Detalhe da pesquisa
1.
Identification and validation of DOCK4 as a potential biomarker for risk of bone metastasis development in patients with early breast cancer.
J Pathol
; 247(3): 381-391, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30426503
2.
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism.
Am J Hum Genet
; 93(6): 1143-50, 2013 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24290379
3.
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Am J Hum Genet
; 89(3): 464-73, 2011 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-21907015
4.
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.
Vet Ophthalmol
; 17(2): 113-9, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23701506
5.
Toward routine use of 3D histopathology as a research tool.
Am J Pathol
; 180(5): 1835-42, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22490922
6.
Null mutations in LTBP2 cause primary congenital glaucoma.
Am J Hum Genet
; 84(5): 664-71, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19361779
7.
Past and current asbestos exposure and future mesothelioma risks in Britain: The Inhaled Particles Study (TIPS).
Int J Epidemiol
; 47(6): 1745-1756, 2018 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29534192
8.
Deregulation of IGF-binding proteins -2 and -5 contributes to the development of endocrine resistant breast cancer in vitro.
Oncotarget
; 7(22): 32129-43, 2016 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-27050076
9.
Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa.
Invest Ophthalmol Vis Sci
; 52(10): 7432-40, 2011 Sep 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-21862650
10.
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).
Nat Genet
; 43(12): 1189-92, 2011 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-22101682