CenGEM
Payne, AM., Morris, AG., Downes, SM., Johnsson, S., Bird, AC., Moore, AT., et al. (2001) 'Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies'. Journal of Medical Genetics, 38 (9). pp. 611 - 614. ISSN: 0022-2593
Weston, BS., Wahab, NA., Roberts, T. and Mason, RM. (2001) 'Bacitracin inhibits fibronectin matrix assembly by mesangial cells in high glucose'. Kidney International, 60 (5). pp. 1756 - 1764. ISSN: 0085-2538
Carvalho, C., Pereira, HM., Ferreira, J., Pina, C., Mendonça, D., Rosa, AC. and et al. (2001) 'Chromosomal G-dark bands determine the spatial organization of centromeric heterochromatin in the nucleus'. Molecular Biology of the Cell, 12 (11). pp. 3563 - 3572. ISSN: 1059-1524
David, AL., Themis, M., Cook, T., Coutelle, C. and Rodeck, CH. (2001) 'Fetal gene therapy'. Ultrasound Review of Obstetrics and Gynecology, 1 (1). pp. 14 - 27. ISSN: 1472-2240
Downes, SM., Payne, AM., Kelsell, RE., Fitzke, FW., Holder, GE., Hunt, DM., et al. (2001) 'Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1'. Archives of Ophthalmology, 119 (11). pp. 1667 - 1673. ISSN: 0003-9950
Adams, RR., Eckley, DM., Vagnarelli, P., Wheatley, SP., Gerloff, DL., Mackay, AM., et al. (2001) 'Human INCENP colocalizes with the Aurora-B/AIRK2 kinase on chromosomes and is overexpressed in tumour cells'. Chromosoma, 110 (2). pp. 65 - 74. ISSN: 0009-5915
Putzrath, RM. and Kortenkamp, A. (2001) 'Inaccurate models for mixtures (multiple letters) [4]'. Environmental Health Perspectives, 109 (2). pp. A64 - A65. ISSN: 0091-6765
Payne, J., Scholze, M. and Kortenkamp, A. (2001) 'Mixtures of four organochlorines enhance human breast cancer cell proliferation'. Environmental Health Perspectives, 109 (4). pp. 391 - 397. ISSN: 0091-6765 Open Access Link
Karteris, E., Randeva, HS., Grammatopoulos, DK., Jaffe, RB. and Hillhouse, EW. (2001) 'Expression and coupling characteristics of the CRH and orexin type 2 receptors in human fetal adrenals'. Journal of Clinical Endocrinology and Metabolism, 86 (9). pp. 4512 - 4519. ISSN: 0021-972X
Karteris, E., Grammatopoulos, DK., Randeva, HS. and Hillhouse, EW. (2001) 'The role of corticotropin-releasing hormone receptors in placenta and fetal membranes during human pregnancy'. Molecular Genetics and Metabolism, 72 (4). pp. 287 - 296. ISSN: 1096-7192
Boyle, S., Gilchrist, S., Bridger, JM., Mahy, NL., Ellis, JA. and Bickmore, WA. (2001) 'The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells'. Human Molecular Genetics, 10 (3). pp. 211 - 219. ISSN: 0964-6906 Open Access Link
Randeva, HS., Karteris, E., Grammatopoulos, D. and Hillhouse, EW. (2001) 'Expression of orexin-a and functional orexin type 2 receptors in the human adult adrenals: Implications for adrenal function and energy homeostasis'. Journal of Clinical Endocrinology and Metabolism, 86 (10). pp. 4808 - 4813. ISSN: 0021-972X
Payne, A., Vithana, E., Khaliq, S., Hameed, A., Deller, J., Abu-Safieh, L., et al. (2000) 'RP1 protein truncating mutations predominate at the RP1 adRP locus'. Investigative Ophthalmology and Visual Science, 41 (13). pp. 4069 - 4073. ISSN: 0146-0404
Weber, H., Wagner, ACC., Jonas, L., Merkord, J., Hõfken, T., Nizze, H., et al. (2000) 'Heat shock response is associated with protection against acute interstitial pancreatitis in rats'. Digestive Diseases and Sciences, 45 (11). pp. 2252 - 2264. ISSN: 0163-2116
Tosi, S., Harbott, J., Haas, OA. and Harrison, C. (2000) 'A new non-random translocation involving ETV6 and a 7q36 partner associated with infant leukaemia'. Blood, 96 (11 PART II). ISSN: 0006-4971
Payne, AM., Vithana, E., Khaliq, S., Hameed, A., Kermani, S., Leroy, B., et al. (2000) 'Predominance of RP1 protein truncation underlies the pathogenicity of RP1 gene associated British and Pakistani adRP Patients'. Investigative Ophthalmology and Visual Science, 41 (13). pp. 4069 - 4073. ISSN: 1552-5783
Tosi, S., Harbott, J., Teigler-Schlegel, A., Haas, OA., Pirc-Danoewinata, H., Harrison, CJ., et al. (2000) 't(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia'. Genes Chromosomes and Cancer, 29 (4). pp. 325 - 332. ISSN: 1045-2257
Tosi, S., Harbott, J., Haas, OA., Harrison, C., Kempski, H., Cazzaniga, G., et al. (2000) 'A new non-random translocation involving ETV6 and a 7q36 partner associated with infant leukaemia. (Abstract)'. AMER SOC HEMATOLOGY. pp. 163B - 163B. ISSN: 0006-4971
Cazzaniga, G., Daniotti, M., Tosi, S., Giudici, G., Aloisi, A., Kearney, L. and et al. (2000) 'First evidence of a chimeric transcript involving the PAX5 gene in an all case carrying a t(9;12)(p13;p13) translocation. (Abstract)'.American Society of Hematology 47th Annual Meeting. Atlanta, Georgia. 16 - 13 December. AMER SOC HEMATOLOGY. pp. 690A - 691A. ISSN: 0006-4971
Khaliq, S., Hameed, A., Ismail, M., Anwar, K., Leroy, BP., Mehdi, SQ., et al. (2000) 'Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24'. Investigative Ophthalmology and Visual Science, 41 (12). pp. 3709 - 3712. ISSN: 0146-0404
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., 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
Fernando, S., Tosi, S., Conforti, L., Tarlton, A., Buckmaster, EA., Perry, VH., et al. (2000) 'Characterisation of the human homologue of a candidate gene for Slow Wallerian degeneration. (Abstract)'. UNIV CHICAGO PRESS. pp. 178. ISSN: 0002-9297
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., 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
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
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
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 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., 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
Downes, SM., Payne, AM., Kapsali, J., Holder, GE., Fitzke, FW., Bhattacharya, SS. and 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., 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., 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., 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
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
Aragon-Martin, JA., Leroy, BP., Prescott, QC., Sohocki, MM., Daiger, SP., Bird, AC., 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., et al. (2000) 'Mutations in laminush British Usher type II patients.'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S195 - S195. ISSN: 0146-0404
Hameed, A., Shagufta, K., Ismail, M., Anwar, K., Ebenezer, N., Jordan, T., 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
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
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., 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