CenGEM
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
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
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
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
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
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
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
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
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'. 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 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
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
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
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
Hande, P., Slijepcevic, P., Silver, A., Bouffler, S., Van Buul, P., Bryant, P. and et al. (1999) 'Elongated telomeres in scid mice'. 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
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
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]
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
Kučinskas, V., Payne, AM., Ambrasiene, D., Jurgelevičius, V., Steponavičiute, D., Arčiuliene, JV., 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, DA., 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). Mutations in brief no. 208. Online.'. Human mutation, 13 (1). pp. 83. ISSN: 1059-7794
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
Downes, SM., Fitzke, FW., Holder, GE., Payne, AM., Bessant, DAR., Bhattacharya, SS. and et al. (1999) 'Clinical features of codon 172 RDS macular dystrophy: Similar phenotype in 12 families'. Archives of Ophthalmology, 117 (10). pp. 1373 - 1383. ISSN: 0003-9950
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) kinked to chromosome 6q in a family of pakistani origin [6]'. American Journal of Human Genetics, 65 (2). pp. 571 - 574. ISSN: 0002-9297
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
Wagner, ACC., Metzler, W., Höfken, T., Weber, H. and Göke, B. (1999) 'p38 Map kinase is expressed in pancreas and is immediately activated following Cerulein hyperstimulation'. Digestion, 60 (1). pp. 41 - 47. ISSN: 0012-2823
Slijepcevic, P. and Hande, MP. (1999) 'Chinese hamster telomeres are comparable in size to mouse telomeres'. Cytogenetics and Cell Genetics, 85 (3-4). pp. 196 - 199. ISSN: 0301-0171
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
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
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'. Journal of Gene Medicine, 1 (6). pp. 424 - 432. ISSN: 1099-498X
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
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
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