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Bessant, DAR., Payne, AM., Plant, C., Bird, AC., Swaroop, A. and Bhattacharya, SS. (2000) 'NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies'. European Journal of Human Genetics, 8 (10). pp. 783 - 787. ISSN: 1018-4813

Mellor, N., Themis, M., Selden, C., Jones, M. and Hodgson, HJ. (2000) 'Amelioration of murine histidinaemia using retroviral gene transfer'. Hepatology, 32 (4). pp. 182A - 182A. ISSN: 1527-3350

Fernando, S., Tosi, S., Conforti, L., Tarlton, A., Buckmaster, EA., Perry, VH., Smith, AD. and Coleman, MP. et al. (2000) 'Characterisation of the human homologus of a candidate gene for Slow Wallerian degeneration (Abstract)'. UNIV CHICAGO PRESS. pp. 178 - 178. ISSN: 0002-9297

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Höfken, T., Keller, N., Fleischer, F., Göke, B. and Wagner, ACC. (2000) 'Map kinase phosphatases (MKP's) are early responsive genes during induction of cerulein hyperstimulation pancreatitis'. Biochemical and Biophysical Research Communications, 276 (2). pp. 680 - 685. ISSN: 0006-291X

Gopalkrishnan, RV., Roberts, T., Tuli, S., Kang, DC., Christiansen, KA. and Fisher, PB. (2000) 'Molecular characterization of Prostate Carcinoma Tumor Antigen-1, PCTA-1, a human Galectin-8 related gene'. Oncogene, 19 (38). pp. 4405 - 4416. ISSN: 0950-9232

Stevenson, E., Sachdev, R., Anderson, R. and Maher, EJ. (2000) 'Identification of a marker chromosome by multiplex fluorescence in situ hybridisation (M-FISH)'. BRITISH MED JOURNAL PUBL GROUP. pp. S54 - S54. ISSN: 0022-2593

Schneider, H., Groves, M., Mühle, C., Reynolds, PN., Knight, A., Themis, M., Carvajal, J., Scaravilli, F., Curiel, DT., Fairweather, NF. and Coutelle, C. et al. (2000) 'Retargeting of adenoviral vectors to neurons using the Hc fragment of tetanus toxin'. Gene Therapy, 7 (18). pp. 1584 - 1592. ISSN: 0969-7128

Sarraf, D., Payne, AM., Kitchen, ND., Sehmi, KS., Downes, SM. and Bird, AC. (2000) 'Familial cavernous hemangioma: An expanding ocular spectrum'. Archives of Ophthalmology, 118 (7). pp. 969 - 973. ISSN: 1538-3601

PEREIRA, G. (2000) 'The Bub2p Spindle Checkpoint Links Nuclear Migration with Mitotic Exit'. Molecular Cell, 6 (1). pp. 1 - 10. ISSN: 1097-2765

Scheller, J., Schürer, A., Rudolph, C., Hettwer, S. and Kramer, W. (2000) 'MPH1, a yeast gene encoding a DEAH protein, plays a role in protection of the genome from spontaneous and chemically induced damage'. Genetics, 155 (3). pp. 1069 - 1081. ISSN: 0016-6731

Makarov, EM., Makarova, OV., Achsel, T. and Lührmann, R. (2000) 'The human homologue of the yeast splicing factor Prp6p contains multiple TPR elements and is stably associated with the U5 snRNP via protein-protein interactions.'. J Mol Biol, 298 (4). pp. 567 - 575. ISSN: 0022-2836

Slijepcevic, P., Xiao, Y. and Natarajan, AT. (2000) 'Chromosome-specific telomeric associations in Chinese hamster embryonic cells'. Genes Chromosomes Cancer, 28 (1). pp. 98 - 105. ISSN: 1045-2257

Forbes, SJ., Themis, M., Alison, MR., Shiota, A., Kobayashi, T., Coutelle, C. and Hodgson, HJ. et al. (2000) 'Tri-iodothyronine and a deleted form of hepatocyte growth factor act synergistically to enhance liver proliferation and enable in vivo retroviral gene transfer via the peripheral venous system'. Gene Therapy, 7 (9). pp. 784 - 789. ISSN: 0969-7128

McKay, TR., MacVinish, LJ., Carpenter, B., Themis, M., Jezzard, S., Goldin, R., Pavirani, A., Hickman, ME., Cuthbert, AW. and Coutelle, C. et al. (2000) 'Selective in vivo transfection of murine biliary epithelia using polycation-enhanced adenovirus'. Gene Therapy, 7 (8). pp. 644 - 652. ISSN: 0969-7128

Hofken, T., Keller, N., Burkhard, G. and Wagner, AC. (2000) 'Map kinase phosphatases (MKPS) are early responsive genes during induction of cerulein hyperstimulation pancreatitis'. Elsevier BV. pp. A171 - A171. ISSN: 0016-5085

Payne, J., Jones, C., Lakhani, S. and Kortenkamp, A. (2000) 'Improving the reproducibility of the MCF-7 cell proliferation assay for the detection of xenoestrogens'. Science of the Total Environment, 248 (1). pp. 51 - 62. ISSN: 0048-9697

Venables, JP. (2000) 'RBMY, a probable human spermatogenesis factor, and other hnRNP G proteins interact with Tra2beta and affect splicing'. Human Molecular Genetics, 9 (5). pp. 685 - 694. ISSN: 0964-6906

Bessant, DAR., Payne, AM., Holder, G., Fitzke, F., Bhattachayra, SS. and Bird, AC. (2000) 'Phenotype of autosomal dominant retinitis pigmentosa associated with the S50T mutation in the NRL gene.'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S193 - S193. ISSN: 0146-0404

Downes, SM., Payne, AM., Kapsali, J., Holder, GE., Fitzke, FW., Bhattacharya, SS. and Bird, AC. et al. (2000) 'Mutational analysis and phenotype characterisation in Best vitelliform dystrophy.'. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 41 (4). pp. S886 - S886. ISSN: 0146-0404

Sohocki, MM., Perrault, I., Payne, AM., Kaplan, J., Bhattacharya, SS., Birch, DG., Heckenlively, JR. and Daiger, SP. et al. (2000) 'Mutations in AIPL1, a novel photoreceptor/pineal-expressed gene on 17P13, cause leber congenital amaurosis (LCA34).'. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 41 (4). pp. S94 - S94. ISSN: 0146-0404

Payne, AM., Khaliq, S., Hameed, A., Ismail, M., Anwar, K., Bessant, D., Mehdi, SQ. and Bhattacharya, SS. et al. (2000) 'A new locus for autosomal recessive retinitis pigmentosa mapping to chromosome 4q32-34.'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S194 - S194. ISSN: 0146-0404

Kaushal, S., Vithana, EN., Abu-Safieh, L., Payne, AM. and Bhattacharya, SS. (2000) 'Mutation screening of RPE G-coupled protein receptor (RGR) in retinitis pigmentosa.'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S194 - S194. ISSN: 0146-0404

Bhattacharya, SS., Khaliq, S., Hameed, A., Ismail, M., Anwar, K., Leroy, B., Mehdi, SQ. and Payne, AM. et al. (2000) 'A new locus for autosomal recessive cone-rod dystrophy mapping to chromosome 1q12-24.'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S195 - S195. ISSN: 0146-0404

Aragon-Martin, JA., Leroy, BP., Prescott, QC., Sohocki, MM., Daiger, SP., Bird, AC., Meire, FM., Payne, AM. and Bhattacharya, SS. et al. (2000) 'Analysis of the AIPLI gene in Belgian and British patients with leber congenital amaurosis.'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S196 - S196. ISSN: 0146-0404

Leroy, BP., Aragon-Martin, JA., Weston, MD., Bessant, DAR., Bird, AC., Kimberling, WJ., Payne, AM. and Bhattacharya, SS. et al. (2000) 'Mutations in laminush British Usher type II patients.'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S195 - S195. ISSN: 0146-0404

Forbes, SJ., Themis, M., Alison, MR., Sarosi, I., Coutelle, C. and Hodgson, HJ. (2000) 'Synergistic growth factors enhance rat liver proliferation and enable retroviral gene transfer via a peripheral vein'. Gastroenterology, 118 (3). pp. 591 - 598. ISSN: 0016-5085

Jones, C., Payne, J., Wells, D., Delhanty, JDA., Lakhani, SR. and Kortenkamp, A. (2000) 'Comparative genomic hybridization reveals extensive variation among different MCF-7 cell stocks'. Cancer Genetics and Cytogenetics, 117 (2). pp. 153 - 158. ISSN: 0165-4608

Hameed, A., Shagufta, K., Ismail, M., Anwar, K., Ebenezer, N., Jordan, T., Mehdi, K., Payne, AM. and Bhattacharya, S. et al. (2000) 'A novel locus for leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13'. Investigative Ophthalmology and Visual Science, 41 (3). pp. 629 - 633. ISSN: 1552-5783

Jones, C. and Kortenkamp, A. (2000) 'RAPD library fingerprinting of bacterial and human DNA: Applications in mutation detection'. Teratogenesis Carcinogenesis and Mutagenesis, 20 (2). pp. 49 - 63. ISSN: 0270-3211

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. and Daiger, SP. et al. (2000) 'Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis'. Nature Genetics, 24 (1). pp. 79 - 83. ISSN: 1061-4036

Papaioannou, M., Ocaka, L., Bessant, D., Lois, N., Bird, A., Payne, A. and Bhattacharya, S. et al. (2000) 'An analysis of ABCR mutations in British patients with recessive retinal dystrophies'. Investigative Ophthalmology and Visual Science, 41 (1). pp. 16 - 19. ISSN: 0146-0404

Pereira, G., Höfken, T., Grindlay, J., Manson, C. and Schiebel, E. (2000) 'The Bub2p spindle checkpoint links nuclear migration with mitotic exit'. Molecular Cell, 6 (1). pp. 1 - 10. ISSN: 1097-2765

Payne, J., Rajapakse, N., Wilkins, M. and Kortenkamp, A. (2000) 'Prediction and assessment of the effects of mixtures of four xenoestrogens'. Environmental Health Perspectives, 108 (10). pp. 983 - 987. ISSN: 0091-6765 Open Access Link

Lehmann, OJ., Ebenezer, ND., Jordan, T., Fox, M., Ocaka, L., Payne, A., Leroy, BP., Clark, BJ., Hitchings, RA., Povey, S., Khaw, PT. and Bhattacharya, SS. et al. (2000) 'Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma'. American Journal of Human Genetics, 67 (5). pp. 1129 - 1135. ISSN: 0002-9297

Bessant, DAR., Payne, AM., Snow, BE., Antinolo, G., Mehdi, SQ., Bird, AC., Siderovski, DP. and Bhattacharya, SS. et al. (2000) 'Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)'. Journal of Medical Genetics, 37 (5). pp. 384 - 387. ISSN: 0022-2593

Sohocki, MM., Perrault, I., Leroy, BP., Payne, AM., Dharmaraj, S., Bhattacharya, SS., Kaplan, J., Maumenee, IH., Koenekoop, R., Meire, FM., Birch, DG., Heckenlively, JR. and Daiger, SP. et al. (2000) 'Prevalence of AIPL1 mutations in inherited retinal degenerative disease'. Molecular Genetics and Metabolism, 70 (2). pp. 142 - 150. ISSN: 1096-7192

Chelsea, DM., Roberts, T. and Cowell, JK. (2000) 'A new region of synteny between human chromosome 1p22 and mouse chromosome 5.'. International Journal of Molecular Medicine, 5 (5). pp. 553 - 556. ISSN: 1107-3756

Karteris, E., Grammatopoulos, D., Randeva, H. and Hillhouse, EW. (2000) 'Signal transduction characteristics of the corticotropin-releasing hormone receptors in the feto-placental unit'. Journal of Clinical Endocrinology and Metabolism, 85 (5). pp. 1989 - 1996. ISSN: 0021-972X

Anderson, RM., Marsden, SJ., Wright, EG., Kadhim, MA., Goodhead, DT. and Griffin, CS. (2000) 'Complex chromosome aberrations in peripheral blood lymphocytes as a potential biomarker of exposure to high-LET alpha-particles'. International Journal of Radiation Biology, 76 (1). pp. 31 - 42. ISSN: 0955-3002

Bridger, JM., Boyle, S., Kill, IR. and Bickmore, WA. (2000) 'Re-modelling of nuclear architecture in quiescent and senescent human fibroblasts'. Current Biology, 10 (3). pp. 149 - 152. ISSN: 0960-9822

Samper, E., Goytisolo, FA., Slijepcevic, P., Van Buul, PPW. and Blasco, MA. (2000) 'Mammalian Ku86 protein prevents telomeric fusions independently of the length of TTAGGG repeats and the G-strand overhang'. EMBO Reports, 1 (3). pp. 244 - 252. ISSN: 1469-221X

Cazzaniga, G., Tosi, S., Aloisi, A., Giudici, G., Daniotti, M., Pioltelli, P., Kearney, L. and Biondi, A. et al. (1999) 'The tyrosine kinase Abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): Molecular cloning of both reciprocal transcripts'. BLOOD, 94 (12). pp. 4370 - 4373. ISSN: 0006-4971

Cazzaniga, G., Tosi, S., Aloisi, A., Giudici, G., Pioltelli, P., Kearney, L. and Biondi, A. et al. (1999) 'The tyrosine kinase ABL-related gene "ARG" is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): Molecular cloning of both reciprocal transcripts. (Abstract)'. AMER SOC HEMATOLOGY. pp. 55A - 55A. ISSN: 0006-4971

Rajapakse, N. and Kortenkamp, A. (1999) 'Formation of DNA damage by 17 β-oestradiol in MCI-7 breast cancer cells'. Journal of Pharmacy and Pharmacology, 51 (SUPPL.). pp. 151. ISSN: 0022-3573

Kučinskas, V., Payne, AM., Ambrasiene, D., Jurgelevičius, V., Steponavičiute, D., Arčiuliene, JV., Daktaravičiene, E. and Bhattacharya, S. et al. (1999) 'Mutations in the human rhodopsin gene and polymorphisms in peripherin/RDS gene in Lithuanian autosomal dominant retinitis pigmentosa patients'. Journal of Applied Genetics, 40 (1). pp. 53 - 61. ISSN: 1234-1983

Casadevall, M., Da Cruz Fresco, P. and Kortenkamp, A. (1999) 'Chromium(VI)-mediated DNA damage: Oxidative pathways resulting in the formation of DNA breaks and abasic sites'. Chemico Biological Interactions, 123 (2). pp. 117 - 132. ISSN: 0009-2797

Cazzaniga, G., Tosi, S., Aloisi, A., Giudici, G., Pioltelli, P., Kearney, L. and Biondi, A. et al. (1999) 'The tyrosine kinase ABL-related gene "ARG" is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): Molecular cloning of both reciprocal transcripts. (Abstract)'.American Society of Hematology 41st annual meeting.. New Orleans, Louisiana, USA. 15 - 7 December. Amer soc hematology. pp. 55A - 55A. ISSN: 0006-4971

Mellor, N., Themis, M., Selden, C. and Hodgson, HJ. (1999) 'An in-vitro model of histidinemia ameliorated by a histidase encoding retrovirus'. Hepatology, 30 (4). pp. 514A - 514A. ISSN: 1527-3350

Klinger, HC., Bretland, AJ., Reid, SV., Chapple, CR. and Eaton, CL. (1999) 'Regulation of prostatic stromal cell growth and function by transforming growth factor beta (TGFβ)'. The Prostate, 41 (2). pp. 110 - 120. ISSN: 1097-0045