Literature DB >> 23355721

RYK is not mutated in autosomal dominant Robinow syndrome.

Juliana F Mazzeu.   

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Year:  2013        PMID： 23355721      PMCID： PMC3554954          DOI： 10.1074/jbc.L112.439489

Source DB:  PubMed          Journal:  J Biol Chem        ISSN： 0021-9258            Impact factor:   5.157


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  3 in total

1.  Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk.

Authors:  M M Halford; J Armes; M Buchert; V Meskenaite; D Grail; M L Hibbs; A F Wilks; P G Farlie; D F Newgreen; C M Hovens; S A Stacker
Journal:  Nat Genet       Date:  2000-08       Impact factor: 38.330

2.  The Wnt coreceptor Ryk regulates Wnt/planar cell polarity by modulating the degradation of the core planar cell polarity component Vangl2.

Authors:  Philipp Andre; Qianyi Wang; Na Wang; Bo Gao; Arielle Schilit; Michael M Halford; Steven A Stacker; Xuemin Zhang; Yingzi Yang
Journal:  J Biol Chem       Date:  2012-11-09       Impact factor: 5.157

3.  WNT5A mutations in patients with autosomal dominant Robinow syndrome.

Authors:  Anthony D Person; Soraya Beiraghi; Christine M Sieben; Spencer Hermanson; Ann N Neumann; Mara E Robu; J Robert Schleiffarth; Charles J Billington; Hans van Bokhoven; Jeannette M Hoogeboom; Juliana F Mazzeu; Anna Petryk; Lisa A Schimmenti; Han G Brunner; Stephen C Ekker; Jamie L Lohr
Journal:  Dev Dyn       Date:  2010-01       Impact factor: 3.780
  3 in total
  1 in total

1.  Reply to Mazzeu: Human mutations in RYK might cause Robinow syndrome.

Authors:  Philipp Andre; Yingzi Yang
Journal:  J Biol Chem       Date:  2013-01-25       Impact factor: 5.157
  1 in total

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