T. Keen

发表

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa.

A. Bird, M. Jay, F. Fitzke, 1992, Human molecular genetics.

Does isoform diversity explain functional differences in the 14-3-3 protein family?

R. Kleppe, T. Keen, E. Kjarland, 2006, Current pharmaceutical biotechnology.

Molecular genetic analysis of human inherited retinal degeneration

T. Keen, 1996 .

Cyclic AMP induces IPC leukemia cell apoptosis via CRE-and CDK-dependent Bim transcription

S. Døskeland, C. Kunick, R. Kleppe, 2011, Cell Death and Disease.

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

A. Bird, M. Jay, S. Bhattacharya, 1994, Human molecular genetics.

Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS gene.

A. Bird, F. Fitzke, H. Dollfus, 1995, Archives of ophthalmology.

Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow gene.

A. Bird, M. Jay, S. Bhattacharya, 1994, Ophthalmology.

Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities

C. Inglehearn, P. Reynolds, K. W. Brown, 1996, Genes, chromosomes & cancer.

Differential expression of particulate methane monooxygenase genes in the verrucomicrobial methanotroph ‘Methylacidiphilum kamchatkense’ Kam1

N. Birkeland, S. Jensen, T. Keen, 2012, Extremophiles.

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

A. Bird, M. Jay, C. Inglehearn, 1992, American journal of human genetics.

Regional assignment of 30 expressed sequence tags on human chromosome 7 using a somatic cell hybrid panel.

K. Grzeschik, C. Inglehearn, S. Bhattacharya, 1995, Genomics.

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

A. Bird, M. Jay, S. Bhattacharya, 1994, American journal of human genetics.

Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin gene.

A. Bird, C. Inglehearn, S. Bhattacharya, 1994, Human molecular genetics.

Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate

S. Robertson, C. Inglehearn, A. Mighell, 2002, European Journal of Human Genetics.

A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2–24.2.

M. Mohamed, C. Inglehearn, E. Sheridan, 2004, Journal of Medical Genetics.

Analysis of a human gene homologous to rat ventral prostate.1 protein.

C. Inglehearn, T. Keen, R. Peacock, 1997, Genomics.

A new family linked to the RP1 dominant retinitis pigmentosa locus on chromosome 8q

C. Inglehearn, H. Skirton, P. Lunt, 1999, Journal of medical genetics.

A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p.

J. Weissenbach, R. White, A. Cunningham, 1995, Genomics.

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

A. Bird, M. Jay, S. Bhattacharya, 1993, Nature Genetics.

PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factor.

S. Iguchi-Ariga, H. Ariga, C. Inglehearn, 2004, Experimental cell research.

Mutations and polymorphisms in the human peripherin‐RDS gene and their involvement in inherited retinal degeneration

C. Inglehearn, T. Keen, 1996, Human mutation.

Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36

M. Mohamed, M. McKibbin, C. Inglehearn, 2003, European Journal of Human Genetics.

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.

M. Hims, D. Hunt, T. Rosenberg, 2002, Human molecular genetics.

Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families.

C. Inglehearn, A. Morris, T. Keen, 1997, Journal of medical genetics.

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

M. Hims, D. Mackey, A. Bird, 2002, European Journal of Human Genetics.

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

D. Mackey, F. Cremers, A. Bird, 2001, Human molecular genetics.

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

A. Bird, A. Moore, C. Inglehearn, 1998, Journal of medical genetics.

Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosa.

M. Jay, S. Bhattacharya, F. Fitzke, 1994, The British journal of ophthalmology.

A new dominant retin : pigmentosa family mapping to the RP 18 1 on chromosome lqll

A. Moore, S. Bhattacharya, T. Keen, 2022 .

Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site.

A. Bird, M. Jay, S. Bhattacharya, 1994, The British journal of ophthalmology.

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

A. Bird, M. Jay, S. Bhattacharya, 1991, Genomics.

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

C. M. Kemp, A. Bird, S. Bhattacharya, 1992, The British journal of ophthalmology.

Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.

A. Bird, M. Jay, S. Bhattacharya, 1993, The British journal of ophthalmology.

A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13.

T J Keen, C. Inglehearn, L M Downey, 2001, American journal of human genetics.

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

A. Bird, M. Jay, C. Inglehearn, 1992, Genomics.