
CenGEM
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
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
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
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
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
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
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
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
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
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., 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., 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 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
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
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
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
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
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
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
Sohocki, MM., Perrault, I., Leroy, BP., Payne, AM., Dharmaraj, S., Bhattacharya, SS., et al. (2000) 'Prevalence of AIPL1 mutations in inherited retinal degenerative disease'. Molecular Genetics and Metabolism, 70 (2). pp. 142 - 150. ISSN: 1096-7192
Bessant, DAR., Payne, AM., Snow, BE., Antinolo, G., Mehdi, SQ., Bird, AC., 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
Lehmann, OJ., Ebenezer, ND., Jordan, T., Fox, M., Ocaka, L., Payne, A., 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
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
Cazzaniga, G., Tosi, S., Aloisi, A., Giudici, G., Daniotti, M., Pioltelli, P., 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 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., 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 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
Den Hollander, AI., Ten Brink, JB., De Kok, YJM., Van Soest, S., Van Den Born, LI., Van Driel, MA., et al. (1999) 'Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)'. Nature Genetics, 23 (2). pp. 217 - 221. ISSN: 1061-4036
Khaliq, S., Hameed, A., Ismail, M., Mehdi, SQ., Bessant, DAR., Payne, AM. and et al. (1999) 'Refinement of the locus for autosomal recessive retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.'. UNIV CHICAGO PRESS. pp. A257 - A257. ISSN: 0002-9297
Hameed, A., Khaliq, S., Ismail, M., Ebenezer, ND., Jordan, T., Mehdi, SQ., et al. (1999) 'A novel locus for Leber congential amaurosis (LCA) with anterior keratoconus mapping to chromosome 17p13.'. UNIV CHICAGO PRESS. pp. A253 - A253. ISSN: 0002-9297
Payne, AM., Khaliq, S., Hameed, A., Ismail, M., Bessant, DAR., Mehdi, SQ. and et al. (1999) 'Localisation of a gene for autosomal recessive cone-rod dystrophy to chromosome 17p12-13.3.'. UNIV CHICAGO PRESS. pp. A439 - A439. ISSN: 0002-9297
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
Forbes, SJ., Fajinmi, MA., Themis, M., Alison, MR., Coutelle, C. and Hodgson, HH. (1999) 'Gene transfer to the carbon tetrachloride damaged rat liver in vivo with adenoviral and retroviral based vectors'. 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
Gubb, D., Green, C., Huen, D., Coulson, D., Johnson, G., Tree, D., et al. (1999) 'The balance between isoforms of the Prickle LIM domain protein is critical for planar polarity in Drosophila imaginal discs'. Genes and Development, 13 (17). pp. 2315 - 2327. ISSN: 0890-9369
Kortenkamp, A. and Altenburger, R. (1999) 'Approaches to assessing combination effects of oestrogenic environmental pollutants'. Science of the Total Environment, 233 (1-3). pp. 131 - 140. ISSN: 0048-9697
Tosi, S., Scherer, SW., Giudici, G., Rambaldi, A., Czepulkowski, B., Biondi, A. and et al. (1999) 'Delineation of multiple deleted regions in 7q in myeloid disorders.'. Genes Chromosomes Cancer, 25 (4). pp. 384 - 392. ISSN: 1045-2257
Payne, AM., Bessant, DAR., Mitton, KP., Wang, QL., Swain, KP., Plant, C., et al. (1999) 'A mutation in the bZIP transcription factor NRL is associated with autosomal dominant retinitis pigmentosa in a family linked to a novel locus'. Nat Genet, 21 (4). pp. 355 - 356.
Bessant, DAR., Payne, AM., Mitton, KP., Wang, Q-L., Swain, PK., Plant, C., et al. (1999) 'A mutation in NRL is associated with autosomal dominant retinitis pigmentosa'. Nature Genetics, 21 (4). pp. 355 - 356. ISSN: 1061-4036
Swaroop, A., Evens, A., Swain, PK., Wang, QL., Mitton, K., Wu, W., et al. (1999) 'Gene regulation and retinal diseases: Studies on NRL, CRX and associated transcription factors'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S166 - S166. ISSN: 0146-0404
Payne, AM., Khaliq, S., Hameed, A., Bessant, DA., Mehdi, SQ. and Bhattacharya, SS. (1999) 'Localisation of a gene for autosomal recessive cone-rod dystrophy to chromosome 17p12-13.3'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S603 - S603. ISSN: 0146-0404