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., Van De Pol, DJR., Payne, AM., Bhattacharya, SS., Kellner, U., Hoyng, CB., Westerveld, A., Brunner, HG., Bleeker-Wagemakers, EM., Deutman, AF., Heckenlively, JR., Cremers, FPM. and Bergen, AAB. 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 Bhattacharya, SS. 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., Payne, AM. and Bhattacharya, SS. 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 Bhattacharya, SS. 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

Gubb, D., Green, C., Huen, D., Coulson, D., Johnson, G., Tree, D., Collier, S. and Roote, J. 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 Kearney, L. 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., Bird, AC., Zack, DJ., Swaroop, A. and Bhattacharya, SS. 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., Bird, AC., Zack, DJ., Swaroop, A. and Bhattacharya, SS. 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., Cook, J., Xu, S., Bessant, DAR., Payne, AM., Chen, S., Zack, D., Sieving, PA. and Bhattacharya, SS. 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 Lansdorp, P. 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., Biondi, A. and Kearney, 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

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

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

Themis, M., Schneider, H., Kiserud, T., Cook, T., Adebakin, S., Jezzard, S., Forbes, S., Hanson, M., Pavirani, A., Rodeck, C. and Coutelle, C. 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

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

Schneider, H., Adebakin, S., Themis, M., Cook, T., Douar, AM., Pavirani, A. and Coutelle, C. 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

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

Grammatopoulos, DK., Dai, Y., Randeva, HS., Levine, MA., Karteris, E., Easton, AJ. and Hillhouse, EW. 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

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

Payne, AM., Khaliq, S., Hameed, A., Ismail, M., Bessant, DAR., Mehdi, SQ. and Bhattacharya, SS. et al. (1999) 'Localisation of a gene for autosomal recessive cone-rod dystrophy to chromosome'. Investigative Ophthalmology and Visual Science, 40 (4). pp. 16624 - 16624. ISSN: 1552-5783

Bessant, DAR., Anwar, K., Khaliq, S., Hameed, A., Ismail, M., Payne, AM., Mehdi, SQ. and Bhattacharya, SS. 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

Hameed, A., Khaliq, S., Ismail, M., Ebenezer, ND., Jordan, T., Mehdi, SQ., Payne, AM. and Bhattacharya, SS. et al. (1999) 'A novel locus for Leber congential amaurosis (LCA) with anterior keratoconus mapping to chromosome'. American Journal of Human Genetics, 65 (4). pp. 1408 - 1408. ISSN: 1537-6605

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

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]

Kučinskas, V., Payne, AM., Ambrasiene, D., Jurgelevičius, V., Steponavičiute, D., Arčiuliene, JV., Daktaravičiene, E. and Bhattacharya, S. 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 Bhattacharya, SS. 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

Swaroop, A., Evans, A., Swain, PK., Wang, QL., Mitton, K., Wu, W., Cook, J., Xu, S., Bessant, DAR., Payne, AM., Chen, S., Zack, D., Sieving, PA. and Bhattacharya, SS. 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

Downes, SM., Fitzke, FW., Holder, GE., Payne, AM., Bessant, DAR., Bhattacharya, SS. and Bird, AC. 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

Payne, AM., Downes, SM., Bessant, DAR., Plant, C., Moore, T., Bird, AC. and Bhattacharya, SS. 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

Khaliq, S., Hameed, A., Ismail, M., Mehdi, SQ., Bessant, DAR., Payne, AM. and Bhattacharya, SS. 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

Grammatopoulos, D., Dai, Y., Chen, J., Karteris, E., Papadopoulou, N., Easton, AJ. and Hillhouse, EW. et al. (1998) 'Human corticotropin-releasing hormone receptor: Differences in subtype expression between pregnant and nonpregnant myometria'. Journal of Clinical Endocrinology and Metabolism, 83 (7). pp. 2539 - 2544. ISSN: 0021-972X

Höfken, T., Linder, D., Kleene, R., Göke, B. and Wagner, ACC. (1998) 'Membrane dipeptidase and glutathione are major components of pig pancreatic zymogen granules'. Experimental Cell Research, 244 (2). pp. 481 - 490. ISSN: 0014-4827

Slijepcevic, P. (1998) 'Telomere length regulation - A view from the individual chromosome perspective'. Experimental Cell Research, 244 (1). pp. 268 - 274. ISSN: 0014-4827

Votruba, M., Payne, A., Moore, AT. and Bhattacharya, SS. (1998) 'Dominant optic atrophy: Exclusion and fine genetic mapping of the candidate gene, HRY'. Mammalian Genome, 9 (10). pp. 784 - 787. ISSN: 0938-8990

Kortenkamp, A. and Altenburger, R. (1998) 'Synergisms with mixtures of xenoestrogens: A reevaluation using the method of isoboles'. Science of the Total Environment, 221 (1). pp. 59 - 73. ISSN: 0048-9697

Themis, M., Forbes, SJ., Chan, L., Cooper, RG., Etheridge, CJ., Miller, AD., Hodgson, HJ. and Coutelle, C. et al. (1998) 'Enhanced in vitro and in vivo gene delivery using cationic agent complexed retrovirus vectors'. Gene Therapy, 5 (9). pp. 1180 - 1186. ISSN: 0969-7128

Slijepcevic, P. (1998) 'Telomere length and telomere-centromere relationships?'.4th International Symposium on Chromosomal Aberrations. UNIV ESSEN, ESSEN, GERMANY. 3 - 29 August. Elsevier BV. pp. 215 - 220. ISSN: 0027-5107

Roberts, T., Chernova, O. and Cowell, JK. (1998) 'NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma'. Human Molecular Genetics, 7 (7). pp. 1169 - 1178. ISSN: 0964-6906

Kelsell, RE., Gregory-Evans, K., Payne, AM., Perrault, I., Kaplan, J., Yang, RB., Garbers, DL., Bird, AC., Moore, AT. and Hunt, DM. et al. (1998) 'Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy'. Human Molecular Genetics, 7 (7). pp. 1179 - 1184. ISSN: 0964-6906

King, JA., Bridger, JM., Löchelt, M., Lichter, P., Schulz, TF., Schirrmacher, V. and Khazaie, K. et al. (1998) 'Nucleocytoplasmic transport of HTLV-1 RNA is regulated by two independent LTR encoded nuclear retention elements'. Oncogene, 16 (25). pp. 3309 - 3316. ISSN: 0950-9232

Kortenkamp, A. (1998) 'Chromium biomonitoring - Achievements, problems, and future challenges'.2nd International Symposium on Metals and Genetics. TORONTO, CANADA. 26 - 29 May. KLUWER ACADEMIC/PLENUM PUBL. pp. 87 - 100.

Slijepcevic, P. (1998) 'Telomeres and mechanisms of Robertsonian fusion'. Chromosoma, 107 (2). pp. 136 - 140. ISSN: 0009-5915