Tarttelin EE - Search Results

1

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.

2

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. Blackburn J, et al. Among authors: tarttelin ee. Invest Ophthalmol Vis Sci. 2003 Nov;44(11):4613-21. doi: 10.1167/iovs.03-0112. Invest Ophthalmol Vis Sci. 2003. PMID: 14578376

3

A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p.

Tarttelin EE, Plant C, Weissenbach J, Bird AC, Bhattacharya SS, Inglehearn CF. Tarttelin EE, et al. J Med Genet. 1996 Jun;33(6):518-20. doi: 10.1136/jmg.33.6.518. J Med Genet. 1996. PMID: 8782056 Free PMC article.

4

A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity.

Inglehearn CF, Tarttelin EE, Plant C, Peacock RE, al-Maghtheh M, Vithana E, Bird AC, Bhattacharya SS. Inglehearn CF, et al. Among authors: tarttelin ee. J Med Genet. 1998 Jan;35(1):1-5. doi: 10.1136/jmg.35.1.1. J Med Genet. 1998. PMID: 9475085 Free PMC article.

5

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. Among authors: tarttelin ee. Hum Genet. 1999 Jan;104(1):77-82. doi: 10.1007/s004390050913. Hum Genet. 1999. PMID: 10071196

6

A new dominant retinitis pigmentosa family mapping to the RP18 locus on chromosome 1q11-21.

Inglehearn CF, Tarttelin EE, Keen TJ, Bhattacharya SS, Moore AT, Taylor R, Bird AC. Inglehearn CF, et al. Among authors: tarttelin ee. J Med Genet. 1998 Sep;35(9):788-9. doi: 10.1136/jmg.35.9.788. J Med Genet. 1998. PMID: 9733043 Free PMC article. No abstract available.

7

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

8

Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

McKie AB, McHale JC, Keen TJ, Tarttelin EE, Goliath R, van Lith-Verhoeven JJ, Greenberg J, Ramesar RS, Hoyng CB, Cremers FP, Mackey DA, Bhattacharya SS, Bird AC, Markham AF, Inglehearn CF. McKie AB, et al. Among authors: tarttelin ee. Hum Mol Genet. 2001 Jul 15;10(15):1555-62. doi: 10.1093/hmg/10.15.1555. Hum Mol Genet. 2001. PMID: 11468273

9

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. Bibb LC, et al. Among authors: tarttelin ee. Hum Mol Genet. 2001 Jul 15;10(15):1571-9. doi: 10.1093/hmg/10.15.1571. Hum Mol Genet. 2001. PMID: 11468275

10

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. Tarttelin EE, et al. Exp Eye Res. 2003 Mar;76(3):393-6. doi: 10.1016/s0014-4835(02)00300-7. Exp Eye Res. 2003. PMID: 12573668

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