CenGEM
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
Hopwood, P., Harvey, A., Davies, J., Stephens, RJ., Girling, DJ., Gibson, D., et al. (1998) 'Survey of the administration of quality of life (QL) questionnaires in three multicentre randomised trials in cancer'. European Journal of Cancer, 34 (1). pp. 49 - 57. ISSN: 0959-8049
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
Forbes, SJ., Themis, M., Alison, MR., Selden, C., Coutelle, C. and Hodgson, HJF. (1998) 'Retroviral gene transfer to the liver in vivo during tri-iodothyronine induced hyperplasia'. Gene Therapy, 5 (4). pp. 552 - 555. ISSN: 0969-7128
Bridger, JM., Kill, IR. and Lichter, P. (1998) 'Association of pKi-67 with satellite DNA of the human genome in early G(1) cells'. Chromosome Research, 6 (1). pp. 13 - 24. ISSN: 0967-3849
King, JA., Bridger, JM., Gounari, F., Lichter, P., Schulz, TF., Schirrmacher, V. and et al. (1998) 'The extended packaging sequence of MoMLV contains a constitutive mRNA nuclear export function'. FEBS Letters, 434 (3). pp. 367 - 371. ISSN: 0014-5793
Weber, RG., Bridger, JM., Benner, A., Weisenberger, D., Ehemann, V., Reifenberger, G. and et al. (1998) 'Centrosome amplification as a possible mechanism for numerical chromosome aberrations in cerebral primitive neuroectodermal tumors with TP53 mutations'. Cytogenet Cell Genetics, 83 (3-4). pp. 266 - 269. ISSN: 0301-0171 Open Access Link
Bridger, JM., Herrmann, H., Muenkel, C. and Lichter, P. (1998) 'Identification of an interchromosomal compartment by polymerization of nuclear-targeted vimentin'. Journal of Cell Science, 111 (9). pp. 1241 - 1253. ISSN: 0021-9533 Open Access Link
Papaioannou, M., Bessant, D., Payne, A., Bellingham, J., Rougas, C., Loutradis-Anagnostou, A., et al. (1998) 'A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q'. Journal of Medical Genetics, 35 (5). pp. 429 - 431. ISSN: 0022-2593
Roberts, T., Chernova, O. and Cowell, JK. (1998) 'Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)'. Cancer Genetics and Cytogenetics, 100 (1). pp. 10 - 20. ISSN: 0165-4608
Bessant, DAR., Khaliq, S., Hameed, A., Anwar, K., Mehdi, SQ., Payne, AM. and et al. (1998) 'A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32'. American Journal of Human Genetics, 62 (5). pp. 1113 - 1116. ISSN: 0002-9297
Bessant, DAR., Payne, AM., Plant, C., Bird, AC. and Bhattacharya, SS. (1998) 'Further refinement of the Usher 2A locus at 1q41'. Journal of Medical Genetics, 35 (9). pp. 773 - 774. ISSN: 0022-2593
Payne, AM., Downes, SM., Bessant, DAR., Bird, AC. and Bhattacharya, SS. (1998) 'Founder effect, seen in the British population, of the 172 peripherin/RDS mutation- and further refinement of genetic positioning of the peripherin/RDS gene [2]'. American Journal of Human Genetics, 62 (1). pp. 192 - 195. ISSN: 0002-9297
Sokal, I., Li, N., Surgucheva, I., Warren, MJ., Payne, AM., Bhattacharya, SS., et al. (1998) 'GCAP1(Y99C) mutant is constitutively active in autosomal dominant cone dystrophy'. Molecular Cell, 2 (1). pp. 129 - 133. ISSN: 1097-2765
Slijepcevic, P., Hande, MP., Bouffler, SD., Lansdorp, P. and Bryant, PE. (1997) 'Telomere length, chromatin structure and chromosome fusigenic potential'. Chromosoma, 106 (7). pp. 413 - 421. ISSN: 0009-5915
Tosi, S., Scherer, SW., Biondi, A., Giudici, G. and Kearney, L. (1997) 'Cryptic deletion in 7q22 associated with a t(7;7) defines a new commonly deleted segment in myeloid malignancies. (Abstract)'. W B Saunders co. pp. 292 - 292. ISSN: 0006-4971
Tosi, S., Scherer, SW., Biondi, A., Giudici, G. and Kearney, L. (1997) 'Cryptic deletion in 7q22 associated with a t(7;7) defines a new commonly deleted segment in myeloid malignancies'. Blood, 90 (10). pp. 292 - 292. ISSN: 0006-4971
Kortenkamp, A., Jones, C. and Baker, J. (1997) 'Genotypic selection of mutated DNA sequences using mismatch cleavage analysis, a possible basis for novel mutation assays'. Mutagenesis, 12 (5). pp. 335 - 338. ISSN: 0267-8357
Lampel, S., Bridger, JM., Zirbel, R., Mathieu, U. and Lichter, P. (1997) 'Nuclear RNA accumulations represent released transcripts and exhibit specific distributions with respect to Sm antigens domains'. DNA and Cell Biology, 16 (10). pp. 1133 - 1142. ISSN: 1044-5498 Open Access Link
Payne, AM., Downes, SM., Bessant, DAR., Taylor, R., Fitzke, FW., Holder, G., et al. (1997) 'New locus for autosomal dominant cone dystrophy mapping to 6p21.1.'. CELL PRESS. pp. A290 - A290. ISSN: 0002-9297
Wilmen, A., Strowski, M., Hofken, T., Fuller, P., Printz, H., Goke, B. and et al. (1997) 'Differential display analysis reveals differential regulation of pancreatic genes during experimental pancreatitis'. GUT. pp. A75 - A75. ISSN: 0017-5749
Douar, AM., Adebakin, S., Themis, M., Pavirani, A., Cook, T. and Coutelle, C. (1997) 'Foetal gene delivery in mice by intra-amniotic administration of retroviral producer cells and adenovirus'. Gene Therapy, 4 (9). pp. 883 - 890. ISSN: 0969-7128
Still, IH., Roberts, T. and Cowell, JK. (1997) 'Fine structure physical mapping of a 1 center dot 9 Mb region of chromosome 13q12 (vol 61, pg 15, 1997)'. ANNALS OF HUMAN GENETICS, 61. pp. 379 - 379. ISSN: 0003-4800
Tosi, S., Harbott, J., Cazzaniga, G., Giudici, G., Biondi, A., Scherer, SW. and et al. (1997) 'Translocations involving the TEL/ETV6 region on 12p13 and at least two different regions on 7q'. Karger. pp. 344 - 344. ISSN: 0301-0171
Still, IH., Roberts, T. and Cowell, JK. (1997) 'Fine structure physical mapping of a 1.9 Mb region of chromosome 13q12'. Annals of Human Genetics, 61 (1). pp. 15 - 24. ISSN: 0003-4800
Downes, SM., Payne, AM., Bessant, DAR., Fitzke, FW., Holder, GE., Bhattcharya, SS. and et al. (1997) 'The RDS 172 mutation shows a common phenotype in twelve different families'. Investigative Ophthalmology and Visual Science, 38 (4). pp. 3707 - 3707. ISSN: 1552-5783
Bessant, DAR., Payne, AM., Downes, SM., Fitzke, FW., Holder, GE., Bhattacharya, SS. and et al. (1997) 'Rhodopsin mutations in sectorial retinitis pigmentosa.'. Investigative Ophthalmology and Visual Science, 38 (4). pp. 3712 - 3712. ISSN: 1552-5783
Payne, AM., Upadhyaya, VJ., Bessant, DAR., Downes, SM., Fitzke, FW., Holder, GE., et al. (1997) 'The characterisation and effect of myosin VIIa mutations in patients with Usher syndrome type I'. Investigative Ophthalmology and Visual Science, 38 (4). pp. 3719 - 3719. ISSN: 1552-5783
Payne, AM., Downes, SM., Bessant, DAR., Taylor, R., Fitzke, FW., Holder, GE., et al. (1997) 'New locus for autosomal dominant cone dystrophy mapping to 6p21.1'. American Journal of Human Genetics, 61 (4). pp. 1693 - 1693. ISSN: 1537-6605
Papaioannou, MG., Payne, AM., Bessant, D., Moschos, M., Loutradi Anagnostou, A., Balassopoulou, A. and et al. (1997) 'Homozygosity mapping of a consanguineous Greek family with autosomal recessive cone-rod dystrophy.'. American Journal of Human Genetics, 61 (4). pp. 2407 - 2407. ISSN: 1537-6605
Tosi, S., Mosna, G., Cazzaniga, G., Giudici, G., Kearney, L., Biondi, A. and et al. (1997) 'Unbalanced t(3;12) in a case of juvenile myelomonocytic leukemia (JMML) results in partial trisomy of 3q as defined by FISH'. Leukemia, 11 (9). pp. 1465 - 1468. ISSN: 0887-6924
Roberts, T. and Cowell, JK. (1997) 'Cloning of the human Gfi-1 gene and its mapping to chromosome region 1p22'. Oncogene, 14 (8). pp. 1003 - 1005. ISSN: 0950-9232
Kortenkamp, A. (1997) 'Problems in the biological monitoring of chromium(VI) exposed individuals'. Biomarkers, 2 (2). pp. 73 - 79. ISSN: 1354-750X
Slijepcevic, P. and Bryant, PE. (1997) 'Telomere-mediated chromosome healing.'. Radiation Research, 148 (3). pp. 293. ISSN: 0033-7587
Slijepcevic, P., Xiao, Y., Natarajan, AT. and Bryant, PE. (1997) 'Instability of cho chromosomes containing interstitial telomeric sequences originating fromchinese hamster chromosome 10'. Cytogenetics and Cell Genetics, 76 (1-2). pp. 58 - 60. ISSN: 0301-0171
Natarajan, AT., Balajee, AS., Boei, JJWA., Darroudi, F., Dominguez, I., Hande, MP., et al. (1996) 'Mechanisms of induction of chromosomal aberrations and their detection by fluorescence in situ hybridization'.26th Meeting of the European-Environmental-Mutagen-Society. ROME, ITALY. 1 - 7 September. Elsevier BV. pp. 247 - 258. ISSN: 0027-5107
Douar, AM., Themis, M., Sandig, V., Friedmann, T. and Coutelle, C. (1996) 'Effect of amniotic fluid on cationic lipid mediated transfection and retroviral infection'. Gene Therapy, 3 (9). pp. 789 - 796. ISSN: 0969-7128
Douar, AM., Themis, M. and Coutelle, C. (1996) 'Fetal somatic gene therapy'. Molecular Human Reproduction, 2 (9). pp. 633 - 641. ISSN: 1360-9947
Roberts, T., Auffray, C. and Cowell, JK. (1996) 'Regional localization of 192 genic markers on human chromosome 1'. Genomics, 36 (2). pp. 337 - 340. ISSN: 0888-7543
Tosi, S., Cabot, G., Giudici, G., Attuati, V., Morandi, P., Rambaldi, A., et al. (1996) 'Detection of the breakpoint cluster region-ABL fusion in chronic myeloid leukemia with variant Philadelphia chromosome translocations by in situ hybridization'. Cancer Genetics and Cytogenetics, 89 (2). pp. 153 - 156. ISSN: 0165-4608