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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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Conference paper

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

Journal article

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

Journal article

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

Conference paper

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

Conference paper

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

Journal article

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

Journal article

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

Journal article

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

Journal article

Slijepcevic, P. and Bryant, PE. (1997) 'Telomere-mediated chromosome healing.'. Radiation research, 148 (3). pp. 293. ISSN: 0033-7587

Journal article

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

Conference paper

Kortenkamp, A. (1997) 'Problems in the biological monitoring of chromium(VI) exposed individuals'. Biomarkers, 2 (2). pp. 73 - 79. ISSN: 1354-750X

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Conference paper

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

Journal article

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

Journal article

Douar, AM., Themis, M. and Coutelle, C. (1996) 'Fetal somatic gene therapy'. Molecular Human Reproduction, 2 (9). pp. 633 - 641. ISSN: 1360-9947

Journal article

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

Journal article

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

Journal article

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.

Conference paper

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.

Conference paper

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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

Journal article

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