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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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Conference paper

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

Journal article

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

Journal article

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

Journal article

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

Conference paper

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Conference paper

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

Conference paper

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

Conference paper

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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.

Journal article

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

Conference paper

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

Conference paper

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

Conference paper

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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]

Conference paper

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Conference paper

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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