Exact(60)
We have previously documented that diabetes patients of lower SES experience higher morbidity and mortality [39, 40].
Among men with clinically low-risk prostate cancer, we have previously documented heterogeneity in terms of clinical characteristics and genomic risk scores.
However, patients cannot be ascribed to such discrete binary categories (rare v. common, multi-infected v. otherwise healthy), and we have previously documented various Mendelian traits predisposing to a single type of infection.
In addition, we have previously documented lower mating propensity in the stonewort ecotypes [21].
However, we have previously documented interactions between DLC1 and the tensin2 PTB domain [38].
We attribute these phenotypic differences among the strains to the high degree of genomic plasticity that we have previously documented.
Thus, the expansion of the stem/progenitor cells in the SVZ that we have previously documented may not be sufficient to replenish damaged white matter oligodendrocytes progenitors.
Furthermore, we have previously documented that spontaneous monocyte apoptosis is not dependent upon caspase-1 but upon caspase-3 activity [41].
We have previously documented an association between FGFR1 and FLRT1 [4] and we were interested to learn the cellular location(s) of this interaction.
These criteria are the same as we have previously documented and are more stringent than those recommended for the commercial T-spot assay[21].
This suggests that heat-evoked foot withdrawal in naked mole-rats is largely mediated via AMPA receptors and the presence of AMPA-mediated excitatory post-synaptic potentials in response to a noxious stimulus in the superficial dorsal horn of naked mole-rat spinal cords is something we have previously documented [5].
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