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As it may be observed, patterns may exist for larger values of ν1 as ν2 also gets larger, i.e., as the glycolytic flux increases.
As expected, identical Sau3A I patterns were observed in wildtype and DAM-expressing strains (compare Sau3A I lanes in Figs. 2c versus 2d, and 2i versus 2j).
We emphasize that patterns (i)–(iv) were observed even for multiexon duplogs.
That means the data pattern you are observing now is indeed special.
DOI: http://dx.doi.org/10.7554/eLife.04581.009 The periodic structure was only observed in axons, but not in dendrites, during early developmental stages, whereas isolated patches of periodic βII spectrin patterns were observed in dendrites during later developmental stages.
This finding was classified as type I according to Sano's classification [ 4] and Kudo type IIIL or elongated type I pit pattern was observed with magnifying chromoendoscopy and crystal violet staining (0.05%).
The following were observed: i) Typical track patterns were determined according to features of LDRT profiles, four patterns for left-hand bends and five patterns for right-hand bends, which can be used to identify crash prone position and reveal the mechanism of crash.
In fact, in Fig. 2c highly crystallized diffraction pattern was observed from SAED pattern.
No difference patterns were observed in endometrial histological/cytological patterns.
In contrast, negligible recurrence was observed for neuronal patterns obtained when animals explored a familiar environment.
However, few differences were observed in EMG patterns between conditions.
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