino acids in length and mediate the attachment of plasminogen to cell surfaces by binding proteins with accessible carboxyl-terminal or internal lysine residues.
The loosening of DNA-histone interactions and the subsequent unmasking of transcription factor binding sites is controlled by specific covalent modifications of accessible N-terminal histone tails.
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