Inglehearn CF - Search Results

1

Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosa.

Ivings L, Towns KV, Matin MA, Taylor C, Ponchel F, Grainger RJ, Ramesar RS, Mackey DA, Inglehearn CF. Ivings L, et al. Among authors: inglehearn cf. Mol Vis. 2008;14:2357-66. Epub 2008 Dec 18. Mol Vis. 2008. PMID: 19096719 Free PMC article.

2

Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: further locus heterogeneity in adRP.

Bashir R, Inglehearn CF, Keen TJ, Lindsey J, Atif U, Carter SA, Stephenson AM, Jackson A, Jay M, Bird AC, et al. Bashir R, et al. Among authors: inglehearn cf. Genomics. 1992 Sep;14(1):191-3. doi: 10.1016/s0888-7543(05)80306-4. Genomics. 1992. PMID: 1427827

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

4

New strategies in molecular genetic studies of X-linked retinitis pigmentosa.

Jay M, Inglehearn C. Jay M, et al. Eye (Lond). 1990;4 ( Pt 5):737-42. doi: 10.1038/eye.1990.105. Eye (Lond). 1990. PMID: 1980893

5

An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q.

Bardien S, Ebenezer N, Greenberg J, Inglehearn CF, Bartmann L, Goliath R, Beighton P, Ramesar R, Bhattacharya SS. Bardien S, et al. Among authors: inglehearn cf. Hum Mol Genet. 1995 Aug;4(8):1459-62. doi: 10.1093/hmg/4.8.1459. Hum Mol Genet. 1995. PMID: 7581389

6

Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19.

al-Maghtheh M, Inglehearn CF, Keen TJ, Evans K, Moore AT, Jay M, Bird AC, Bhattacharya SS. al-Maghtheh M, et al. Among authors: inglehearn cf. Hum Mol Genet. 1994 Feb;3(2):351-4. doi: 10.1093/hmg/3.2.351. Hum Mol Genet. 1994. PMID: 8004108

7

Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9).

Inglehearn CF, Keen TJ, al-Maghtheh M, Gregory CY, Jay MR, Moore AT, Bird AC, Bhattacharya SS. Inglehearn CF, et al. Am J Hum Genet. 1994 Apr;54(4):675-80. Am J Hum Genet. 1994. PMID: 8128965 Free PMC article.

8

A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa family.

al-Maghtheh M, Kim RY, Hardcastle A, Inglehearn C, Bhattacharya SS. al-Maghtheh M, et al. Hum Mol Genet. 1994 Jan;3(1):205-6. doi: 10.1093/hmg/3.1.205. Hum Mol Genet. 1994. PMID: 8162031 No abstract available.

9

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

Inglehearn CF, Carter SA, Keen TJ, Lindsey J, Stephenson AM, Bashir R, al-Maghtheh M, Moore AT, Jay M, Bird AC, et al. Inglehearn CF, et al. Nat Genet. 1993 May;4(1):51-3. doi: 10.1038/ng0593-51. Nat Genet. 1993. PMID: 8513323

10

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. Among authors: inglehearn cf. 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.

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