Genetic Variations in Xenobiotic Metabolic Pathway Genes, Personal Hair Dye Use, and Risk of Non-Hodgkin Lymphoma-Reference-Cited by-同舟云学术

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Genetic Variations in Xenobiotic Metabolic Pathway Genes, Personal Hair Dye Use, and Risk of Non-Hodgkin Lymphoma

Published:2009-10-12 Issue:10 Volume:170 Page:1222-1230
ISSN:0002-9262
Container-title:American Journal of Epidemiology
language:en
Short-container-title:American Journal of Epidemiology

Author:

Zhang Y.,Hughes K. J.,Zahm S. H.,Zhang Y.,Holford T. R.,Dai L.,Bai Y.,Han X.,Qin Q.,Lan Q.,Rothman N.,Zhu Y.,Leaderer B.,Zheng T.

Publisher

Oxford University Press (OUP)

Subject

Epidemiology

Link

http://academic.oup.com/aje/article-pdf/170/10/1222/261676/kwp263.pdf

Reference34 articles.

1. Association between Personal Use of Hair Dyes and Lymphoid Neoplasms in Europe

2. Hair dye use, genetic variation in N-acetyltransferase 1 (NAT1) and 2 (NAT2), and risk of non-Hodgkin lymphoma

3. Hair-coloring Product Use and Risk of Non-Hodgkin's Lymphoma: A Population-based Case-Control Study in Connecticut

4. Personal Use of Hair Dye and the Risk of Certain Subtypes of Non-Hodgkin Lymphoma

5. Hair dyes are mutagenic: identification of a variety of mutagenic ingredients.

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association between hair dye use and cancer in women: a systematic review and meta-analysis of case-control studies;African Health Sciences;2022-08-01

2. Hair Dye Ingredients and Potential Health Risks from Exposure to Hair Dyeing;Chemical Research in Toxicology;2022-06-06

3. Risk of Carcinogenicity Associated with Synthetic Hair Dyeing Formulations: A Biochemical View on Action Mechanisms, Genetic Variation and Prevention;Indian Journal of Clinical Biochemistry;2022-05-17

4. Genetic variations in the drug metabolizing enzyme, CYP2E1, among various ethnic populations of Pakistan;PeerJ;2020-08-19

5. Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia;The American Journal of Human Genetics;2020-02

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