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05). However, ��1A?/?/PC-��1ACTWT mice exhibited the same three patterns of CF contacts seen with ��1A?/? mice, mono CF on PC dendrites, multiple CF contacts on proximal dendrites, and multiple CF contacts on PC soma ( Figure?5). These results demonstrate that ��1ACT, as a transcription factor, plays an important role in establishing normal dendritic tree morphology in PCs in?vivo [http://www.selleckchem.com/products/Thiazovivin.html Selleckchem Thiazovivin] but that synapse elimination or selection of dominant innervation requires either P/Q channel function or ��1ACT under its endogenous expression pattern. Finally, we examined mRNA levels of TAF, BTG1, PMCA2, and GRN in the three mouse groups. Figure?S5 demonstrates that the expression of these genes was decreased in cerebellar tissue of ��1A?/? mice when compared to normal mice but was increased 1.5- to 3-fold in ��1A?/?/PC-��1ACTWT transgenic mice when compared to ��1A?/? mice (p?[http://www.selleckchem.com/TGF-beta.html TGF-beta family] EPSCs from ��1A?/?/PC-��1ACTWT mice were greater than those from ��1A?/? mice (p?[http://en.wikipedia.org/wiki/Laccase Laccase] et?al., 1995). We therefore examined the presynaptic release properties of PF-PC synapses in ��1A?/? and ��1A?/?/PC-��1ACTWT mice by measuring the paired-pulse ratios (PPRs) of PF-EPSCs. Large PPRs are indicative of low initial release probabilities and are a sign of impaired presynaptic function ( Zucker and Regehr, 2002). In accordance with observations from mouse models harboring loss-of-function mutations in the CACNA1A gene, ��1A?/? mice exhibited PPRs significantly greater than WT at several stimulus intervals (WT to ��1A?/? mice: p?