Cheryl Gregory-Evans
Cheryl Gregory-Evans
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Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
CL Freund, CY Gregory-Evans, T Furukawa, M Papaioannou, J Looser, ...
Cell 91 (4), 543-553, 1997
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q
C Toomes, HM Bottomley, RM Jackson, KV Towns, S Scott, DA Mackey, ...
The American Journal of Human Genetics 74 (4), 721-730, 2004
Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy
RE Kelsell, K Gregory-Evans, AM Payne, I Perrault, J Kaplan, RB Yang, ...
Human molecular genetics 7 (7), 1179-1184, 1998
Ocular coloboma: a reassessment in the age of molecular neuroscience
CY Gregory-Evans, MJ Williams, S Halford, K Gregory-Evans
Journal of medical genetics 41 (12), 881-891, 2004
Retinoblastoma has properties of a cone precursor tumor and depends upon cone-specific MDM2 signaling
XL Xu, Y Fang, TC Lee, D Forrest, C Gregory-Evans, D Almeida, A Liu, ...
Cell 137 (6), 1018-1031, 2009
Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion.
BSS Evans K, Fryer A, Inglehearn C, Duvall-Young J, Whittaker J, Gregory CY ...
Nature Genetics 6, 210-213, 1994
Focused magnetic stem cell targeting to the retina using superparamagnetic iron oxide nanoparticles
A Yanai, UO Häfeli, AL Metcalfe, P Soema, L Addo, CY Gregory-Evans, ...
Cell transplantation 21 (6), 1137-1148, 2012
Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development.
LC Bibb, JKL Holt, EE Tarttelin, MD Hodges, K Gregory-Evans, ...
Human Molecular Genetics 10 (15), 1571-1579, 2001
Autosomal dominant cone–rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase
K Gregory-Evans, RE Kelsell, CY Gregory-Evans, SM Downes, FW Fitzke, ...
Ophthalmology 107 (1), 55-61, 2000
Postnatal manipulation of Pax6 dosage reverses congenital tissue malformation defects
CY Gregory-Evans, X Wang, KM Wasan, J Zhao, AL Metcalfe, ...
The Journal of clinical investigation 124 (1), 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype
I Filges, E Nosova, E Bruder, S Tercanli, K Townsend, WT Gibson, ...
Clinical genetics 86 (3), 220-228, 2014
Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
BSS Al-Maghtheh M, Gregory C, Inglehearn C, Hardcastle A
Hum Mutat 2, 249-255, 1993
Rhodospin mutations in autosomal dominant retinitis pigmentosa.
BSS Al-Maghtheh M, Gregory C, Inglehearn C, Hardcastle A
Human Mutation 2, 249-255, 1993
Expression of opsin genes early in ocular development of humans and mice
EE Tarttelin, J Bellingham, LC Bibb, RG Foster, MW Hankins, ...
Experimental eye research 76 (3), 393-396, 2003
RANTES stimulates Ca2+ mobilization and inositol trisphosphate (IP3) formation in cells transfected with G protein‐coupled receptor 75
A Ignatov, J Robert, C Gregory‐Evans, HC Schaller
British journal of pharmacology 149 (5), 490-497, 2006
Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q.
RE Kelsell, K Gregory-Evans, CY Gregory-Evans, GE Holder, MR Jay, ...
American journal of human genetics 63 (1), 274, 1998
Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degeneration
K Gregory-Evans, F Chang, MD Hodges, CY Gregory-Evans
Molecular vision 15, 962, 2009
The gene responsible for autosomal dominant Doyne’s honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.
BSS Gregory CY, Evans K, Wijesuriya SD, Kermani S, Jay MR, Plant C, Cox N ...
Hum Mol Genet 5, 1055-1059, 1996
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p.
HDM Kelsell RE, Evans K, Gregory CY, Moore AT, Bird AC
Hum Mol Genet 6, 597-600, 1997
Gene networks: dissecting pathways in retinal development and disease
CY Gregory-Evans, VA Wallace, K Gregory-Evans
Progress in retinal and eye research 33, 40-66, 2013
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