Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comment
. 2013 Jan 25;288(4):2905.
doi: 10.1074/jbc.L112.439489.

RYK is not mutated in autosomal dominant Robinow syndrome

Comment

RYK is not mutated in autosomal dominant Robinow syndrome

Juliana F Mazzeu. J Biol Chem. .
No abstract available

PubMed Disclaimer

Comment in

Comment on

References

    1. Andre P., Wang Q., Wang N., Gao B., Schilit A., Halford M. M., Stacker S. A., Zhang X., Yang Y. (2012) The Wnt coreceptor Ryk regulates Wnt/planar cell polarity by modulating the degradation of the core planar cell polarity component Vangl2. J. Biol. Chem. 287, 44518–44525 - PMC - PubMed
    1. Person A. D., Beiraghi S., Sieben C. M., Hermanson S., Neumann A. N., Robu M. E., Schleiffarth J. R., Billington C. J., Jr., van Bokhoven H., Hoogeboom J. M., Mazzeu J. F., Petryk A., Schimmenti L. A., Brunner H. G., Ekker S. C., Lohr J. L. (2010) WNT5a mutations in patients with autosomal dominant Robinow syndrome. Dev. Dyn. 239, 327–337 - PMC - PubMed
    1. Halford M. M., Armes J., Buchert M., Meskenaite V., Grail D., Hibbs M. L., Wilks A. F., Farlie P. G., Newgreen D. F., Hovens C. M., Stacker S. A. (2000) Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk. Nat. Genet. 25, 414–418 - PubMed

LinkOut - more resources