The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled

Developmental Biology

Volumn 369, Issue 2, 2012, Pages 211-222

  Glasco, Derrick M ^a,h   Sittaramane, Vinoth ^a   Bryant, Whitney ^a   Fritzsch, Bernd ^b   Sawant, Anagha ^a   Paudyal, Anju ^c,d   Stewart, Michelle ^c   Andre, Philipp ^e   Cadete Vilhais Neto, Gonçalo ^f   Yang, Yingzi ^e   Song, Mi Ryoung ^g   Murdoch, Jennifer N ^c,d   Chandrasekhar, Anand ^a  

^a UNIVERSITY OF MISSOURI   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c MEDICAL RESEARCH COUNCIL   (United Kingdom)

^d UNIVERSITY OF LONDON   (United Kingdom)

^e NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^f UNIVERSITÉ DE STRASBOURG   (France)

^g Gwangju Institute of Science and Technology (GIST)   (South Korea)

^h Bob Jones University   (United States)

Author keywords

Disheveled; Facial branchiomotor neuron migration; Looptail; Planar Cell Polarity signaling; Protein tyrosine kinase 7; Van Gogh like 2

Indexed keywords

DISHEVELLED PROTEIN; MEMBRANE PROTEIN; PROTEIN VANGL2; UNCLASSIFIED DRUG; WNT PROTEIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL MIGRATION; CELL TRANSFORMATION; CELL TYPE; CONTROLLED STUDY; DISEASE EXACERBATION; DISHEVELLED 1 GENE; DISHEVELLED 2 GENE; EMBRYO; EMBRYO CELL; FACIAL BRANCHIOMOTOR NEURON; GENE; GENE DISRUPTION; GENE FUNCTION; GENE INACTIVATION; GENE INTERACTION; GENE LOSS; MOTONEURON; MOUSE; MUTANT; NEURAL STEM CELL; NEURAL TUBE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; PTK7 GENE; RECEPTOR GENE; RHOMBENCEPHALON; RHOMBOMERE 4; RHOMBOMERE 6; SIGNAL TRANSDUCTION; VANGL2 GENE;

DANIO RERIO; VERTEBRATA;

EID: 84865176040     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2012.06.021     Document Type: Article

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