The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases

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Trends in Genetics, Vol. 16, Iss. 5, 2000-05 ,pp. : 213-220

Elsevier

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Cloning and characterization of two Arabidopsis genes that belong to the RAD21/REC8 family of chromosome cohesin proteins

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SMARCAD1, a Novel Human Helicase Family-Defining Member Associated with Genetic Instability: Cloning, Expression, and Mapping to 4q22-q23, a Band Rich in Breakpoints and Deletion Mutants Involved in Several Human Diseases

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Genomics, Vol. 69, Iss. 2, 2000-10 ,pp. : 162-173

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Two Novel Mouse Genes-Nubp2, Mapped to the t-Complex on Chromosome 17, and Nubp1, Mapped to Chromosome 16- Establish a New Gene Family of Nucleotide-Binding Proteins in Eukaryotes

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Genomics, Vol. 60, Iss. 2, 1999-09 ,pp. : 152-160

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RecQ helicases and topoisomerase III in cancer and aging

By Laursen L.V.  

Biogerontology, Vol. 4, Iss. 5, 2003-01 ,pp. : 275-287

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