This pattern is also seen when facial expressions are simply imagined (Kim et al., 2007).
Labyrinthine patterns are also seen when the Heaviside firing rate function is replaced by a steep sigmoid, as will be discussed later.
These patterns were also seen when stratifying by sex (Table 3).
Unusual patterns are also seen when comparing the single and double BER knockdowns, and the patterns seen for PCNA and ATR are hard to interpret, again because of the fluctuation in the 0-mismatch substrate.
Size dependency was also seen when measuring mechanical properties of these ASMs.
The same pattern was also seen in a reciprocal comparison, when levels of dN and dS for human and mouse orthologs were compared to levels of dN and dS for mouse paralogs (data not shown).
This pattern was also seen in KNE.
A tendency towards this pattern was also seen in HepG2.
The same pattern was also seen in the FTRCT patients.
A similar pattern of lesion formation is also seen when myelin and oligodendrocytes are destroyed through antigen-specific cytotoxic T-cells [ 164] or non-selectively by toxic products of activated macrophages (bystander demyelination).
