Cargando…
Fanconi anemia complementation group A cells are hypersensitive to chromium(VI)-induced toxicity.
Fanconi anemia (FA) is an autosomal recessive disorder characterized by diverse developmental abnormalities, progressive bone marrow failure, and a markedly increased incidence of malignancy. FA cells are hypersensitive to DNA cross-linking agents, suggesting a general defect in the repair of DNA cr...
Autores principales: | Vilcheck, Susan K, O'Brien, Travis J, Pritchard, Daryl E, Ha, Linan, Ceryak, Susan, Fornsaglio, Jamie L, Patierno, Steven R |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
2002
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241243/ https://www.ncbi.nlm.nih.gov/pubmed/12426130 |
Ejemplares similares
-
Lung Inflammation, Injury, and Proliferative Response after Repetitive Particulate Hexavalent Chromium Exposure
por: Beaver, Laura M., et al.
Publicado: (2009) -
Identification of the Fanconi Anemia Complementation Group I Gene, FANCI
por: Dorsman, Josephine C., et al.
Publicado: (2007) -
Fanconi Anemia complementation group C protein in metabolic disorders
por: Nepal, Manoj, et al.
Publicado: (2018) -
Mutated Fanconi anemia pathway in non-Fanconi anemia cancers
por: Shen, Yihang, et al.
Publicado: (2015) -
Use of the cell division assay to diagnose Fanconi anemia patients' hypersensitivity to mitomycin C
por: Hammarsten, Ola, et al.
Publicado: (2020)