However, the differences in weight were not large and may represent differences in timing of responses as much as fundamental differences in response.
In this respect genes that only agreed with one platform in terms of differential expression or were only seen in RNA-Seq may represent differences in transcript isoform abundances.
This may represent differences in parasite detection thresholds, as parasite positive individuals at enrollment were identified by PCR amplification, and thus harboured lower density parasitaemia on average versus positives identified by blood film examination during ADI.
Increases in ARC Kiss1 mRNA was not found in our study in intact mice between P10 and P30 and may represent differences in species, time points studied, or methodology in qRT-PCR expression normalization; e.g. in our protocol we controlled for developmental changes in ARC size.
The differences in validity between studies may represent differences in operational characteristics of the study samples.
Such variability may represent differences in study populations or may relate to diagnostic difficulty.
This may represent differences in equilibrium levels for BA homeostasis between individuals.
This may represent differences in electrochemical vs spectroscopic detection associated with analyte absorption.
These differences may represent differences in Al stress perception and adaptation in T32 and S70 root tips.
These associations between maternal factors and hypothyroidism may represent differences in the health of the maternal populations.
