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Accordingly, the transmission probability of synchronous and asynchronous STAs in each C i can be calculated as follows: (21).
By the induction assumption, we see that for, i = 1, …, v, the position of the integer in each C h i such that it is the optimal successor of two integers in C h + 1, i is the same, respectively.
After performing integration over all the possible values of a k, n in each C M j constellation, we find that E [ | Y k, n | ∕ ε k, n = 1 ] = π 2 1 4 ∑ j = 1 4 1 M j ∑ p = 1 M j ∑ l σ h ( l ) 2 E s | c p | 2 + σ w 2, (56).
Total EB positivity (pixels) in each c hippocampus and d frontal cortex.
Then, m/ z values of all fragments in each C and corresponding C MS/MS spectrum are sorted in descending order.
The operations to execute the fully enumerating algorithm depend on N e, N C, and the length of the elements in each c i, which are inherently random so we shall refer to the mean length c avg.
Similar(54)
Cross peaks are at the intersection of the C and H shifts of the partners in each C-H pair.
Therefore, we compared the Sse and Acc composition in each C-terminal position of T4S effectors with those of the non-T4S proteins.
In the holoenzyme complex, RI subunits position an inhibitor peptide in place of substrate in each C-subunit loaded with an ATP molecule and two Mg2+ ions.
This phosphoacceptor arginine, already observed by Anderson et al. (2010) as invariably conserved in each C-terminal region of their SRR supradomains, does occur in each sr2 domain.
Despite the sequences in each C+ branch containing the seven residue indel characteristic of the C+ group and sequences in each C- IV) branC- IVcking the indel, the branches have a higher average sequence identity (56%, 46%, 60%, respectivelackingn in general would be expecthe for a C+ and a C-(indelroup (~40%).
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