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I recognize different kinds of limps from across the street and could tell you what part of your back is hurting just by seeing you walk across the room.
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For example, the RIG-I-like receptors (RLRs) RIG-I and MDA5 recognize different types of viral double-stranded RNA (dsRNA).
However, shortened poly IC is preferentially recognized by RIG-I rather than by MDA5 (Kato et al, 2008), suggesting that RIG-I and MDA5 recognize different lengths of RNA.
Studies in knockout animals demonstrated that the helicases RIG-I and MDA5 recognize different types of viruses, with MDA5 acting as the main receptor for cytoplasmic dsRNA in astrocytes (36) and β-cells (present data).
Furthermore, target recognition loops I and II recognize different parts of cognate GCGC sequences.
And now I'm able to recognize different emotions and I'm not governed by them.
The basis for these differences stems from the ability of RIG-I and MDA5 to recognize different RNA patterns.
RIG-I and MDA-5 recognize different length of viral double-stranded RNA (dsRNA) by their RNA helicase domain [ 6, 7].
Cross-reactivity is defined by the ability of a given T-cell population to recognize different peptide:major histocompatibility complex (MHC) class I complexes (pMHC-I).
It is thought that different receptor proteins "recognize" different parts of the molecule.
Different bacterial species make restriction enzymes that recognize different nucleotide sequences.
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CEO of Professional Science Editing for Scientists @ prosciediting.com