CenGEM
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
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
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
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
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
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
Kortenkamp, A. (1997) 'Problems in the biological monitoring of chromium(VI) exposed individuals'. Biomarkers, 2 (2). pp. 73 - 79. ISSN: 1354-750X
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
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
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
Kortenkamp, A. (1996) 'Pharmacokinetic modelling in chromium risk assessment - A prediction of chromium (III) accumulation in humans from chromium dietary supplements - Comment'. HUMAN & EXPERIMENTAL TOXICOLOGY, 15 (7). pp. 601 - 602. ISSN: 0144-5952
Kortenkamp, A., Casadevall, M., DaCruzFresco, P. and Shayer, ROJ. (1996) 'Pathways in the chromium(VI)-mediated formation of DNA lesions: A review'.NATO Advanced Study Institute on Cytotoxic, Mutagenic and Carcinogenic Potential of Heavy Metals Related to Human Environment. PRZESIEKA, POLAND. 15 - 26 June. KLUWER ACADEMIC PUBL. pp. 15 - 34.
Kortenkamp, A. (1996) 'Approaches to the biological monitoring of chromium(VI) exposed individuals'.NATO Advanced Study Institute on Cytotoxic, Mutagenic and Carcinogenic Potential of Heavy Metals Related to Human Environment. PRZESIEKA, POLAND. 15 - 26 June. KLUWER ACADEMIC PUBL. pp. 35 - 53.
Raimondi, E., Balzaretti, M., Moralli, D., Vagnarelli, P., Tredici, F., Bensi, M. and et al. (1996) 'Gene targeting to the centromeric DNA of a human minichromosome'. Human Gene Therapy, 7 (9). pp. 1103 - 1109. ISSN: 1043-0342
Slijepcevic, P., Xiao, Y., Dominguez, I. and Natarajan, AT. (1996) 'Spontaneous and radiation-induced chromosomal breakage at interstitial telomeric sites'. Chromosoma, 104 (8). pp. 596 - 604. ISSN: 0009-5915
Kortenkamp, A., Casadevall, M., Faux, SP., Jenner, A., Shayer, ROJ., Woodbridge, N. and et al. (1996) 'A role for molecular oxygen in the formation of DNA damage during the reduction of the carcinogen chromium(VI) by glutathione'. Archives of Biochemistry and Biophysics, 329 (2). pp. 199 - 207. ISSN: 0003-9861
ROBERTS, T., MEAD, RS. and COWELL, JK. (1996) 'Characterisation of a human chromosome 1 somatic cell hybrid mapping panel and regional assignment of 6 novel STS'. Annals of Human Genetics, 60 (3). pp. 213 - 220. ISSN: 0003-4800
Still, IH., Roberts, T., Bia, B., Hawthorn, L., Auffray, C. and Cowell, J. (1996) 'Incorporation of 35 novel gene transcripts into the physical and genetic map of human chromosome 13'. Genomics, 33 (2). pp. 159 - 166. ISSN: 0888-7543
Kortenkamp, A., Casadevall, M. and Da Cruz Fresco, P. (1996) 'The reductive conversion of the carcinogen chromium (VI) and its role in the formation of DNA lesions'. Annals of Clinical and Laboratory Science, 26 (2). pp. 160 - 175. ISSN: 0091-7370
Payne, AM., Evans, K., Plant, C., Bird, AC. and Bhattacharya, SS. (1996) 'The prevalence and effect of peripherin/RDS mutations in autosomal dominant pattern dystrophy'. Investigative Ophthalmology and Visual Science, 37 (3). pp. 508 - 508. ISSN: 0146-0404
Bouffler, SD., Morgan, WF., Pandita, TK. and Slijepcevic, P. (1996) 'The involvement of telomeric sequences in chromosomal aberrations'. Mutation Research - Reviews in Genetic Toxicology, 366 (2). pp. 129 - 135. ISSN: 0165-1110
Xiao, Y., Slijepcevic, P., Arkesteijn, G., Darroudi, F. and Natarajan, AT. (1996) 'Development of DNA libraries specific for Chinese hamster chromosomes 3, 4, 9, 10, X, and Y by DOP-PCR'. Cytogenetics and Cell Genetics, 75 (1). pp. 57 - 62. ISSN: 0301-0171
Tosi, S., Harbott, J., Haas, OA., Douglas, A., Hughes, DM., Ross, FM., et al. (1996) 'Classification of deletions and identification of cryptic translocations involving 7q by fluoresence in situ hybridization (FISH)'. Leukemia, 10 (4). pp. 644 - 649. ISSN: 0887-6924
Kortenkamp, A. (1996) 'Pharmacokinetic modelling in chromium risk assessment.'. Human & experimental toxicology, 15 (7). pp. 601 - 602. ISSN: 0960-3271
Roberts, T., Mead, RS. and Well, JKCO. (1996) 'Characterisation of a human chromosome 1 somatic cell hybrid mapping panel and regional assignment of 6 novel STS'. Annals of Human Genetics, 60 (3). pp. 213 - 220. ISSN: 0003-4800
Makarova, OV., Makarov, EM., Sousa, R. and Dreyfus, M. (1995) 'Transcribing of Escherichia coli genes with mutant T7 RNA polymerases: stability of lacZ mRNA inversely correlates with polymerase speed.'. Proceedings of the National Academy of Sciences, 92 (26). pp. 12250 - 12254. ISSN: 0027-8424
Hawthorn, L., Roberts, T., Verlind, E., Kooy, RF. and Cowell, JK. (1995) 'A yeast artificial chromosome contig that spans the RB1-D13S31 interval on human chromosome 13 and encompasses the frequently deleted region in B-cell chronic lymphocytic leukemia'. Genomics, 30 (3). pp. 425 - 430. ISSN: 0888-7543
O'Brien, P. and Kortenkamp, A. (1995) 'The chemistry underlying chromate toxicity'. Transition Metal Chemistry, 20 (6). pp. 636 - 642. ISSN: 0340-4285
Tosi, S., Harbott, J., Haas, QA., Douglas, A., Hughes, D., Ross, F., et al. (1995) 'Molecular cytogenetic analysis of 7q deletions in haematological malignancies. (Abstract)'. W B SAUNDERS CO. pp. 2965 - 2965. ISSN: 0006-4971
Natarajan, AT., Boei, JJWA. and Slijepcevic, P. (1995) 'Use of telomeric probing in identifying radiation induced chromosomal aberrations'.10th International Congress of Radiation Research (10th ICRR) - Radiation Research 1895-1995. WURZBURG, GERMANY. 27 - 1 September. 10TH ICRR SOCIETY (INT CONGRESS RADIATION RES). pp. 489 - 492.
Slijepcevic, P. and Natarajan, AT. (1995) 'Fragile site at Xq21 in Chinese hamster and its implications for the in vitro chromosomal aberration test'. Mutagenesis, 10 (4). pp. 353 - 355. ISSN: 0267-8357
O'Brien, P., Jones, C. and Kortenkamp, A. (1995) 'Reactive chromium species potentially generated by welding fume'. Toxicological & Environmental Chemistry, 49 (3). pp. 149 - 155. ISSN: 0277-2248
Trott, DA., Cuthbert, AP., Todd, CM., Themis, M. and Newbold, RF. (1995) 'Novel use of a selectable fusion gene as an "in-out" marker for studying genetic loss in mammalian cells'. Molecular Carcinogenesis, 12 (4). pp. 213 - 224. ISSN: 0899-1987
Hashim, Y., Ragoussis, I., Kearney, L., Tosi, S. and So, AK. (1995) 'Physical mapping of the human T-Cell Receptor-Beta Gene-Complex, using yeast artificial Chromosomes'. IMMUNOGENETICS, 41 (6). pp. 337 - 342. ISSN: 0093-7711
Casadevall, M. and Kortenkamp, A. (1995) 'The formation of both apurinic/apyrimidinic sites and single-strand breaks by chromate and glutathione arises from attack by the same single reactive species and is dependent on molecular oxygen'. Carcinogenesis, 16 (4). pp. 805 - 809. ISSN: 0143-3334
Kempski, H., MacDonald, D., Michalski, AJ., Roberts, T., Goldman, JM., Cross, NCP. and et al. (1995) 'Localization of the 8-13 translocation breakpoint associated with myeloproliferative disease to a 1.5 mbp region of chromosome-13'. Genes Chromosomes and Cancer, 12 (4). pp. 283 - 287. ISSN: 1045-2257
RAIMONDI, E., MORALLI, D., VAGNARELLI, P., BALZARETTI, M. and DECARLI, L. (1995) 'HUMAN MINICHROMOSOMES AS POTENTIAL VECTORS FOR GENE-THERAPY'.41st International Congress of the European-Tissue-Culture-Society. VERONA, ITALY. 1 - 12 October. BIOMED CENTRAL LTD. pp. 207 - 209. ISSN: 1756-9966
Cuthbert, AP., Trott, DA., Ekong, RM., Jezzard, S., England, NL., Themis, M., et al. (1995) 'Construction and characterization of a highly stable human:Rodent monochromosomal hybrid panel for genetic complementation and genome mapping studies'. Cytogenetics and Cell Genetics, 71 (1). pp. 68 - 76. ISSN: 0301-0171
Hashim, Y., Ragoussis, I., Kearney, L., Tosi, S. and Ak, SO. (1995) 'Physical mapping of the human T-Cell antigen receptor Beta-Gene complex using yeast artificial chromosomes (Abstract)'. KARGER. pp. 24 - 25. ISSN: 0301-0171
Slijepcevic, P. and Bryant, PE. (1995) 'Absence of terminal telomeric FISH signals in chromosomes from immortal Chinese hamster cells'. Cytogenetics and Cell Genetics, 69 (1-2). pp. 87 - 89. ISSN: 0301-0171
Tosi, S., Scherer, SW., Rambaldi, A., Hashim, Y., Wainscoat, JS., Osborne, L., et al. (1995) 'Characterization of 7Q Abnormalities in the human Myeloid-Leukemia Cell-Line GFD8 by fluorescence in-situ hybridization (FISH) (Abstract)'. KARGER. pp. 28 - 28. ISSN: 0301-0171