Found: 11
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The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesis.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 11, p. 2251, doi. 10.1093/hmg/ddq104
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- Article
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.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 10, p. 1719, doi. 10.1093/hmg/ddp075
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- Article
Brainstem Respiratory Oscillators Develop Independently of Neuronal Migration Defects in the Wnt/PCP Mouse Mutant looptail.
- Published in:
- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0031140
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- Article
Atypical Cadherins Celsr1-3 Differentially Regulate Migration of Facial Branchiomotor Neurons in Mice.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 28, p. 9392, doi. 10.1523/JNEUROSCI.0124-10.2010
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- Article
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates.
- Published in:
- Nature Genetics, 2005, v. 37, n. 10, p. 1135, doi. 10.1038/ng1644
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- Article
Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator.
- Published in:
- Nature Genetics, 2001, v. 29, n. 4, p. 469, doi. 10.1038/ng768
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- Article
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 2, p. 87, doi. 10.1093/hmg/ddg014
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- Article
Severe neural tube defects inthe loop-tailmouse result from mutation of Lpp1,a novel gene involved in floor plate specification.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 22, p. 2593, doi. 10.1093/hmg/10.22.2593
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- Article
Retinal axon misrouting at the optic chiasm in mice with neural tube closure defects.
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- Genesis: The Journal of Genetics & Development, 2000, v. 27, n. 1, p. 32, doi. 10.1002/1526-968X(200005)27:1<32::AID-GENE50>3.0.CO;2-T
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- Article
THE GENETIC BASIS OF MAMMALIAN NEURULATION.
- Published in:
- Nature Reviews Genetics, 2003, v. 4, n. 10, p. 784, doi. 10.1038/nrg1181
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- Article
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.
- Published in:
- BMC Developmental Biology, 2010, v. 10, p. 87, doi. 10.1186/1471-213X-10-87
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- Article