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The P3200's exploitation of the T-grain technology's capacity for higher speeds may overcome such qualms.
Methods recently developed for scaffold-free 3D bioprinting may overcome such obstacles and should allow for rapid manufacture and deployment of "bioprinted organs".
Three-dimensional images using SPECT/CT may overcome such a problem by fusing functional and morphological images [23,24].
More comprehensive approaches such as the use of population-based surveys may overcome such hurdles in shedding more light on the burden of injury recidivism.
Discovery and exploitation of structurally different new types of antimicrotubule agents may overcome such problem.
The measurement of cancer associated mutations in the entire mtgenome may overcome such limitations.
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Nanoparticular drug delivery systems, on the other hand, may help overcome such drawbacks and improve the efficacy of anti-angiogenic therapies by altering the biodistribution and pharmacokinetics, improving tumor targeting ability, and reducing side effects.
Thus, newer serological tests based on protein antigen and or combination of protein antigen by combination of suitable IgM, IgG, or IgA may eventually overcome such difficulties.
On the other hand de novo assembly approaches may theoretically overcome such problems, but pose a number of challenges due for example to repetitive sequences, low complexity sequences and closely related paralogs [ 12].
Incorporating techniques used in scaffold-hopping, such as using reduced graphs, may help to overcome such limitations[ 23].
In both cases the use of paired end/mated pair sequencing approaches may help to overcome such shortcomings in the future.
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CEO of Professional Science Editing for Scientists @ prosciediting.com