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To assess whether social isolation was a necessary precondition for the SCPP phenotype to be expressed, juvenile B6 mice were subjected to the social conditioning procedure used for Experiment 2 with the order of conditioning sessions (social or isolate housing) reversed.
We then expressed juvenile to adult survival (for individuals maturing at ages 3 5) as: 5 Note that all individuals of each tactic have a common survival through the third year, and survival in subsequent years was determined by proportioning remaining to breed and ocean survival.
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In agreement with previous studies, our observations show that in both E. grandis and E. brachyphylla, a relatively high level of miR156 is expressed in juvenile tissues, although no marked changes in leaf shape between the juvenile and mature phases were observed in these Eucalyptus trees, as reported for example for E. globulus [ 15].
Many of the genes expressed in juvenile and adult baboon ovaries are also likely to be expressed in juvenile and adult ovaries of other primates, including humans.
Out of the 96 randomly-chosen, putative juvenile clones, 53 were only expressed in juveniles, 13 were expressed at a higher level in juveniles than in adults, 5 were expressed at similar levels in adult and juveniles and 25 did not generate any signal with either probe (Fig 2., top panels).
Genes more expressed in juvenile wood include methionine synthase, HB1, cytochrome c oxidase, alpha tubulin 1, metallothionein-like, AGP6, etc.
ICA positivity was expressed in Juvenile Diabetes Foundation units (JDF-U) by a standard curve based on the international JDF-U reference sera sample.
As males are a common reference, this indicates that a significant number of genes were also differentially expressed in juvenile females relative to mature females.
To complement this set of ESTs, we decided to seek for genes that are differentially expressed in juvenile and mature secondary xylem tissues.
Using this approach, and by comparing male replicates to each other as a control, we identified genes differentially expressed between juvenile and pregnant females (Fig. 3A).
We then examined migration profiles of 17 major components of the molecular motors from five kinesin families excluding kinesin-4 which is mostly expressed in juvenile brain, cytoplasmic dynein and dynactin.
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