Publications by authors named "Mike Shires"

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Identification and validation of DOCK4 as a potential biomarker for risk of bone metastasis development in patients with early breast cancer.
Jules A Westbrook, Steven L Wood, David A Cairns, Kathryn McMahon, Renu Gahlaut, Mike Shires

J Pathol· March 2019

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Past and current asbestos exposure and future mesothelioma risks in Britain: The Inhaled Particles Study (TIPS).
Clare Gilham, Christine Rake, John Hodgson, Andrew Darnton, Garry Burdett, Mike Shires

Int J Epidemiol· December 2018

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Deregulation of IGF-binding proteins -2 and -5 contributes to the development of endocrine resistant breast cancer in vitro.
Yousef Hawsawi, Matthew P Humphries, Alexander Wright, Angelene Berwick, Mike Shires

Oncotarget· May 2016

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Spectral domain optical coherence tomography imaging of the posterior segment of the eye in the retinal dysplasia and degeneration chicken, an animal model of inherited retinal degeneration.
Martin McKibbin, Manir Ali, Chris Inglehearn, Mike Shires, Kenny Boyle

Vet Ophthalmol· March 2014

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Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism.
James A Poulter, Musallam Al-Araimi, Ivan Conte, Maria M van Genderen, Eamonn Sheridan, Mike Shires

Am J Hum Genet· December 2013

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Toward routine use of 3D histopathology as a research tool.
Nicholas Roberts, Derek Magee, Yi Song, Keeran Brabazon, Mike Shires

Am J Pathol· May 2012

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Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).
Clare V Logan, Barbara Lucke, Caroline Pottinger, Zakia A Abdelhamed, David A Parry, Mike Shires

Nat Genet· November 2011

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Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa.
Manir Ali, Paul M Hocking, Martin McKibbin, Sorcha Finnegan, Mike Shires

Invest Ophthalmol Vis Sci· September 2011

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Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Kamron Khan, Adam Rudkin, David A Parry, Kathryn P Burdon, Martin McKibbin, Mike Shires

Am J Hum Genet· September 2011

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Null mutations in LTBP2 cause primary congenital glaucoma.
Manir Ali, Martin McKibbin, Adam Booth, David A Parry, Payal Jain, Mike Shires

Am J Hum Genet· May 2009

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