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Results: 1-23 |
Results: 23
Comparison of CO2 stunning with manual electrical stunning (50 Hz) of pigson carcass and meat quality
Authors: Channon, HA Payne, AM Warner, RD
Citation: Ha. Channon et al., Comparison of CO2 stunning with manual electrical stunning (50 Hz) of pigson carcass and meat quality, MEAT SCI, 60(1), 2002, pp. 63-68
A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family
Authors: Hameed, A Khaliq, S Ismail, M Anwar, K Mehdi, SQ Bessant, D Payne, AM Bhattacharya, SS
Citation: A. Hameed et al., A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family, INV OPHTH V, 42(7), 2001, pp. 1436-1438
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies
Authors: Payne, AM Morris, AG Downes, SM Johnson, S Bird, AC Moore, AT Bhattacharya, SS Hunt, DM
Citation: Am. Payne et al., Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies, J MED GENET, 38(9), 2001, pp. 611-614
Spectrum of mutations in USH2A in British patients with Usher syndrome type II
Authors: Leroy, BP Aragon-Martin, JA Weston, MD Bessant, DAR Willis, C Webster, AR Bird, AC Kimberling, WJ Payne, AM Bhattacharya, SS
Citation: Bp. Leroy et al., Spectrum of mutations in USH2A in British patients with Usher syndrome type II, EXP EYE RES, 72(5), 2001, pp. 503-509
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1
Authors: Downes, SM Payne, AM Kelsell, RE Fitzke, FW Holder, GE Hunt, DM Moore, AT Bird, AC
Citation: Sm. Downes et al., Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1, ARCH OPHTH, 119(11), 2001, pp. 1667-1673
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1
Authors: Downes, SM Holder, GE Fitzke, FW Payne, AM Warren, MJ Bhattacharya, SS Bird, AC
Citation: Sm. Downes et al., Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1, ARCH OPHTH, 119(1), 2001, pp. 96-105
Prevalence of AIPL1 mutations in inherited retinal degenerative disease
Authors: Sohocki, MM Perrault, I Leroy, BP Payne, AM Dharmaraj, S Bhattacharya, SS Kaplan, J Maumenee, IH Koenekoop, R Meire, FM Birch, DG Heckenlively, JR Daiger, SP
Citation: Mm. Sohocki et al., Prevalence of AIPL1 mutations in inherited retinal degenerative disease, MOL GEN MET, 70(2), 2000, pp. 142-150
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenitalamaurosis
Authors: Sohocki, MM Bowne, SJ Sullivan, LS Blackshaw, S Cepko, CL Payne, AM Bhattacharya, SS Khaliq, S Mehdi, SQ Birch, DG Harrison, WR Elder, FFB Heckenlively, JR Daiger, SP
Citation: Mm. Sohocki et al., Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenitalamaurosis, NAT GENET, 24(1), 2000, pp. 79-83
NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies
Authors: Bessant, DAR Payne, AM Plant, C Bird, AC Swaroop, A Bhattacharya, SS
Citation: Dar. Bessant et al., NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies, EUR J HUM G, 8(10), 2000, pp. 783-787
Halothane genotype, pre-slaughter handling and stunning method all influence pork quality
Authors: Channon, HA Payne, AM Warner, RD
Citation: Ha. Channon et al., Halothane genotype, pre-slaughter handling and stunning method all influence pork quality, MEAT SCI, 56(3), 2000, pp. 291-299
A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13
Authors: Hameed, A Khaliq, S Ismail, M Anwar, K Ebenezer, ND Jordan, T Mehdi, SQ Payne, AM Bhattacharya, SS
Citation: A. Hameed et al., A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13, INV OPHTH V, 41(3), 2000, pp. 629-633
Novel locus for autosomal recessive cone-rod dystrophy CORDS mapping to chromosome 1q12-q24
Authors: Khaliq, S Hameed, A Ismail, M Anwar, K Leroy, BP Mehdi, SQ Payne, AM Bhattacharya, SS
Citation: S. Khaliq et al., Novel locus for autosomal recessive cone-rod dystrophy CORDS mapping to chromosome 1q12-q24, INV OPHTH V, 41(12), 2000, pp. 3709-3712
Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP 12) and mutation analysis of the candidate gene RGS16 (RGS-r)
Authors: Bessant, DAR Payne, AM Snow, BE Antinolo, G Mehdi, SQ Bird, AC Siderovski, DP Bhattacharya, SS
Citation: Dar. Bessant et al., Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP 12) and mutation analysis of the candidate gene RGS16 (RGS-r), J MED GENET, 37(5), 2000, pp. 384-387
Extragenic suppressors of the nimX2(cdc2) mutation of Aspergillus nidulansaffect nuclear division, septation and conidiation
Authors: McGuire, SL Roe, DL Carter, BW Carter, RL Grace, SP Hays, PL Lang, GA Mamaril, JLC McElvaine, A Payne, AM Schrader, MD Wahrle, SE Young, CD
Citation: Sl. Mcguire et al., Extragenic suppressors of the nimX2(cdc2) mutation of Aspergillus nidulansaffect nuclear division, septation and conidiation, GENETICS, 156(4), 2000, pp. 1573-1584
Familial cavernous hemangioma - An expanding ocular spectrum
Authors: Sarraf, D Payne, AM Kitchen, ND Sehmi, KS Downes, SM Bird, AC
Citation: D. Sarraf et al., Familial cavernous hemangioma - An expanding ocular spectrum, ARCH OPHTH, 118(7), 2000, pp. 969-973
The effect of chlorine on dopant activation in hydrogenated amorphous silicon
Authors: Payne, AM Wagner, S
Citation: Am. Payne et S. Wagner, The effect of chlorine on dopant activation in hydrogenated amorphous silicon, APPL PHYS L, 76(20), 2000, pp. 2949-2951
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
Authors: den Hollander, AI ten Brink, JB de Kok, YJM van Soest, S van den Born, LI van Driel, MA van de Pol, DJR Payne, AM Bhattacharya, SS Kellner, U Hoyng, CB Westerveld, A Brunner, HG Bleeker-Wagemakers, EM Deutman, AF Heckenlively, JR Cremers, FPM Bergen, AAB
Citation: Ai. Den Hollander et al., Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12), NAT GENET, 23(2), 1999, pp. 217-221
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa
Authors: Bessant, DAR Payne, AM Mitton, KP Wang, QL Swain, PK Plant, C Bird, AC Zack, DJ Swaroop, A Bhattacharya, SS
Citation: Dar. Bessant et al., A mutation in NRL is associated with autosomal dominant retinitis pigmentosa, NAT GENET, 21(4), 1999, pp. 355-356
Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies
Authors: Payne, AM Downes, SM Bessant, DAR Plant, C Moore, T Bird, AC Bhattacharya, SS
Citation: Am. Payne et al., Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies, J MED GENET, 36(9), 1999, pp. 691-693
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32
Authors: Bessant, DAR Anwar, K Khaliq, S Hameed, A Ismail, M Payne, AM Mehdi, SQ Bhattacharya, SS
Citation: Dar. Bessant et al., Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32, BR J OPHTH, 83(8), 1999, pp. 919-922
Clinical features of codon 172 RDS macular dystrophy - Similar phenotype in 12 families
Authors: Downes, SM Fitzke, FW Holder, GE Payne, AM Bessant, DAR Bhattacharya, SS Bird, AC
Citation: Sm. Downes et al., Clinical features of codon 172 RDS macular dystrophy - Similar phenotype in 12 families, ARCH OPHTH, 117(10), 1999, pp. 1373-1383
Refinement of the locus for autosomal recessive retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin
Authors: Khaliq, S Hameed, A Ismail, M Mehdi, SQ Bessant, DAR Payne, AM Bhattacharya, SS
Citation: S. Khaliq et al., Refinement of the locus for autosomal recessive retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin, AM J HU GEN, 65(2), 1999, pp. 571-574
Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patients
Authors: Kucinskas, V Payne, AM Ambrasiene, D Jurgelevicius, V Steponaviciute, D Arciuliene, JV Daktaraviciene, E Bhattacharya, S
Citation: V. Kucinskas et al., Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patients, HUMAN HERED, 49(2), 1999, pp. 71-74
Risultati: 1-23 |