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As the motor array in our nanomachine spans 523 ± 175 nm, the structural condition for performance optimisation is one HMM available every ((523 ± 175)/15 = ) 34.9 ± 11.7 nm of actin filament.
An alternative frequency-dependent approach was explored for a single array in our previous works [15, 16], using either a time domain implementation or a frequency domain implementation.
In life, there are many things we can't control, things that will inevitably go array in our days, but this didn't have to be one of them.
We have chosen the mappings from probe to transcript protein mapping (IPI identifier) provided in [39] for the U133A human array in our analysis.
Our group initially developed and validated a BAC/PAC array in our clinical cytogenetics laboratory for Chromosomal Microarray Analysis (CMA V4) [24].
We sought to assess whether the HHL APEX array provides additional value as a diagnostic tool and to determine the frequencies of mutations included on the array in our participants with congenital NSNHL.
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Based on our experimental results, the growth of carbon nanotube arrays in our experimental condition could not be diffusion-limited.
In our experiment, when ZnFe2 alloy nanowires were post-oxidation annealed, defects and the disorder of cation redistribution on A- and B- sites may occur, which can induce the magnetization for ZnFe2O4 nanowire arrays in our case.
Compared with the SiC nanowire arrays in our former work [[24]], we supposed that the position of the AAO template and the reaction time have palyed important roles in determining the morphology of the products.
It is seen that the SiNP arrays with length of ~600 nm are vertically aligned on Si surface and no SiNP bundles or clumps can be observed on Si surface, implying an effective method to fabricate large-area PASiNP arrays in our study.
This is expected because we analyzed many more mouse arrays in our study (2145 vs. 388 mouse arrays).
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