Mutagen Sensitivity
What's New
Last Posted: May 31, 2023
- Assessment of genotoxic instability markers in peripheral blood lymphocytes of breast cancer patients: a case control study.
Smitha G Raj, et al. Journal of biomolecular structure & dynamics 2023 0 1-5 - The Role of Micronucleus Assay to Detect Genetic Instability in Respiratory Cancer Patients.
Bolognesi Claudia, et al. Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer 2020 0 (4) 345-352 - Investigations of potential susceptibility toward formaldehyde-induced genotoxicity.
Zeller Jasmin, et al. Archives of toxicology 2012 9 (9) 1465-73 - Association of Rad51 polymorphism with DNA repair in BRCA1 mutation carriers and sporadic breast cancer risk.
Ricks-Santi LJ, et al. BMC cancer 2011 6 (1) 1 - Mutagen sensitivity
From NCATS Genetic and Rare Diseases Information Center - A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity.
Gu Jian, et al. Human molecular genetics 2011 2 (4) 820-6 - Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk.
Liu Yanhong, et al. Carcinogenesis 2010 10 (10) 1762-9 - A comprehensive haplotype analysis of the XPC genomic sequence reveals a cluster of genetic variants associated with sensitivity to tobacco-smoke mutagens.
Rondelli Catherine M, et al. Toxicological sciences : an official journal of the Society of Toxicology 2010 5 (1) 41-50 - Association between common genetic variation in Cockayne syndrome A and B genes and nucleotide excision repair capacity among smokers.
Leng Shuguang, et al. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 8 (8) 2062-9 - Haplotypes of DNMT1 and DNMT3B are associated with mutagen sensitivity induced by benzo[a]pyrene diol epoxide among smokers.
Leng Shuguang, et al. Carcinogenesis 2008 7 (7) 1380-5 - Micronuclei frequency induced by bleomycin in human peripheral lymphocytes: correlating BLHX polymorphism with mutagen sensitivity.
Maffei Francesca, et al. Mutation research 2008 3 (1-2) 20-6 - Inherited susceptibility to bleomycin-induced micronuclei: correlating polymorphisms in GSTT1, GSTM1 and DNA repair genes with mutagen sensitivity.
Angelini Sabrina, et al. Mutation research 2008 2 (1-2) 90-7 - Mutagen sensitivity and genetic variants in nucleotide excision repair pathway: genotype-phenotype correlation.
Lin Jie, et al. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 10 (10) 2065-71 - 172G>T variant in the 5' untranslated region of DNA repair gene RAD51 reduces risk of squamous cell carcinoma of the head and neck and interacts with a P53 codon 72 variant.
Lu Jiachun, et al. Carcinogenesis 2007 5 (5) 988-94 - Bladder cancer predisposition: a multigenic approach to DNA-repair and cell-cycle-control genes.
Wu Xifeng, et al. American journal of human genetics 2006 3 (3) 464-79 - Evaluation of glutathione S-transferase polymorphisms and mutagen sensitivity as risk factors for the development of second primary tumors in patients previously diagnosed with early-stage head and neck cancer.
Minard Charles G, et al. Cancer 2006 6 (12) 2636-44 - Effect of XPD/ERCC2 polymorphisms on chromosome aberration frequencies in smokers and on sensitivity to the mutagenic tobacco-specific nitrosamine NNK.
Affatato Alessandra A, et al. Environmental and molecular mutagenesis 2004 0 (1) 65-73 - Gender differences in genetic damage induced by the tobacco-specific nitrosamine NNK and the influence of the Thr241Met polymorphism in the XRCC3 gene.
Hill Courtney E, et al. Environmental and molecular mutagenesis 2005 7 (1) 22-9 - Genetic polymorphisms in the base excision repair pathway and cancer risk: a HuGE review.
Hung Rayjean J, et al. American journal of epidemiology 2005 11 (10) 925-42 - The L84F and the I143V polymorphisms in the O6-methylguanine-DNA-methyltransferase (MGMT) gene increase human sensitivity to the genotoxic effects of the tobacco-specific nitrosamine carcinogen NNK.
Hill Courtney E, et al. Pharmacogenetics and genomics 2005 8 (8) 571-8
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
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