Članki z zahtevami za javni dostop - Stephanie HalfordVeč o tem
Na voljo nekje: 9
Detailed phenotypic and genotypic characterization of Bietti crystalline dystrophy
S Halford, G Liew, DS Mackay, PI Sergouniotis, R Holt, S Broadgate, ...
Ophthalmology 121 (6), 1174-1184, 2014
Zahteve: National Institute for Health Research, UK, Wellcome Trust
The hypothalamic photoreceptors regulating seasonal reproduction in birds: a prime role for VA opsin
JM García-Fernández, R Cernuda-Cernuda, WIL Davies, J Rodgers, ...
Frontiers in neuroendocrinology 37, 13-28, 2015
Zahteve: Australian Research Council, UK Biotechnology and Biological Sciences …
Mutations in the spliceosome component CWC27 cause retinal degeneration with or without additional developmental anomalies
M Xu, YA Xie, H Abouzeid, CT Gordon, A Fiorentino, Z Sun, A Lehman, ...
The American Journal of Human Genetics 100 (4), 592-604, 2017
Zahteve: US National Institutes of Health, National Natural Science Foundation of …
Isoforms of melanopsin mediate different behavioral responses to light
A Jagannath, S Hughes, A Abdelgany, CA Pothecary, S Di Pretoro, ...
Current Biology 25 (18), 2430-2434, 2015
Zahteve: UK Biotechnology and Biological Sciences Research Council, UK Medical …
Biallelic mutation of ARHGEF18, involved in the determination of epithelial apicobasal polarity, causes adult-onset retinal degeneration
G Arno, KJ Carss, S Hull, C Zihni, AG Robson, A Fiorentino, G Black, ...
The American Journal of Human Genetics 100 (2), 334-342, 2017
Zahteve: UK Biotechnology and Biological Sciences Research Council, UK Medical …
Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa
A Fiorentino, J Yu, G Arno, N Pontikos, S Halford, S Broadgate, ...
Molecular vision 24, 603, 2018
Zahteve: Cancer Research UK, UK Medical Research Council, National Institute for …
Characterization of CDH3-related congenital hypotrichosis with juvenile macular dystrophy
S Hull, G Arno, AG Robson, S Broadgate, V Plagnol, M McKibbin, ...
JAMA ophthalmology 134 (9), 992-1000, 2016
Zahteve: National Institute for Health Research, UK
Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapy
MS Singh, S Broadgate, R Mathur, R Holt, S Halford, RE MacLaren
Scientific reports 6, 23674, 2016
Zahteve: National Institute for Health Research, UK
Targeted deletion of an NRL- and CRX-regulated alternative promoter specifically silences FERM and PDZ domain containing 1 (Frmpd1) in rod photoreceptors
CK Campla, H Mast, L Dong, J Lei, S Halford, S Sekaran, A Swaroop
Human molecular genetics 28 (5), 804-817, 2018
Zahteve: US National Institutes of Health
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