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. 2013 Sep 3;7:141. doi: 10.3389/fncel.2013.00141

Table 1.

Dicer-CKO phenotypes in the cortex and retina.

Cre transgene Cre expression Main phenotype Reference
Cortex
Foxg1-Cre From E8 in most forebrain cells Altered balance of apical and basal progenitors Nowakowski et al. (2011)
Emx1-Cre From E10 to E10.5 in most cells of the dorsal telencephalon Overproduction of early-born neurons and reduced number of Brn1-expressing upper-layer neurons Kawase-Koga et al. (2009)
Nestin-Cre From E10 to E10.5 in forebrain stem cells and progenitors Affected late-born neuron generation and migration De Pietri Tonelli et al. (2008)
CamKII-Cre From E15.5 in post-mitotic neurons of the cortex and hippocampus Normal layering; reduced dendritic branch elaboration Davis et al. (2008)
Retina
Chx10-Cre Mosaic pattern, from E14.5 in progenitors of all retinal layers Decreased ERG responses, retinal disorganization, progressive retinal degeneration from P16 Damiani et al. (2008)
αPax6-Cre Peripheral retina from day E10.5; differentiated amacrine cells, by E14.5 Overproduction of ganglion cells, failure to generate late cell types such as Müller glia and rod photoreceptors Georgi and Reh (2010)
Dkk3-Cre From E10.5 in progenitors of all neuroretinal cell types Microphthalmia, massive apoptosis Iida et al. (2011)
Rx-Cre Ubiquitously in the developing neuroretina and optic stalk; later in the optic chiasm Microphthalmia, massive apoptosis, defects in retinal ganglion cell axon pathfinding Pinter and Hindges (2010)