Huang, Shurong, Lee, Lin, Hanson, Nancy B., Lenaerts, Catherine, Hoehn, Holger, Poot, Martin, ...
The International Registry of Werner syndrome ( www.wernersyndrome.org ) has been providing molecular diagnosis of the Werner syndrome (WS) for the past decade. The present communication summarizes,...
Thesis (Ph. D.)--University of Houston, 1994.
Characterization of the human and mouse WRN 3′→5′ exonuclease
Huang, Shurong, Beresten, Sergey, Li, Baomin, Oshima, Junko, Ellis, Nathan A., Campisi, Judith
Werner’s syndrome (WS) is an autosomal recessive disorder in humans characterized by the premature development of a partial array of age-associated pathologies. WRN, the gene defective in WS,...
Cheng, Wen-Hsing, Kusumoto, Rika, Opresko, Patricia L., Sui, XiuFen, Huang, Shurong, Nicolette, Matthew L., ...
Cells deficient in the Werner syndrome protein (WRN) or BRCA1 are hypersensitive to DNA interstrand cross-links (ICLs), whose repair requires nucleotide excision repair (NER) and homologous...
Characterization of the human and mouse WRN 3′→5′ exonuclease
Huang, Shurong, Beresten, Sergey, Li, Baomin, Oshima, Junko, Ellis, Nathan A., Campisi, Judith
Werner’s syndrome (WS) is an autosomal recessive disorder in humans characterized by the premature development of a partial array of age-associated pathologies. WRN, the gene defective in WS,...
Cheng, Wen-Hsing, Kusumoto, Rika, Opresko, Patricia L., Sui, XiuFen, Huang, Shurong, Nicolette, Matthew L., ...
Cells deficient in the Werner syndrome protein (WRN) or BRCA1 are hypersensitive to DNA interstrand cross-links (ICLs), whose repair requires nucleotide excision repair (NER) and homologous...