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The period of these oscillation differed from mouse to mouse, but the oscillatory periods were quite similar among islets from the same mouse, which indicates imprinting.
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Total adrenal weight did not differ from control mice (control mice 3.62 ±.27 mg, UCN3OE 3.69 ±.33 mg, n = 6 8).
The CAP recorded from P120 transgenic mice differed from P40 mice in that the amplitudes of the peaks were smaller.
For example, Boehm and colleagues (2004) found that mice in which the GABAA-R α2 subunit had been deleted (i.e., α2 knockout mice) differed from control mice both in behavioral tests conducted without alcohol exposure (e.g., showed decreased spontaneous locomotion when tested for locomotor response to novelty) and in some behavioral responses to alcohol.
When C57BL/6J-Chr 11A/J/ NaJ mice were fed a HFHC diet for 8 wk, both hepatic Xbp1s and Socs3 gene expression was similar to A/J mice, yet differed from C57BL/6J mice.
In several of these measures, XX mice also differed from XY mice, and gonadal males and females differed significantly on almost every metabolic measure.
When anxiety-related behavior was analyzed, neither young nor adult Syn KO mice significantly differed from control mice in the number of central entries (Fig. 1B).
Moreover, while traveling similar distances, NAB mice also clearly differed from LAB mice in anxiety-related parameters, further supporting the critical role of anxiety (rather than locomotor effects) in the behavioral divergence among HAB, NAB and LAB animals as observed in the OA exposure test.
This sequence differs from mouse by one amino acid.
In every case, the response of TRPV1 knockout mice to nicotine did not differ from wildtype mice, indicating that these mice were capable of detecting and responded to trigeminal irritants normally.
MRL/ lpr mice differ from MRL mice with respect to a mutation involving the Fas gene [ 26]; however, negative selection in the thymus does not seem to be impaired in either strain [ 27].
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