ARHGAP11B

Displaying 1 - 3 of 3 results tagged with this keyword.

Human-specific ARHGAP11B induces hallmarks of neocortical expansion in developing ferret neocortex

2019-01-09 (Publication)

A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification

2016-12-13 (Publication)

Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion.

2015-03-02 (Publication)