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Alternatively, complex diseases such as end stage heart failure are characterized by a number of abnormalities at the cellular level, many of which can be targeted using gene delivery to alter myocardial protein levels.
Alternatively complex glycans may themselves carry a negative charge, by virtue of attached sialic acid, whose effect could again be mitigated by the presence of positive charges near the glycosylation site.
Alternatively, complex multiallelic/mosaic regions can result from gene conversion which can change the CN profile from that of the parents [ 83], an observation consistent with the several examples of de novo CNVs described in this study.
This might reflect anomalous running of this particular glycoform of P2X2; it might be possible that full EndoH cleavage was not achieved in this sample or, alternatively, complex glycosylation might be added to Asn or Asn, but only when Asn contains complex glycosylation.
Alternatively, complex I turnover (NADH ubiquinone oxidoreduction) is a well-defined reaction that occurs at up to ∼200 s–1 (∼400 electrons transferred down the chain per second) in isolated complex I. Consequently, the maximum possible half-transfer time is 1.7 ms (if, which is highly unlikely, intramolecular electron transfer is fully rate limiting).
Alternatively, complex I NADH Q1 oxidoreductase activity was assessed: 25 μg SMP were diluted in 1 ml PBS pH 7.5 supplemented with 10 μM NADH to convert the enzyme to the A-form. 1 mM KCN, 30 μM Q1 and 165 μM NADH were then added to the suspension and the NADH oxidation rate was measured in the linear part of the curve.
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But a Lie group is also a smooth manifold, as described in the supplement A Modern Formulation of Riemann's Theory: the set G can be represented patchwise by systems of real-valued (or alternatively complex-valued) coordinates, mutually linked by well-defined, differentiable coordinate transformations wherever their respective patches overlap.
Alternatively, complexes might be brought together by an RNA component, and again there are several precedents and possibilities, including short interfering RNA or antisense non-coding transcripts [68] [72].
Alternatively, complexes of the [99mTc(CO 3]1+-core are partiCO 3]1+-coreresting since they are derived from the particularly9mTc(CO)3(OH2)3]+, whinterestingrganometallic intermediate with three labile water moleculesincebling coordinathey of bidentare or triderived ligands [ 36].
Alternatively, the complex domain could be lost entirely, resulting in a novel low-complexity gene lineage.
Alternatively, the complex signature from external fields is considered as contributing to the data error budget when recovering main field changes from the annual means series starting in 1840 (Jackson et al. 2000).
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