- A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial cleftingAdam P Ross
Department of Pathology and Laboratory Medicine, University of California Davis, Sacramento, California, United States of America
PLoS ONE 8:e69333. 2013..No deleterious variants in the PAK1IP1 gene coding region were recognized, however, we identified a borderline association effect for SNP rs494723 suggesting a possible role for the PAK1IP1 gene in human orofacial clefting. ..
- Meningeal defects alter the tangential migration of cortical interneurons in Foxc1hith/hith miceKonstantinos Zarbalis
Institute of Pediatric Regenerative Medicine Shriners Hospitals for Children, Northern California, 2425 Stockton Blvd, CA 95817, USA
Neural Dev 7:2. 2012..While a number of forebrain-expressed molecules regulating this process have emerged, it remains unclear to what extent structures outside the brain, like the forebrain meninges, are involved...