Results: 1-25 | 26-50 | 51-51
Results: 1-25/51

Authors: Bhattacharya, SS Betz, U Hahn, H
Citation: Ss. Bhattacharya et al., Some studies on the superplastic deformation behavior of nanocrystalline yttria stabilised zirconia based ceramics, SCR MATER, 44(8-9), 2001, pp. 1553-1556

Authors: Vithana, EN Abu-Safieh, L Allen, MJ Carey, A Papaioannou, M Chakarova, C Al-Maghtheh, M Ebenezer, ND Willis, C Moore, AT Bird, AC Hunt, DM Bhattacharya, SS
Citation: En. Vithana et al., A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11), MOL CELL, 8(2), 2001, pp. 375-381

Authors: McKie, AB McHale, JC Keen, TJ Tarttelin, EE Goliath, R van Lith-Verhoeven, JJC Greenberg, J Ramesar, RS Hoyng, CB Cremers, FPM Mackey, DA Bhattacharya, SS Bird, AC Markham, AF Inglehearn, CF
Citation: Ab. Mckie et al., Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominantretinitis pigmentosa (RP13), HUM MOL GEN, 10(15), 2001, pp. 1555-1562

Authors: Newbold, RJ Deery, EC Walker, CE Wilkie, SE Srinivasan, N Hunt, DM Bhattacharya, SS Warren, MJ
Citation: Rj. Newbold et al., The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy, HUM MOL GEN, 10(1), 2001, pp. 47-54

Authors: Bessant, DAR Ali, RR Bhattacharya, SS
Citation: Dar. Bessant et al., Molecular genetics and prospects for therapy of the inherited retinal dystrophies, CUR OP GEN, 11(3), 2001, pp. 307-316

Authors: Thiselton, DL Alexander, C Morris, A Brooks, S Rosenberg, T Eiberg, H Kjer, B Kjer, P Bhattacharya, SS Votruba, M
Citation: Dl. Thiselton et al., A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect, HUM GENET, 109(5), 2001, pp. 498-502

Authors: Murray, S Halford, S Ebenezer, ND Gregory-Evans, CY Bhattacharya, SS
Citation: S. Murray et al., Assignment of BCL2L11 to human chromosome band 2p13 with somatic cell and radiation hybrids, CYTOG C GEN, 92(3-4), 2001, pp. 353-353

Authors: Rao, PMR Das, NC Sekhar, BNR Padmanabhan, S Shastri, A Bhattacharya, SS Roy, AP
Citation: Pmr. Rao et al., Photophysics beamline at Indus-1, NUCL INST A, 467, 2001, pp. 613-616

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

Authors: Sowden, JC Holt, JKL Meins, A Smith, HK Bhattacharya, SS
Citation: Jc. Sowden et al., Expression of Drosophila omb-related T-box genes in the developing human and mouse neural retina, INV OPHTH V, 42(13), 2001, pp. 3095-3102

Authors: Lehmann, OJ El-Ashry, MF Ebenezer, ND Ocaka, L Francis, PJ Wilkie, SE Patel, RJ Ficker, L Jordan, T Khaw, PT Bhattacharya, SS
Citation: Oj. Lehmann et al., A novel keratocan mutation causing autosomal recessive cornea plana, INV OPHTH V, 42(13), 2001, pp. 3118-3122

Authors: Khaliq, S Hameed, A Ismail, M Anwar, K Leroy, B Payne, AA Bhattacharya, SS Mehdi, SQ
Citation: S. Khaliq et al., Locus for autosomal recessive nonsyndromic persistent hyperplastic primaryvitreous, INV OPHTH V, 42(10), 2001, pp. 2225-2228

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

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

Authors: Reichel, MB Bainbridge, J Baker, D Thrasher, AJ Bhattacharya, SS Ali, RR
Citation: Mb. Reichel et al., An immune response after intraocular administration of an adenoviral vector containing a beta galactosidase reporter gene slows retinal degeneration in the rd mouse, BR J OPHTH, 85(3), 2001, pp. 341-344

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

Authors: Berry, V Francis, P Reddy, MA Collyer, D Vithana, E MacKay, I Dawson, G Carey, AH Moore, A Bhattacharya, SS Quinlan, RA
Citation: V. Berry et al., Alpha-b crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans, AM J HU GEN, 69(5), 2001, pp. 1141-1145

Authors: Wilkie, SE Li, Y Deery, EC Newbold, RJ Garibaldi, D Bateman, JB Zhang, H Lin, W Zack, DJ Bhattacharya, SS Warren, MJ Hunt, DM Zhang, K
Citation: Se. Wilkie et al., Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy, AM J HU GEN, 69(3), 2001, pp. 471-480

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

Authors: Alexander, C Votruba, M Pesch, UEA Thiselton, DL Mayer, S Moore, A Rodriguez, M Kellner, U Leo-Kottler, B Auburger, G Bhattacharya, SS Wissinger, B
Citation: C. Alexander et al., OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28, NAT GENET, 26(2), 2000, pp. 211-215

Authors: Ali, RR Sarra, GM Stephens, C de Alwis, M Bainbridge, JWB Munro, PM Fauser, S Reichell, MB Kinnon, C Hunt, DM Bhattacharya, SS Thrasher, AJ
Citation: Rr. Ali et al., Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy, NAT GENET, 25(3), 2000, pp. 306-310

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

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

Authors: Bhattacharya, SS Das, U
Citation: Ss. Bhattacharya et U. Das, Occurrence of Salmonella typhi infection in Rourkela, Orissa, I J MED RES, 111, 2000, pp. 75-76

Authors: Wilkie, SE Newbold, RJ Deery, E Walker, CE Stinton, I Ramamurthy, V Hurley, JB Bhattacharya, SS Warren, MJ Hunt, DM
Citation: Se. Wilkie et al., Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy, HUM MOL GEN, 9(20), 2000, pp. 3065-3073
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