A. Cuthbert

发表

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

E. Shoubridge, M. Chevrette, J. Yao, 1998, Nature Genetics.

Chromosome 17p13.2 transfer reverts transformation phenotypes and fas‐mediated apoptosis in breast epithelial cells

J. Russo, J. Testa, G. Mor, 2004, Molecular carcinogenesis.

Transfer of chromosome 8 into two breast cancer cell lines: total exclusion of three regions indicates location of putative in vitro growth suppressor genes.

G. Chenevix-Trench, A. Marsh, D. Purdie, 2003, Cancer genetics and cytogenetics.

Telomerase repressor sequences on chromosome 3 and induction of permanent growth arrest in human breast cancer cells.

C. Cooper, J. Bond, E. K. Parkinson, 1999, Journal of the National Cancer Institute.

Localization of a novel tumor metastasis suppressor region on the short arm of human chromosome 2

K. Miura, T. Mashimo, M. Watabe, 2000, Genes, chromosomes & cancer.

Identification of human tumour suppressor genes by monochromosome transfer: rapid growth-arrest response mapped to 9p21 is mediated solely by the cyclin-D-dependent kinase inhibitor gene, CDKN2A (p16INK4A).

D. Carson, S. Jezzard, T. Nobori, 1996, Carcinogenesis.

Cell immortalization as a key, rate-limiting event in malignant transformation: approaches toward a molecular genetic analysis.

M. Themis, A. Cuthbert, R. Newbold, 1993, Toxicology letters.

Genetic Variation at the Chromosome 16 Chemokine Gene Cluster: Development of a Strategy for Association Studies in Complex Disease

S. Fisher, A. Forbes, C. Lewis, 2003, Annals of human genetics.

Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15

S. Fisher, A. Forbes, Clive M. Onnie, 2006, Human mutation.

Corneodesmosin (CDSN) gene association with psoriasis vulgaris in Caucasian but not in Japanese populations

S. Fisher, C. M. Lewis, H. Nakagawa, 2005, Clincal and Experimental Dermatology.

A Crohn's disease‐associated insertion polymorphism (3020insC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo‐plantar pustular psoriasis or guttate psoriasis

C. Mathew, R. Trembath, A. Burden, 2003, Experimental dermatology.

Human chromosome 21 determines growth factor dependence in human/mouse B-cell hybridomas.

L. Aarden, A. Cuthbert, R. Newbold, 1998, Cancer research.

Human squamous cell carcinomas lose a mortality gene from chromosome 6q14.3 to q15

N. Barr, H. Ireland, E. Parkinson, 2003, Oncogene.

Human chromosome 16 suppresses metastasis but not tumorigenesis in rat prostatic tumor cells.

T. Mashimo, M. Watabe, K. Watabe, 1998, Cancer research.

hMSH6 deficiency and inactivation of the αE-catenin invasion-suppressor gene in HCT-8 colon cancer cells

F. Speleman, M. Mareel, F. van Roy, 2004, Clinical & Experimental Metastasis.

Functional evidence of novel tumor suppressor genes for cutaneous malignant melanoma.

D. Griffin, C. Parris, A. Cuthbert, 1999, Cancer research.

A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.

T. Hudson, A. Verner, D. González-Halphen, 2001, American journal of human genetics.

Human acrocentric chromosomes with transcriptionally silent nucleolar organizer regions associate with nucleoli

W. Bickmore, J. Bridger, B. McStay, 2001, The EMBO journal.

Novel use of a selectable fusion gene as an “In‐Out” marker for studying genetic loss in mammalian cells

M. Themis, A. Cuthbert, R. Newbold, 1995, Molecular carcinogenesis.

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

S. Fisher, C. Lewis, C. Mathew, 2001, The Lancet.

Genetic association between EPHX1 and Crohn’s disease: population stratification, genotyping error, or random chance?

S. Fisher, A. Forbes, C. Lewis, 2004, Gut.

Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15.

S. Fisher, C. Lewis, C. Mathew, 2003, Rheumatology.

A chromosome 3-encoded repressor of the human telomerase reverse transcriptase (hTERT) gene controls the state of hTERT chromatin.

J. Lingner, M. Nabholz, A. Cuthbert, 2003, Cancer research.

Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p

K. Huse, C. Mathew, J. Hampe, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Identification of tumor metastasis suppressor region on the short arm of human chromosome 20

K. Miura, T. Mashimo, M. Watabe, 2001, Genes, chromosomes & cancer.

Construction and characterization of a highly stable human: rodent monochromosomal hybrid panel for genetic complementation and genome mapping studies.

R. Ekong, S. Jezzard, M. Themis, 1995, Cytogenetics and cell genetics.

Telomere length abnormalities in mammalian radiosensitive cells.

M. Blasco, S. Bouffler, A. Riches, 2001, Cancer research.

Mechanisms involved in the immortalization of mammalian cells by ionizing radiation and chemical carcinogens.

A. Cuthbert, R. Newbold, I. Russo, 1995, Carcinogenesis.

the State of hTERT Chromatin ) Gene Controls hTERT ( Telomerase Reverse Transcriptase Human A Chromosome 3-encoded Repressor of the Updated Version

J. Lingner, M. Nabholz, A. Cuthbert, 2003 .

Functional evidence for a squamous cell carcinoma mortality gene(s) on human chromosome 4

N. Forsyth, N. Barr, H. Ireland, 2002, Oncogene.

Regulation of human telomerase activity: repression by normal chromosome 3 abolishes nuclear telomerase reverse transcriptase transcripts but does not affect c-Myc activity.

A. Ducrest, M. Amacker, J. Lingner, 2001, Cancer research.

Telomerase suppression by chromosome 6 in a human papillomavirus type 16-immortalized keratinocyte cell line and in a cervical cancer cell line.

C. Meijer, J. Walboomers, R. Steenbergen, 2001, Journal of the National Cancer Institute.

Transcriptase Transcripts but Does Not Affect c-Myc Activity ReverseNormal Chromosome 3 Abolishes Nuclear Telomerase Regulation of Human Telomerase Activity : Repression by Updated Version

A. Ducrest, M. Amacker, J. Lingner, 2001 .

A telomere-independent senescence mechanism is the sole barrier to Syrian hamster cell immortalization

D. Griffin, A. Silver, A. Cuthbert, 1998, Oncogene.

A mortality gene(s) for the human adenocarcinoma line HeLa maps to a 130-kb region of human chromosome 4q22-q23.

N. Forsyth, H. Ireland, V. Morrison, 2002, Neoplasia.

Similar regions of human chromosome 3 are eliminated from or retained in human/human and human/mouse microcell hybrids during tumor growth in severe combined immunodeficient (SCID) mice.

G. Klein, M. Kost-Alimova, S. Ingvarsson, 2001, Proceedings of the National Academy of Sciences of the United States of America.

The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomes.

M. Oshimura, Y. Shiloh, G. Verhaegh, 1996, Mutation research.

Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.

S. Fisher, A. Forbes, C. Lewis, 2003, American journal of human genetics.

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease.

Alastair Forbes, Christopher G Mathew, Jochen Hampe, 2002, Gastroenterology.

SNP Subset Selection for Genetic Association Studies

J. Whittaker, A. Cuthbert, M. C. Byng, 2003, Annals of human genetics.

Genetic and functional analyses exclude mortality factor 4 (MORF4) as a keratinocyte senescence gene.

M. J. Bertram, O. Pereira-smith, N. Forsyth, 1999, Cancer research.

Sequence variation in the CARD15 (NOD2) gene and susceptibity to Crohn's disease

S. Fisher, A. Forbes, J. Sanderson, 2003 .

Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel disease.

S. Fisher, A. Forbes, C. Lewis, 2003, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.

S. Fisher, C. Mathew, P. Rosenstiel, 2007, Genomics.