Extended-term cultures of human T-lymphocytes: a practical alternative to primary human lymphocytes for use in genotoxicity testing.

PubWeight™: 0.84‹?›

🔗 View Article (PMID 7666770)

Published in Mutagenesis on May 01, 1995

Authors

M R O'Donovan1, M R Freemantle, G Hull, D A Bell, C F Arlett, J Cole

Author Affiliations

1: Research Department, Boots Pharmaceuticals, Nottingham, UK.

Articles by these authors

A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science (1995) 15.20

Terminal restriction fragment length polymorphism analysis program, a web-based research tool for microbial community analysis. Appl Environ Microbiol (2000) 5.54

Short tandem repeat profiling provides an international reference standard for human cell lines. Proc Natl Acad Sci U S A (2001) 4.84

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity. Nature (1975) 4.30

Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation. Proc Natl Acad Sci U S A (1975) 4.02

Nomenclature for N-acetyltransferases. Pharmacogenetics (1995) 3.59

The role of the CYP2C9-Leu359 allelic variant in the tolbutamide polymorphism. Pharmacogenetics (1996) 3.02

Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient. Curr Biol (1999) 2.98

Human glutathione S-transferase P1 polymorphisms: relationship to lung tissue enzyme activity and population frequency distribution. Carcinogenesis (1998) 2.65

Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophy. J Invest Dermatol (1990) 2.31

Low-cost high-resolution fast spin-echo MR of acoustic schwannoma: an alternative to enhanced conventional spin-echo MR? AJNR Am J Neuroradiol (1996) 2.24

XRCC1 polymorphisms: effects on aflatoxin B1-DNA adducts and glycophorin A variant frequency. Cancer Res (1999) 2.21

Galactose consumption and metabolism in relation to the risk of ovarian cancer. Lancet (1989) 2.20

XPD polymorphisms: effects on DNA repair proficiency. Carcinogenesis (2000) 2.16

Exclusive elemental diet impacts on the gastrointestinal microbiota and improves symptoms in patients with chronic pouchitis. J Crohns Colitis (2012) 2.00

Molecular analysis of ouabain-resistant mutants of the mouse lymphoma cell line L5178Y. Mutagenesis (1987) 2.00

p53 gene mutations and protein accumulation in human ovarian cancer. Proc Natl Acad Sci U S A (1993) 1.93

An association between the allele coding for a low activity variant of catechol-O-methyltransferase and the risk for breast cancer. Cancer Res (1997) 1.92

Mutation of K-ras protooncogene in human ovarian epithelial tumors of borderline malignancy. Cancer Res (1993) 1.89

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene. Proc Natl Acad Sci U S A (1997) 1.87

The biogenesis of c-type cytochromes in Escherichia coli requires a membrane-bound protein, DipZ, with a protein disulphide isomerase-like domain. Mol Microbiol (1995) 1.84

Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene. Nucleic Acids Res (1992) 1.83

Increased risk for myelodysplastic syndromes in individuals with glutathione transferase theta 1 (GSTT1) gene defect. Lancet (1996) 1.81

Nucleotide sequence, organisation and structural analysis of the products of genes in the nirB-cysG region of the Escherichia coli K-12 chromosome. Eur J Biochem (1990) 1.66

Molecular evidence for multifocal papillary serous carcinoma of the peritoneum in patients with germline BRCA1 mutations. J Natl Cancer Inst (1998) 1.64

Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3. Am J Hum Genet (1994) 1.64

Systematic review: the effect of prunes on gastrointestinal function. Aliment Pharmacol Ther (2014) 1.62

Serologic subsets in systemic lupus erythematosus: an examination of autoantibodies in relationship to clinical features of disease and HLA antigens. Arthritis Rheum (1980) 1.62

Whole genome amplification and high-throughput allelotyping identified five distinct deletion regions on chromosomes 5 and 6 in microdissected early-stage ovarian tumors. Cancer Res (2001) 1.61

Organization of kappa light chain genes in germ-line and somatic tissue. Proc Natl Acad Sci U S A (1980) 1.61

Possible association between mutant frequency in peripheral lymphocytes and domestic radon concentrations. Lancet (1991) 1.59

Catechol-O-methyltransferase and breast cancer risk. Carcinogenesis (1998) 1.58

Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome. Cold Spring Harb Symp Quant Biol (1994) 1.57

Serum concentrations of organochlorine compounds and the subsequent development of breast cancer. Cancer Epidemiol Biomarkers Prev (1999) 1.57

The calculation of target height reconsidered. Horm Res (2003) 1.56

Escherichia coli K-12 genes essential for the synthesis of c-type cytochromes and a third nitrate reductase located in the periplasm. Mol Microbiol (1996) 1.52

The influence of lactose consumption on the association of oral contraceptive use and ovarian cancer risk. Am J Epidemiol (1991) 1.52

A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy. Am J Hum Genet (1993) 1.51

The development of rheumatoid arthritis after recombinant hepatitis B vaccination. J Rheumatol (1998) 1.50

Identification of a novel 9 cM deletion unit on chromosome 6q23-24 in papillary serous carcinoma of the peritoneum. Hum Pathol (2000) 1.48

Survey of radiosensitivity in a variety of human cell strains. Cancer Res (1980) 1.46

Molecular cloning and functional analysis of the cysG and nirB genes of Escherichia coli K12, two closely-linked genes required for NADH-dependent nitrite reductase activity. Mol Gen Genet (1985) 1.46

Vitamin D levels in women with systemic lupus erythematosus and fibromyalgia. J Rheumatol (2001) 1.46

A comparison of the 8-azaguanine and ouabain-resistance systems for the selection of induced mutant Chinese hamster cells. Mutat Res (1975) 1.46

Differential expression of the Arabidopsis genes coding for Em-like proteins. J Exp Bot (2000) 1.45

A seventh complementation group in excision-deficient xeroderma pigmentosum. Mutat Res (1979) 1.45

The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation. Mutat Res (1975) 1.44

Transitional cell metaplasia of the uterine cervix and vagina: an underrecognized lesion that may be confused with high-grade dysplasia. A report of 59 cases. Am J Surg Pathol (1997) 1.44

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome. Am J Hum Genet (1995) 1.44

Underestimation of the small residual damage when measuring DNA double-strand breaks (DSB): is the repair of radiation-induced DSB complete? Int J Radiat Biol (1999) 1.43

Cigarette smoking, N-acetyltransferases 1 and 2, and breast cancer risk. Cancer Epidemiol Biomarkers Prev (1998) 1.43

Prognostic significance of DNA content in epithelial ovarian cancer. Gynecol Oncol (1994) 1.43

Human papillomavirus typing in patients with Papanicolaou smears showing squamous atypia. Gynecol Oncol (1993) 1.42

A seven-gene operon essential for formate-dependent nitrite reduction to ammonia by enteric bacteria. Mol Microbiol (1994) 1.42

A controlled study of the effects of a supervised cardiovascular fitness training program on the manifestations of primary fibromyalgia. Arthritis Rheum (1988) 1.40

Anti-DNA autoantibody-producing hybridomas of normal human lymphoid cell origin. J Clin Invest (1984) 1.40

Repair of ultraviolet light damage in a variety of human fibroblast cell strains. Cancer Res (1977) 1.40

GSTM1, GSTT1, GSTP1, CYP1A1, and NAT1 polymorphisms, tobacco use, and the risk of head and neck cancer. Cancer Epidemiol Biomarkers Prev (2000) 1.40

The influence of humidity, sunlight, and temperature on the daytime decay of polyaromatic hydrocarbons on atmospheric soot particles. Environ Sci Technol (1988) 1.39

Human disorders showing increased sensitivity to the induction of genetic damage. Annu Rev Genet (1978) 1.38

A global paleoclimate observing system. Science (2001) 1.38

Bcl-2 and p53 protein expression, apoptosis, and p53 mutation in human epithelial ovarian cancers. Am J Pathol (2000) 1.35

Polymorphisms in the DNA repair gene XRCC1 and breast cancer. Cancer Epidemiol Biomarkers Prev (2001) 1.35

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene. Hum Mol Genet (2001) 1.33

The nature and origin of mutations which block a temporal sequence for genic expression in paramecium. Genetics (1967) 1.32

Thrombosis of the deep venous drainage of the brain in adults. Analysis of seven cases with review of the literature. Arch Neurol (1995) 1.32

Two different Em-like genes are expressed in Arabidopsis thaliana seeds during maturation. Mol Gen Genet (1993) 1.29

V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder. J Biol Chem (1993) 1.29

Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia. Br J Cancer (1999) 1.29

Nitrate reduction in the periplasm of gram-negative bacteria. Adv Microb Physiol (2001) 1.28

Glutathione S-transferase GSTT1 genotypes and susceptibility to cancer: studies of interactions with GSTM1 in lung, oral, gastric and colorectal cancers. Carcinogenesis (1996) 1.28

The role of proprioception and attention in a visuomotor adaptation task. Exp Brain Res (2000) 1.28

Microsomal epoxide hydrolase polymorphism as a risk factor for ovarian cancer. Mol Carcinog (1996) 1.27

Clinical experience with trisomies 18 and 13. J Med Genet (1978) 1.27

Glutathione S-transferase genotype as a susceptibility factor in smoking-related coronary heart disease. Atherosclerosis (2000) 1.25

Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity. Hum Genet (1986) 1.25

ProbeDesigner: for the design of probesets for branched DNA (bDNA) signal amplification assays. Bioinformatics (1999) 1.23

Association of prostate cancer with vitamin D receptor gene polymorphism. Cancer Res (1996) 1.23

Production of human normal adult and fetal hemoglobins in Escherichia coli. Protein Eng (1997) 1.22

Glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) genetic polymorphism and susceptibility to gastric and colorectal adenocarcinoma. Carcinogenesis (1996) 1.22

Genetic family history questionnaire. J Med Genet (1978) 1.21

The NavChair Assistive Wheelchair Navigation System. IEEE Trans Rehabil Eng (1999) 1.21

Relationship between ambient air pollution and DNA damage in Polish mothers and newborns. Environ Health Perspect (1998) 1.20

The role of N-acetylation polymorphisms in smoking-associated bladder cancer: evidence of a gene-gene-exposure three-way interaction. Cancer Res (1998) 1.20

A DNA double-strand break defective fibroblast cell line (180BR) derived from a radiosensitive patient represents a new mutant phenotype. Cancer Res (1997) 1.19

Mitochondrial transport proteins of the brain. J Neurosci Res (2007) 1.19

Ethnic variation in the CYP2E1 gene: polymorphism analysis of 695 African-Americans, European-Americans and Taiwanese. Pharmacogenetics (1994) 1.19

Role of aromatic amine acetyltransferases, NAT1 and NAT2, in carcinogen-DNA adduct formation in the human urinary bladder. Cancer Res (1995) 1.19

The Escherichia coli cysG promoter belongs to the 'extended -10' class of bacterial promoters. Biochem J (1993) 1.18

Evaluation of amitriptyline in primary fibrositis. A double-blind, placebo-controlled study. Arthritis Rheum (1986) 1.18

Functional characterization of cyclooxygenase-2 polymorphisms. J Pharmacol Exp Ther (2001) 1.18

Effect of a developmental program on motor performance in infants born preterm. Aust J Physiother (2001) 1.17

Analysis of variable region genes encoding a human anti-DNA antibody of normal origin. Implications for the molecular basis of human autoimmune responses. J Immunol (1989) 1.17

Regulation and sequence of the structural gene for cytochrome c552 from Escherichia coli: not a hexahaem but a 50 kDa tetrahaem nitrite reductase. Mol Microbiol (1993) 1.17

A 400 kb novel deletion unit centromeric to the BRCA1 gene in sporadic epithelial ovarian cancer. Oncogene (1996) 1.16

Genetic variability in susceptibility and response to toxicants. Toxicol Lett (2001) 1.15

An essential role for DsbA in cytochrome c synthesis and formate-dependent nitrite reduction by Escherichia coli K-12. Arch Microbiol (1995) 1.13