PubMed

Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degeneration.

Gregory-Evans K, Chang F, Hodges MD, Gregory-Evans CY.

Mol Vis. 2009 May 13;15:962-73.PMID: 19461934 [PubMed - indexed for MEDLINE]Related articlesFree article

Single choroideremia gene in nonmammalian vertebrates explains early embryonic lethality of the zebrafish model of choroideremia.

Moosajee M, Tulloch M, Baron RA, Gregory-Evans CY, Pereira-Leal JB, Seabra MC.

Invest Ophthalmol Vis Sci. 2009 Jun;50(6):3009-16. Epub 2008 Dec 30.PMID: 19117920 [PubMed - indexed for MEDLINE]Related articles

Translational bypass of nonsense mutations in zebrafish rep1, pax2.1 and lamb1 highlights a viable therapeutic option for untreatable genetic eye disease.

Moosajee M, Gregory-Evans K, Ellis CD, Seabra MC, Gregory-Evans CY.

Hum Mol Genet. 2008 Dec 15;17(24):3987-4000. Epub 2008 Sep 22.PMID: 18809619 [PubMed - indexed for MEDLINE]Related articles

Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa.

Guerin K, Gregory-Evans CY, Hodges MD, Moosajee M, Mackay DS, Gregory-Evans K, Flannery JG.

Exp Eye Res. 2008 Sep;87(3):197-207. Epub 2008 Jun 3.PMID: 18644591 [PubMed - indexed for MEDLINE]Related articles

SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.

Gregory-Evans CY, Moosajee M, Hodges MD, Mackay DS, Game L, Vargesson N, Bloch-Zupan A, Rüschendorf F, Santos-Pinto L, Wackens G, Gregory-Evans K.

Hum Mol Genet. 2007 Oct 15;16(20):2482-93. Epub 2007 Jul 25.PMID: 17656375 [PubMed - indexed for MEDLINE]Related articlesFree article

Ocular coloboma: a reassessment in the age of molecular neuroscience.

Gregory-Evans CY, Williams MJ, Halford S, Gregory-Evans K.

J Med Genet. 2004 Dec;41(12):881-91. Review.PMID: 15591273 [PubMed - indexed for MEDLINE]Related articlesFree article

Ocular coloboma and high myopia with Hirschsprung disease associated with a novel ZFHX1B missense mutation and trisomy 21.

Gregory-Evans CY, Vieira H, Dalton R, Adams GG, Salt A, Gregory-Evans K.

Am J Med Genet A. 2004 Nov 15;131(1):86-90.PMID: 15384097 [PubMed - indexed for MEDLINE]Related articles

Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

Toomes C, Bottomley HM, Jackson RM, Towns KV, Scott S, Mackey DA, Craig JE, Jiang L, Yang Z, Trembath R, Woodruff G, Gregory-Evans CY, Gregory-Evans K, Parker MJ, Black GC, Downey LM, Zhang K, Inglehearn CF.

Am J Hum Genet. 2004 Apr;74(4):721-30. Epub 2004 Mar 11.PMID: 15024691 [PubMed - indexed for MEDLINE]Related articlesFree article

Sorsby fundus dystrophy presenting with choroidal neovascularisation showing good response to steroid treatment.

Atan D, Gregory Evans CY, Louis D, Downes SM.

Br J Ophthalmol. 2004 Mar;88(3):440-1. No abstract available. PMID: 14977790 [PubMed - indexed for MEDLINE]Related articlesFree article

Transcriptional regulation and expression of the dominant drusen gene FBLN3 (EFEMP1) in mammalian retina.

Blackburn J, Tarttelin EE, Gregory-Evans CY, Moosajee M, Gregory-Evans K.

Invest Ophthalmol Vis Sci. 2003 Nov;44(11):4613-21.PMID: 14578376 [PubMed - indexed for MEDLINE]Related articlesFree article

Gene structure and tissue expression of human selenoprotein W, SEPW1, and identification of a retroprocessed pseudogene, SEPW1P.

Bellingham J, Gregory-Evans K, Fox MF, Gregory-Evans CY.

Biochim Biophys Acta. 2003 Jun 19;1627(2-3):140-6.PMID: 12818432 [PubMed - indexed for MEDLINE]Related articles

Successful photodynamic therapy for subretinal neovascularisation due to Sorsby's fundus dystrophy: 1 year follow up.

Wong SC, Fong KC, Lee N, Gregory-Evans K, Gregory-Evans CY.

Br J Ophthalmol. 2003 Jun;87(6):796-7. No abstract available. PMID: 12770993 [PubMed - indexed for MEDLINE]Related articlesFree article

Expression of opsin genes early in ocular development of humans and mice.

Tarttelin EE, Bellingham J, Bibb LC, Foster RG, Hankins MW, Gregory-Evans K, Gregory-Evans CY, Wells DJ, Lucas RJ.

Exp Eye Res. 2003 Mar;76(3):393-6.PMID: 12573668 [PubMed - indexed for MEDLINE]Related articles

Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouse.

Hodges MD, Vieira H, Gregory-Evans K, Gregory-Evans CY.

Genomics. 2002 Nov;80(5):531-42.PMID: 12408971 [PubMed - indexed for MEDLINE]Related articles

First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.

Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY.

Invest Ophthalmol Vis Sci. 2002 Aug;43(8):2540-5.PMID: 12147582 [PubMed - indexed for MEDLINE]Related articlesFree article

De novo mutations in the 5' regulatory region of the Norrie disease gene in retinopathy of prematurity.

Talks SJ, Ebenezer N, Hykin P, Adams G, Yang F, Schulenberg E, Gregory-Evans K, Gregory-Evans CY.

J Med Genet. 2001 Dec;38(12):E46. No abstract available. PMID: 11748312 [PubMed - indexed for MEDLINE]Related articlesFree article

Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development.

Bibb LC, Holt JK, Tarttelin EE, Hodges MD, Gregory-Evans K, Rutherford A, Lucas RJ, Sowden JC, Gregory-Evans CY.

Hum Mol Genet. 2001 Jul 15;10(15):1571-9.PMID: 11468275 [PubMed - indexed for MEDLINE]Related articlesFree article

Assignment of BCL2L11 to human chromosome band 2p13 with somatic cell and radiation hybrids.

Murray S, Halford S, Ebenezer ND, Gregory-Evans CY, Bhattacharya SS.

Cytogenet Cell Genet. 2001;92(3-4):353. No abstract available. PMID: 11435715 [PubMed - indexed for MEDLINE]Related articles

Molecular genetic heterogeneity in autosomal dominant drusen.

Tarttelin EE, Gregory-Evans CY, Bird AC, Weleber RG, Klein ML, Blackburn J, Gregory-Evans K.

J Med Genet. 2001 Jun;38(6):381-4.PMID: 11389162 [PubMed - indexed for MEDLINE]Related articlesFree article

Chromosomal mapping, gene structure and characterization of the human and murine RAB27B gene.

Ramalho JS, Tolmachova T, Hume AN, McGuigan A, Gregory-Evans CY, Huxley C, Seabra MC.

BMC Genet. 2001;2:2. Epub 2001 Feb 2.PMID: 11178108 [PubMed - indexed for MEDLINE]Related articlesFree article

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclase.

Gregory-Evans K, Kelsell RE, Gregory-Evans CY, Downes SM, Fitzke FW, Holder GE, Simunovic M, Mollon JD, Taylor R, Hunt DM, Bird AC, Moore AT.

Ophthalmology. 2000 Jan;107(1):55-61.PMID: 10647719 [PubMed - indexed for MEDLINE]Related articles

Cloning and characterization of a novel orphan G-protein-coupled receptor localized to human chromosome 2p16.

Tarttelin EE, Kirschner LS, Bellingham J, Baffi J, Taymans SE, Gregory-Evans K, Csaky K, Stratakis CA, Gregory-Evans CY.

Biochem Biophys Res Commun. 1999 Jun 24;260(1):174-80.PMID: 10381362 [PubMed - indexed for MEDLINE]Related articles

Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD).

Kermani S, Gregory-Evans K, Tarttelin EE, Bellingham J, Plant C, Bird AC, Fox M, Bhattacharya SS, Gregory-Evans CY.

Hum Genet. 1999 Jan;104(1):77-82.PMID: 10071196 [PubMed - indexed for MEDLINE]Related articles

Sequence and tissue expression of a novel human carbonic anhydrase-related protein, CARP-2, mapping to chromosome 19q13.3.

Bellingham J, Gregory-Evans K, Gregory-Evans CY.

Biochem Biophys Res Commun. 1998 Dec 18;253(2):364-7.PMID: 9878543 [PubMed - indexed for MEDLINE]Related articles

Abnormal cone synapses in human cone-rod dystrophy.

Gregory-Evans K, Fariss RN, Possin DE, Gregory-Evans CY, Milam AH.

Ophthalmology. 1998 Dec;105(12):2306-12.PMID: 9855164 [PubMed - indexed for MEDLINE]Related articles

Mapping of human interferon regulatory factor 3 (IRF3) to chromosome 19q13.3-13.4 by an intragenic polymorphic marker.

Bellingham J, Gregory-Evans K, Gregory-Evans CY.

Ann Hum Genet. 1998 May;62(Pt 3):231-4.PMID: 9803267 [PubMed - indexed for MEDLINE]Related articles

Microsatellite markers for the cone-rod retinal dystrophy gene, CRX, on 19q13.3.

Bellingham J, Gregory-Evans CY, Gregory-Evans K.

J Med Genet. 1998 Jun;35(6):527. No abstract available. PMID: 9643300 [PubMed - indexed for MEDLINE]Related articlesFree article

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q.

Kelsell RE, Gregory-Evans K, Gregory-Evans CY, Holder GE, Jay MR, Weber BH, Moore AT, Bird AC, Hunt DM.

Am J Hum Genet. 1998 Jul;63(1):274-9. No abstract available. PMID: 9634506 [PubMed - indexed for MEDLINE]Related articlesFree article

A polymorphic dinucleotide repeat in the 5' flanking region of the human interleukin 11 (IL11) gene.

Bellingham J, Gregory-Evans K, Gregory-Evans CY.

Immunogenetics. 1998 May;47(6):499-500. No abstract available. PMID: 9553159 [PubMed - indexed for MEDLINE]Related articles

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.

Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, Bellingham J, Ng D, Herbrick JA, Duncan A, Scherer SW, Tsui LC, Loutradis-Anagnostou A, Jacobson SG, Cepko CL, Bhattacharya SS, McInnes RR.

Cell. 1997 Nov 14;91(4):543-53.PMID: 9390563 [PubMed - indexed for MEDLINE]Related articles