Lester D - Search Results

1

Retinitis pigmentosa and mutations in rhodopsin.

Bhattacharya S, Lester D, Keen J, Bashir R, Lauffart B, Inglehearn CF, Jay M, Bird AC. Bhattacharya S, et al. Among authors: lester d. Lancet. 1991 Jan 19;337(8734):185. doi: 10.1016/0140-6736(91)90858-m. Lancet. 1991. PMID: 1670831 No abstract available.

2

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.

3

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

4

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.

5

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

6

Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity.

Lester DH, Inglehearn CF, Bashir R, Ackford H, Esakowitz L, Jay M, Bird AC, Wright AF, Papiha SS, Bhattacharya SS. Lester DH, et al. Am J Hum Genet. 1990 Sep;47(3):536-41. Am J Hum Genet. 1990. PMID: 2393026 Free PMC article.

7

Rapid detection of single base mismatches as heteroduplexes on Hydrolink gels.

Keen J, Lester D, Inglehearn C, Curtis A, Bhattacharya S. Keen J, et al. Among authors: lester d. Trends Genet. 1991 Jan;7(1):5. doi: 10.1016/0168-9525(91)90004-a. Trends Genet. 1991. PMID: 2003336 No abstract available.

8

Frequency of rhodopsin codon 23 mutation and retinitis pigmentosa.

Lester DH, Wright AF. Lester DH, et al. Lancet. 1991 Jun 29;337(8757):1609. doi: 10.1016/0140-6736(91)93307-u. Lancet. 1991. PMID: 1675737 No abstract available.

9

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.

10

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. Invest Ophthalmol Vis Sci. 2011 Sep 27;52(10):7432-40. doi: 10.1167/iovs.11-7872. Invest Ophthalmol Vis Sci. 2011. PMID: 21862650

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