The procedure described here is designed to eliminate these drawbacks.
The procedure described here is significantly improved in time consumption, recovery, and purity.
The experimental procedure described here facilitates the high level production of recombinant glucagon with an extended biological activity.
As a result of the procedure described here, the collaborator has been able to reproduce the results with great accuracy.
The MD simulation procedure described here is similar to our previous work as canbe seen in [15].
The experimental procedure described here can be generalized to other systems and allows to locate the performance limitations.
The decellularization procedure described here lead to the preservation of the native extracellular matrix architecture and the removal of cells.
The main hypothesis motivating the procedure described here is that the partial frequencies of a given instrument or vocal vary approximately in the same way with time.
Naturally the procedure described here also removes a large amount of acceptable data in the context of many assays but this is unavoidable.
By using the procedure described here, the coefficients of the basis functions can be obtained directly by solving an uncoupled ordinary differential equation.
The procedure described here utilizes native-space morphometry as well as a method for dividing the insula into connectivity-based sub-regions estimated from cytoarchitectonics.
