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Careful observation of morphological architecture and expression of immunohistochemical markers may support diagnosis.
However, the improvement of plasma levels of these surrogate markers may support our assumption of the good detoxification capacity of the procedure.
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Molecular markers may potentially support a differential diagnosis between FTC and FTA in postoperative specimens.
A commonplace issue that arises when carrying out case-control studies to detect genetic association is that more than one marker within the same gene may support association.
Our results may support the conclusion that MCM2 and MCM3 are better markers to evaluate tumoral behavior and more sensitive markers for the identification of proliferating cells than is Ki-67.
Gene expression profiling and the analysis of protein-protein interaction (PPI) networks may support the identification of disease bio-markers and potential drug targets.
This may support the theory.
These markers may therefore also be useful to support histopathologic diagnosis of metastatic deposits suspected of being melanoma.
Microsatellite markers may also, to some extent, support phylogenetic inferences.
Previous evidence has shown that interventions supported by surrogate markers may in fact have no benefit or even harmful effects on clinical outcome measures.
Furthermore, the hindlimb muscles showed earlier expression and activation of Smads compared to forelimb muscles providing further support that these markers may track disease progression.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com