Gregory-Evans CY - Search Results

1

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. Gregory-Evans K, et al. Ophthalmology. 2000 Jan;107(1):55-61. doi: 10.1016/s0161-6420(99)00038-x. Ophthalmology. 2000. PMID: 10647719

2

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

Bellingham J, Gregory-Evans K, Gregory-Evans CY. Bellingham J, et al. Immunogenetics. 1998 May;47(6):499-500. doi: 10.1007/s002510050390. Immunogenetics. 1998. PMID: 9553159 No abstract available.

3

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. Kelsell RE, et al. Am J Hum Genet. 1998 Jul;63(1):274-9. doi: 10.1086/301905. Am J Hum Genet. 1998. PMID: 9634506 Free PMC article. No abstract available.

4

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

Bellingham J, Gregory-Evans CY, Gregory-Evans K. Bellingham J, et al. J Med Genet. 1998 Jun;35(6):527. doi: 10.1136/jmg.35.6.527. J Med Genet. 1998. PMID: 9643300 Free PMC article. No abstract available.

5

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. Bellingham J, et al. Ann Hum Genet. 1998 May;62(Pt 3):231-4. doi: 10.1046/j.1469-1809.1998.6230231.x. Ann Hum Genet. 1998. PMID: 9803267

6

Abnormal cone synapses in human cone-rod dystrophy.

Gregory-Evans K, Fariss RN, Possin DE, Gregory-Evans CY, Milam AH. Gregory-Evans K, et al. Ophthalmology. 1998 Dec;105(12):2306-12. doi: 10.1016/S0161-6420(98)91233-7. Ophthalmology. 1998. PMID: 9855164 Free article.

7

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. Bellingham J, et al. Biochem Biophys Res Commun. 1998 Dec 18;253(2):364-7. doi: 10.1006/bbrc.1998.9449. Biochem Biophys Res Commun. 1998. PMID: 9878543

8

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. Kermani S, et al. Hum Genet. 1999 Jan;104(1):77-82. doi: 10.1007/s004390050913. Hum Genet. 1999. PMID: 10071196

9

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. Tarttelin EE, et al. Biochem Biophys Res Commun. 1999 Jun 24;260(1):174-80. doi: 10.1006/bbrc.1999.0753. Biochem Biophys Res Commun. 1999. PMID: 10381362

10

Molecular genetic heterogeneity in autosomal dominant drusen.

Tarttelin EE, Gregory-Evans CY, Bird AC, Weleber RG, Klein ML, Blackburn J, Gregory-Evans K. Tarttelin EE, et al. J Med Genet. 2001 Jun;38(6):381-4. doi: 10.1136/jmg.38.6.381. J Med Genet. 2001. PMID: 11389162 Free PMC article.

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