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Somat Cell Mol Genet ; 22(2): 151-7, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8782494

ABSTRACT

Fanconi anemia (FA) is an autosomal recessive disease characterized by birth defects, progressive bone marrow failure and increased risk for leukemia. FA cells display chromosome breakage and increased cell killing in response to DNA crosslinking agents. At least 5 genes have been defined by cell complementation studies, but only one of these, FAC has been cloned to date. Efforts to map and isolate new FA genes by functional complementation have been hampered by the lack of immortalized FA fibroblast cell lines. Here we report the use of a novel immortalization strategy to create 4 new immortalized FA fibroblast lines, including one from the rare complementation group D.


Subject(s)
Cell Line, Transformed , Fanconi Anemia , Fibroblasts/cytology , Cell Culture Techniques , Cell Fusion , Cell Survival/drug effects , Chromosome Aberrations , Epoxy Compounds/pharmacology , Ethyl Methanesulfonate/pharmacology , Fibroblasts/drug effects , Genetic Complementation Test , Humans , Karyotyping , Mitomycin/pharmacology , Mutagens/pharmacology , Phenotype , Skin/cytology
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