|
1
|
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates.
|
Nat Genet
|
2005
|
4.76
|
|
2
|
The genetic basis of mammalian neurulation.
|
Nat Rev Genet
|
2003
|
4.14
|
|
3
|
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse.
|
Curr Biol
|
2003
|
3.31
|
|
4
|
Vangl2 acts via RhoA signaling to regulate polarized cell movements during development of the proximal outflow tract.
|
Circ Res
|
2005
|
2.13
|
|
5
|
Disruption of planar cell polarity signaling results in congenital heart defects and cardiomyopathy attributable to early cardiomyocyte disorganization.
|
Circ Res
|
2007
|
1.85
|
|
6
|
Non-cell-autonomous roles for the planar cell polarity gene Vangl2 in development of the coronary circulation.
|
Circ Res
|
2008
|
1.60
|
|
7
|
The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesis.
|
Hum Mol Genet
|
2010
|
1.30
|
|
8
|
Atypical cadherins Celsr1-3 differentially regulate migration of facial branchiomotor neurons in mice.
|
J Neurosci
|
2010
|
1.25
|
|
9
|
Epidermal wound repair is regulated by the planar cell polarity signaling pathway.
|
Dev Cell
|
2010
|
1.25
|
|
10
|
Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway.
|
Hum Mol Genet
|
2009
|
1.16
|
|
11
|
Secreted frizzled-related protein disrupts PCP in eye lens fiber cells that have polarised primary cilia.
|
Dev Biol
|
2009
|
1.08
|
|
12
|
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear.
|
BMC Dev Biol
|
2010
|
1.06
|
|
13
|
Scribble is required for normal epithelial cell-cell contacts and lumen morphogenesis in the mammalian lung.
|
Dev Biol
|
2012
|
1.01
|
|
14
|
The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled.
|
Dev Biol
|
2012
|
1.00
|
|
15
|
Dishevelled: linking convergent extension with neural tube closure.
|
Trends Neurosci
|
2003
|
0.96
|
|
16
|
Cloning and characterization of Igsf9 in mouse and human: a new member of the immunoglobulin superfamily expressed in the developing nervous system.
|
Genomics
|
2002
|
0.88
|
|
17
|
Brainstem respiratory oscillators develop independently of neuronal migration defects in the Wnt/PCP mouse mutant looptail.
|
PLoS One
|
2012
|
0.76
|