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
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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.
- Page last reviewed:Feb 1, 2024
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