Pages that link to "Q59389646"
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The following pages link to Identification of Cytosolic Proteins That Bind to the Fanconi Anemia Complementation Group C Polypeptidein Vitro (Q59389646):
Displaying 11 items.
- Investigation of Fanconi anemia protein interactions by yeast two-hybrid analysis (Q22011168) (← links)
- MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groups (Q24310884) (← links)
- Identification of a novel c-DNA overexpressed in Fanconi's anemia fibroblasts partially homologous to a putative L-3-phosphoserine-phosphatase (Q24313160) (← links)
- Induction of Fanconi anemia cellular phenotype in human 293 cells by overexpression of a mutant FAC allele (Q24562664) (← links)
- Applicability of nonsyngeneic cell models for screening of genes in monogenetics diseases via differential display technique (Q32092439) (← links)
- Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels (Q34390399) (← links)
- Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells (Q37354466) (← links)
- Involvement of the Fanconi anemia protein FA-C in repair processes of oxidative DNA damages. (Q40986622) (← links)
- Development and characterization of immortalized fibroblastoid cell lines from an FA(C) mouse model (Q41022505) (← links)
- New molecular diagnostic tests for two congenital forms of anemia (Q41341822) (← links)
- Is Fanconi anemia caused by a defect in the processing of DNA damage? (Q52184525) (← links)