Atypical Cadherins Celsr1-3 Differentially Regulate Migration of Facial Branchiomotor Neurons in MiceYibo Qu, Fadel Tissir, Derrick Glasco et al.|Journal of Neuroscience|2010Cited by 117
The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of DishevelledDerrick Glasco, Anand Chandrasekhar, W. Cully Bryant et al.|Developmental Biology|2012Cited by 54
Analysis of <scp>PRICKLE</scp>1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformationsTian Yang, Alexander G. Bassuk, Zhonglin Jia et al.|Molecular Genetics & Genomic Medicine|2013Cited by 38
The PCP protein Vangl2 regulates migration of hindbrain motor neurons by acting in floor plate cells, and independently of cilia functionVinoth Sittaramane, Anand Chandrasekhar, Xiufang Pan et al.|Developmental Biology|2013Cited by 27
The atypical cadherin Celsr1 functions non-cell autonomously to block rostral migration of facial branchiomotor neurons in miceDerrick Glasco, Anand Chandrasekhar, Whitney Pike et al.|Developmental Biology|2016Cited by 21