
CenGEM
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
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
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
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
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
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
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
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
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
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
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]
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'. Investigative Ophthalmology and Visual Science, 40 (4). pp. 16624 - 16624. ISSN: 1552-5783
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'. American Journal of Human Genetics, 65 (4). pp. 1408 - 1408. ISSN: 1537-6605
Grammatopoulos, D., Dai, Y., Chen, J., Karteris, E., Papadopoulou, N., Easton, AJ. and 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., 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., 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 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
Elliott, DJ., Oghene, K., Makarov, G., Makarova, O., Hargreave, TB., Chandley, AC., et al. (1998) 'Dynamic changes in the subnuclear organisation of pre-mRNA splicing proteins and RBM during human germ cell development'. Journal of Cell Science, 111 (9). pp. 1255 - 1265. ISSN: 0021-9533
Slijepcevic, P. and Bryant, PE. (1998) 'Chromosome healing, telomere capture and mechanisms of radiation- induced chromosome breakage'. International Journal of Radiation Biology, 73 (1). pp. 1 - 13. ISSN: 0955-3002
Karteris, E., Grammatopoulos, D., Dai, Y., Olah, KB., Ghobara, TB., Easton, A. and et al. (1998) 'The human placenta and fetal membranes express the corticotropin-releasing hormone receptor 1alpha (CRH-1alpha) and the CRH-C variant receptor.'. J Clin Endocrinol Metab, 83 (4). pp. 1376 - 1379. ISSN: 0021-972X
Wilmen, A., Strowski, M., Höfken, T., Prinz, H., Göke, B. and Wagner, ACC. (1998) 'Differential regulation of pancreatic genes during experimental pancreatitis, investigated by differential display analysis'. Elsevier BV. pp. A510 - A510. ISSN: 0016-5085
Höfken, T., Linder, D., Kleene, R., Göke, B. and Wagner, ACC. (1998) 'Regulation of pancreatic membrane dipeptidase mRNA expression and identification as zymogen granule membrane protein by peptide sequencing'. Elsevier BV. pp. A469 - A469. ISSN: 0016-5085
Papaioannou, M., Payne, AM., Rougas, C., Bessant, D., Loutradis-Anagnostou, A., Balassopoulou, A. and et al. (1998) 'Mutation screening in the photoreceptor-specific gene (CRX) in patients of Greek origin'. Investigative Ophthalmology and Visual Science, 39 (4). ISSN: 1552-5783
Woodcock, SC., Raux, EC., Evans, A., Dalvin, ST., Payne, AM., Downes, SM., et al. (1998) 'Characterization of the Y99C mutant of a guanylate cyclase activator protein 1 (GCAP1)'. Investigative Ophthalmology and Visual Science, 39 (4). ISSN: 1552-5783
Slijepcevic, P. and Bryant, PE. (1998) 'Reply to J. P. Murnane's Letter to the Editor'. Radiation Research, 149 (3). pp. 310 - 310. ISSN: 0033-7587
Tosi, S., Giudici, G., Mosna, G., Harbott, J., Specchia, G., Grosveld, G., et al. (1998) 'Identification of new partner chromosomes involved in fusions with the ETV6 (TEL) gene in hematologic malignancies'. Genes Chromosomes and Cancer, 21 (3). pp. 223 - 229. ISSN: 1045-2257
Slijepcevic, P., Natarajan, AT. and Bryant, PE. (1998) 'Telomeres and radiation-induced chromosome breakage'. Mutagenesis, 13 (1). pp. 45 - 49. ISSN: 0267-8357
Payne, AM., Downes, SM., Bessant, DAR., Taylor, R., Holder, GE., Warren, MJ., et al. (1998) 'A mutation in guanylate cyclase activator 1A(GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1'. Human Molecular Genetics, 7 (2). pp. 273 - 277. ISSN: 0964-6906
Bridger, JM. and Bickmore, WA. (1998) 'Putting the genome on the map'. Trends in Genetics, 14 (10). pp. 403 - 409. ISSN: 0168-9525 Open Access Link