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. Author manuscript; available in PMC: 2011 Apr 1.
Published in final edited form as: J Neurochem. 2010 Feb 2;113(1):166–174. doi: 10.1111/j.1471-4159.2010.06594.x

Table.

Change in clinical disease after G85R knockdown

Transgenic Onset Early
phase
Late
phase
Disease
duration
Survival
G85Rflox/Cre-ER™ 14.8% 77.1% 57.6% 68.6% 19.6%
G85Rflox/Lhx3:Cre 14.6% 87.5% NS 46.6% 16.9%
G85Rflox/CD11b:Cre NS 58.8% 37.5% 43.2% 12.5%

Note: The numbers represent the per cent increase in the time to disease onset and increase in the duration of the early phase of disease, the late phase of disease, disease duration and survival compared to G85Rflox mice. The G85Rflox/Cre-ER™ mice were tamoxifen-treated. Data related to the knockdown in G85Rflox/Lhx:Cre mice (in which Cre is expressed in spinal and hindbrain MNs and a population of interneurons in the spinal cord) and G85Rflox/CD11b:Cre mice (in which Cre is expressed in microglia and activated macrophages) have been previously published (Wang et al. 2009b). NS=not statistically significant.

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