Lester DH - Search Results

1

Mutation in the guanine nucleotide-binding protein beta-3 causes retinal degeneration and embryonic mortality in chickens.

Tummala H, Ali M, Getty P, Hocking PM, Burt DW, Inglehearn CF, Lester DH. Tummala H, et al. Among authors: lester dh. Invest Ophthalmol Vis Sci. 2006 Nov;47(11):4714-8. doi: 10.1167/iovs.06-0292. Invest Ophthalmol Vis Sci. 2006. PMID: 17065478

2

Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa.

Ali M, Hocking PM, McKibbin M, Finnegan S, Shires M, Poulter JA, Prescott K, Booth A, Raashid Y, Jafri H, Ruddle JB, Mackey DA, Jacobson SG, Toomes C, Lester DH, Burt DW, Curry WJ, Inglehearn CF. Ali M, et al. Among authors: lester dh. Invest Ophthalmol Vis Sci. 2011 Sep 27;52(10):7432-40. doi: 10.1167/iovs.11-7872. Invest Ophthalmol Vis Sci. 2011. PMID: 21862650

3

The D153del mutation in GNB3 gene causes tissue specific signalling patterns and an abnormal renal morphology in Rge chickens.

Tummala H, Fleming S, Hocking PM, Wehner D, Naseem Z, Ali M, Inglehearn CF, Zhelev N, Lester DH. Tummala H, et al. Among authors: lester dh. PLoS One. 2011;6(8):e21156. doi: 10.1371/journal.pone.0021156. Epub 2011 Aug 22. PLoS One. 2011. PMID: 21887213 Free PMC article.

4

Genetic, ophthalmic, morphometric and histopathological analysis of the Retinopathy Globe Enlarged (rge) chicken.

Inglehearn CF, Morrice DR, Lester DH, Robertson GW, Mohamed MD, Simmons I, Downey LM, Thaung C, Bridges LR, Paton IR, Smith J, Petersen-Jones S, Hocking PM, Burt DW. Inglehearn CF, et al. Among authors: lester dh. Mol Vis. 2003 Jul 1;9:295-300. Mol Vis. 2003. PMID: 12847422 Free article.

5

Correction of the Pathogenic Alternative Splicing, Caused by the Common GNB3 c.825C>T Allele, Using a Novel, Antisense Morpholino.

McGlinchey JC, Tummala H, Lester DH. McGlinchey JC, et al. Among authors: lester dh. Nucleic Acid Ther. 2016 Aug;26(4):257-65. doi: 10.1089/nat.2015.0571. Epub 2016 Mar 30. Nucleic Acid Ther. 2016. PMID: 27028457

6

Analysis of the rdd locus in chicken: a model for human retinitis pigmentosa.

Burt DW, Morrice DR, Lester DH, Robertson GW, Mohamed MD, Simmons I, Downey LM, Thaung C, Bridges LR, Paton IR, Gentle M, Smith J, Hocking PM, Inglehearn CF. Burt DW, et al. Among authors: lester dh. Mol Vis. 2003 Apr 30;9:164-70. Mol Vis. 2003. PMID: 12724645 Free article.

7

Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site.

Keen TJ, Inglehearn CF, Lester DH, Bashir R, Jay M, Bird AC, Jay B, Bhattacharya SS. Keen TJ, et al. Among authors: lester dh. Genomics. 1991 Sep;11(1):199-205. doi: 10.1016/0888-7543(91)90119-y. Genomics. 1991. PMID: 1765377

8

No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity.

Inglehearn CF, Jay M, Lester DH, Bashir R, Jay B, Bird AC, Wright AF, Evans HJ, Papiha SS, Bhattacharya SS. Inglehearn CF, et al. Among authors: lester dh. Genomics. 1990 Jan;6(1):168-73. doi: 10.1016/0888-7543(90)90462-4. Genomics. 1990. PMID: 2303257

9

Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families.

Inglehearn CF, Lester DH, Bashir R, Atif U, Keen TJ, Sertedaki A, Lindsey J, Jay M, Bird AC, Farrar GJ, et al. Inglehearn CF, et al. Among authors: lester dh. Am J Hum Genet. 1992 Mar;50(3):590-7. Am J Hum Genet. 1992. PMID: 1539595 Free PMC article.

10

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.

Inglehearn CF, Bashir R, Lester DH, Jay M, Bird AC, Bhattacharya SS. Inglehearn CF, et al. Among authors: lester dh. Am J Hum Genet. 1991 Jan;48(1):26-30. Am J Hum Genet. 1991. PMID: 1985460 Free PMC article.

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