Literature DB >> 16957474

Patient with an EYA1 mutation with features of branchio-oto-renal and oto-facio-cervical syndrome.

Catherine Mercer1, Rodney Gilbert, Sam Loughlin, Nicola Foulds.   

Abstract

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Year:  2006        PMID： 16957474     DOI： 10.1097/01.mcd.0000204986.54366.7c

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  3 in total

1.  HERV-mediated genomic rearrangement of EYA1 in an individual with branchio-oto-renal syndrome.

Authors:  Amarilis Sanchez-Valle; Xueqing Wang; Lorraine Potocki; Zhilian Xia; Sung-Hae L Kang; Mary E Carlin; Donnice Michel; Patricia Williams; Gerardo Cabrera-Meza; Ellen K Brundage; Anna L Eifert; Pawel Stankiewicz; Sau Wai Cheung; Seema R Lalani
Journal:  Am J Med Genet A       Date:  2010-11       Impact factor: 2.802

Review 2.  The Eyes Absent proteins in development and disease.

Authors:  Emmanuel Tadjuidje; Rashmi S Hegde
Journal:  Cell Mol Life Sci       Date:  2012-09-13       Impact factor: 9.261

3.  Eya3 promotes breast tumor-associated immune suppression via threonine phosphatase-mediated PD-L1 upregulation.

Authors:  Rebecca L Vartuli; Hengbo Zhou; Lingdi Zhang; Rani K Powers; Jared Klarquist; Pratyaydipta Rudra; Melanie Y Vincent; Debashis Ghosh; James C Costello; Ross M Kedl; Jill E Slansky; Rui Zhao; Heide L Ford
Journal:  J Clin Invest       Date:  2018-05-14       Impact factor: 14.808
  3 in total

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