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Using the above forms of scale factors, the Ricci scalar R Open image in new window is reconstructed as follows: For emergent scenario: R = 6 − B 2 e 2 Bt n ( e Bt + η ) 2 + 2 B 2 e 2 Bt n 2 ( e Bt + η ) 2 + B 2 e Bt n e Bt + η + k ( e Bt + η ) − 2 n A 2 Open image in new window (22).
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A generalization to the Viterbi algorithm can now be directly implemented, using the above form, to establish an efficient dynamic programming table construction.
Also, optical nonlinearity saturates at a finite value of optical intensity in most materials and the soliton propagation in semiconductor-doped fibers can be modeled using the above form.
By using the above form (23) we again obtain two boundaries on the entry costs, i.e. (24) F ̲ OL : = C 2 − B 2 2 4 A 2, F ¯ OL : = C 2. The interpretation is analogous to the Markov perfect equilibrium, only the levels are different.
By using the above alternative forms, we derive some new identities for the Bernstein basis functions.
Using the above stabilization form, a semi-discrete CIP Galerkin approximation of optimal control problem (2.1 - 2.2 2.1 - 2.2ed by mis u h ∈ U a defined h, u h ) (2.11).
Next, we evaluated whether an inhibitory ANXA2-targeted monoclonal antibody can suppress Panc02 hepatic metastases using the above described liver metastases forming mouse model.
In every genome containing two divergent S4 genes, the C+ form is located in the α-operon and the C- IV) or C- IV form outside. Using the above C- Veria, we C- Vlude that the C+ form is the outsidel S4 sequence and the C- form the paralog in these genomes.
In order to calculate the unknown coefficients (c_{k}) in linear system (3.5), we rewrite this system by using the above notations in matrix-vector form as mathbf{A}mathbf{c}=mathbf{B} (3.6) where Now we have a linear system of n equations in the n unknown coefficients given by (3.6).
We substituted the know zenith angles and derived the percent of previtamin D3 and vitamin D3 formed using the above equation.
For SSCP analysis, 1 μl of each PCR product formed using the above mentioned PCR program and primers, was mixed with 9 μl SSCP loading buffer (98% v/v, formamide, 10 mM EDTA+0.05% Bromo-Phenol Blue+0.5% Xylene Cyanol) and incubated at 90°C for 5', followed by rapid cooling on ice. 10 μl of this mixture was loaded on a 6% acrylamide gel containing 1XTrisborate EDTA buffer.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com