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Compared to the size of the cavity, MD and 4-NBT are small molecules and do not fully interact with most of the residues lining the wall of the dimer interface.
Drugs of abuse are small molecules and do not induce antibodies following injection or inhalation.
γδ TCRs appear to recognize antigen directly, similar to immunoglobulins (Igs), but they do not require presentation by an MHC protein or other molecules and do not depend on antigen processing.
Because most of the plasmids analyzed are relatively small molecules and do not harbor tra and/or mob genes, it is plausible that they might have been transmitted through transformation and/or transduction, the latter by uptake in a bacteriophage.
These "resident" macrophages have avid phagocytic and bacteriocidal activity but do not express innate response receptors or co-stimulatory molecules and do not produce inflammatory cytokines in response to microbial stimulation [ 29, 35].
The terms A and R refer only to free molecules and do not include those contained in complex C. The corresponding mRNA concentrations for activator and repressor are A m and R m. Continuous concentrations are assumed throughout.
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(26) We, therefore, only studied upright standing 2P molecules and did not consider any geometries with 2P lying flat on the SAM.
These characteristics were obtained for separated XG molecules and did not include the increase of height as the result of assembling.
Analytical gel filtration, dynamic light scattering and non-reducing gel electrophoresis confirmed that rhTRAILWT and variants were stable trimeric molecules and did not form higher-order molecular weight aggregates.
In other words, antigen capture was an integral part of the biosynthetic itinerary of class II MHC molecules and did not, for the most part, utilise a class II MHC recycling pathway we had recently demonstrated [23, 24].
Conversely, this finding may be reasonable if REG I α plays a role as only one of several antiapoptotic molecules, and does not activate multidrug transporter proteins or chemotherapeutic drug-metabolising enzymes.
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