Importance of finding the bona fide target of the Fanconi anemia pathway
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Fanconi anemia (FA) is a rare genetic disease characterized by the deficiency of the cellular response and repair pathway for DNA interstrand crosslink (ICL) damage. Although recent studies have revealed the detailed molecular functions of FA proteins encoded by 22 genes, the mechanism of occurrence of endogenous ICLs in the human body remains poorly understood. In this short review, we summarize the potential endogenous sources of ICLs counteracted by FA proteins, and provide perspectives on the unanswered questions regarding FA.
収録刊行物
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- Genes and Environment
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Genes and Environment 41 6-6, 2019-03-06
BMC
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詳細情報 詳細情報について
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- CRID
- 1050012570392898560
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- NII論文ID
- 120006619818
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- ISSN
- 18807062
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- HANDLE
- 20.500.14094/90005873
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- IRDB
- Crossref
- CiNii Articles
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