Inglehearn CF - Search Results

1

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

2

Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.

Moore AT, Fitzke FW, Kemp CM, Arden GB, Keen TJ, Inglehearn CF, Bhattacharya SS, Bird AC. Moore AT, et al. Among authors: inglehearn cf. Br J Ophthalmol. 1992 Aug;76(8):465-9. doi: 10.1136/bjo.76.8.465. Br J Ophthalmol. 1992. PMID: 1390527 Free PMC article.

3

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. Am J Hum Genet. 1992 Mar;50(3):590-7. Am J Hum Genet. 1992. PMID: 1539595 Free PMC article.

4

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: inglehearn cf. Lancet. 1991 Jan 19;337(8734):185. doi: 10.1016/0140-6736(91)90858-m. Lancet. 1991. PMID: 1670831 No abstract available.

5

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: inglehearn cf. Genomics. 1991 Sep;11(1):199-205. doi: 10.1016/0888-7543(91)90119-y. Genomics. 1991. PMID: 1765377

6

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. Am J Hum Genet. 1991 Jan;48(1):26-30. Am J Hum Genet. 1991. PMID: 1985460 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. Trends Genet. 1991 Jan;7(1):5. doi: 10.1016/0168-9525(91)90004-a. Trends Genet. 1991. PMID: 2003336 No abstract available.

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. Genomics. 1990 Jan;6(1):168-73. doi: 10.1016/0888-7543(90)90462-4. Genomics. 1990. PMID: 2303257

9

Better fingerprinting with PCR.

Bellamy R, Inglehearn C, Lester D, Hardcastle A, Bhattacharya S. Bellamy R, et al. Trends Genet. 1990 Feb;6(2):32. doi: 10.1016/0168-9525(90)90054-a. Trends Genet. 1990. PMID: 2336717 No abstract available.

10

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. Among authors: inglehearn cf. Am J Hum Genet. 1990 Sep;47(3):536-41. Am J Hum Genet. 1990. PMID: 2393026 Free PMC article.

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