CenGEM
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
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
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
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
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., 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
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
Grammatopoulos, DK., Dai, Y., Randeva, HS., Levine, MA., Karteris, E., Easton, AJ. and et al. (1999) 'A Novel Spliced Variant of the Type 1 Corticotropin-Releasing Hormone Receptor with a Deletion in the Seventh Transmembrane Domain Present in the Human Pregnant Term Myometrium and Fetal Membranes'. Molecular Endocrinology, 13 (12). pp. 2189 - 2202. ISSN: 0888-8809
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
Schneider, H., Adebakin, S., Themis, M., Cook, T., Douar, AM., Pavirani, A. and et al. (1999) 'Therapeutic plasma concentrations of human factor IX in mice after gene delivery into the amniotic cavity: a model for the prenatal treatment of haemophilia B'. The Journal of Gene Medicine, 1 (6). pp. 424 - 432. ISSN: 1099-498X
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
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
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
Downes, SM. (1999) 'Clinical Features of Codon 172 RDSMacular Dystrophy'. Archives of Ophthalmology, 117 (10). pp. 1373 - 1373. ISSN: 0003-9950
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
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
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
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
Payne, AM., Downes, SM., Bessant, DAR., Plant, C., Moore, T., Bird, AC. and et al. (1999) 'Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies: Table 1'. Journal of Medical Genetics, 36 (9). pp. 691 - 693. ISSN: 0022-2593
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 & Development, 13 (17). pp. 2315 - 2327. ISSN: 0890-9369
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
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
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'. The American Journal of Human Genetics, 65 (2). pp. 571 - 574. ISSN: 0002-9297
Bessant, DAR., Anwar, K., Khaliq, S., Hameed, A., Ismail, M., Payne, AM., et al. (1999) 'Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32'. British Journal of Ophthalmology, 83 (8). pp. 919 - 922. ISSN: 0007-1161
Metzler, W., Höfken, T., Weber, H., Printz, H., Göke, B. and Wagner, ACC. (1999) 'Hyperthermia, Inducing Pancreatic Heat-Shock Proteins, Fails to Prevent Cerulein-Induced Stress Kinase Activation'. Pancreas, 19 (2). pp. 150 - 157. ISSN: 0885-3177
Themis, M., Schneider, H., Kiserud, T., Cook, T., Adebakin, S., Jezzard, S., et al. (1999) 'Successful expression of β-galactosidase and factor IX transgenes in fetal and neonatal sheep after ultrasound-guided percutaneous adenovirus vector administration into the umbilical vein'. Gene Therapy, 6 (7). pp. 1239 - 1248. ISSN: 0969-7128
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
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.
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
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
Bhattacharya, SS., Bessant, DA., Payne, AM., Mitton, KP., Zack, DJ. and Swaroop, A. (1999) 'A mutation in the BZIP transcription factor NRL is associated with autosomal dominant retinitis pigmentosa in a family linked to a novel locus at 14q11'. ASSOC RESEARCH VISION OPHTHALMOLOGY INC. pp. S564 - S564. ISSN: 0146-0404
Hande, P., Slijepcevic, P., Silver, A., Bouffler, S., van Buul, P., Bryant, P. and et al. (1999) 'Elongated Telomeres inscidMice'. Genomics, 56 (2). pp. 221 - 223. ISSN: 0888-7543
Tosi, S., Giudici, G., Rambaldi, A., Scherer, SW., Bray-Ward, P., Dirscherl, L., et al. (1999) 'Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization'. Genes, Chromosomes and Cancer, 24 (3). pp. 213 - 221. ISSN: 1045-2257
Craig, JM., Earnshaw, WC. and Vagnarelli, P. (1999) 'Mammalian Centromeres: DNA Sequence, Protein Composition, and Role in Cell Cycle Progression'. Experimental Cell Research, 246 (2). pp. 249 - 262. ISSN: 0014-4827
Wagner, ACC., Metzler, W., Höfken, T., Weber, H. and Göke, B. (1999) 'p38 Map Kinase Is Expressed in the Pancreas and Is Immediately Activated following Cerulein Hyperstimulation'. Digestion, 60 (1). pp. 41 - 47. ISSN: 0012-2823
Kučinskas, V., Payne, A., Ambrasienė, D., Jurgelevičius, V., Steponavičiūtė, D., Arčiulienė, J., et al. (1999) 'Molecular Genetic Study of Autosomal Dominant Retinitis pigmentosa in Lithuanian Patients'. Human Heredity, 49 (2). pp. 71 - 74. ISSN: 0001-5652
Bessant, DAR., Khaliq, S., Hameed, A., Anwar, K., Payne, AM., Mehdi, SQ. and et al. (1999) 'Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu)'. Human Mutation, 13 (1). pp. 83 - 83. ISSN: 1059-7794
Su, G., Roberts, T. and Cowell, JK. (1999) 'TTC4,a Novel Human Gene Containing the Tetratricopeptide Repeat and Mapping to the Region of Chromosome 1p31 That Is Frequently Deleted in Sporadic Breast Cancer'. Genomics, 55 (2). pp. 157 - 163. ISSN: 0888-7543
Bickmore, WA. and Bridger, JM. (1999) 'Meeting Report of HUGO Spatial Organisation of the Genome workshop, Edinburgh, UK, 14-15 May 1999: A sense of time and place'. Chromosome Research, 7 (6). pp. 425 - 429. ISSN: 0967-3849
Bhattacharya, SS., Bessant, DAR., Payne, AM., Mitton, KP., Zack, DJ. and Swaroop, A. (1999) 'A mutation in the bZIP transcription factor NRL is associated with autosomal dominant retinitis pigmentosa in a family linked to a novel locus at 14q11'.ARVO 1999. [unpublished]
Tosi, S., Cazzaniga, G., Giudici, G., Marynen, P., Kearney, L. and Blondi, A. (1999) 'Heterogeneity of breakpoints on 12p in patients with myeloid disorders. (Abstract)'. Karger. pp. 88 - 88. ISSN: 0301-0171
Tosi, S., Cazzaniga, G., Giudici, G., Marynen, P., Kearney, L. and Biondi, A. (1999) 'Heterogeneity of breakpoints on 12p in patients with myeloid disorders (Absract)'. CYTOGENET CELL GENET, 85 (1-2). pp. 88 - 88. ISSN: 0301-0171
Slijepcevic, P. and Hande, MP. (1999) 'Chinese hamster telomeres are comparable in size to mouse telomeres'. Cytogenetic and Genome Research, 85 (3-4). pp. 196 - 199. ISSN: 1424-8581
Bickmore, WA. and Bridger, JM. (1999) 'A sense of time and place: Meeting report of HUGO spatial organisation of the genome workshop, Edinburgh, 14-15 May 1999'. Chromosome Research, 7 (6). pp. 425 - 429. ISSN: 0967-3849
Croft, JA., Bridger, JM., Boyle, S., Perry, P., Teague, P. and Bickmore, WA. (1999) 'Differences in the localization and morphology of chromosomes in the human nucleus'. Journal of Cell Biology, 145 (6). pp. 1119 - 1131. ISSN: 0021-9525 Open Access Link
Swaroop, A., Evans, 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'. Investigative Ophthalmology and Visual Science, 40 (4). pp. 891 - 891. ISSN: 1552-5783