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dc.contributor.authorPanahi, Y
dc.contributor.authorFattahi, A
dc.contributor.authorNejabati, HR
dc.contributor.authorAbroon, S
dc.contributor.authorLatifi, Z
dc.contributor.authorAkbarzadeh, A
dc.contributor.authorGhasemnejad, T
dc.date.accessioned2018-08-26T07:12:05Z
dc.date.available2018-08-26T07:12:05Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44584
dc.description.abstractSulfur mustard (SM) is an alkylating agent that causes severe damages to the skin, eyes, and the respiratory system. DNA alkylation is one of the most critical lesions that could lead to monoadducts and cross-links, as well as DNA strand breaks. In response to these adducts, cells initiate a series of reactions to recruit specific DNA repair pathways. The main DNA repair pathways in human cells, which could be involved in the DNA SM-induced DNA damages, are base excision repair (BER), nucleotide excision repair (NER), homologous recombination (HR) and non-homologous end joining (NHEJ). There is, thus, a need for a short review to clarify which damage caused by SM is repaired by which repair pathway. Increasing our knowledge about different DNA repair mechanisms following SM exposure would lay the first step for developing new therapeutic agents to treat people exposed to SM. In this review, we describe the major DNA repair pathways, according to the DNA adducts that can be caused by SM.
dc.language.isoEnglish
dc.relation.ispartofENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY
dc.subjectSulfur mustard
dc.subjectDNA damage
dc.subjectDNA repair
dc.titleDNA repair mechanisms in response to genotoxicity of warfare agent sulfur mustard
dc.typeReview
dc.citation.volume58
dc.citation.spage230
dc.citation.epage236
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.etap.2018.01.012


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