Showing results (11-20 of 253) with videos related to
Sort By:
Pageof 26
Genomics|December 11, 1991
Rat hypoxanthine phosphoribosyltransferase cDNA cloning and sequence analysisT A Chiaverotti, N Battula, R J MonnatProceedings of the National Academy of Sciences of the United States of America|August 1, 1989
Mutator phenotype of Werner syndrome is characterized by extensive deletionsK Fukuchi, G M Martin, R J MonnatHuman Mutation|July 17, 1999
Different somatic and germline HPRT1 mutations promote use of a common, cryptic intron 1 splice site. Mutations in brief no. 246. OnlineL M Colgin, A F Hackmann, R J MonnatNature Structural Biology|March 29, 2001
The homing endonuclease I-CreI uses three metals, one of which is shared between the two active sitesB S Chevalier, R J Monnat, B L StoddardGenomics|July 11, 1992
Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletionsR J Monnat, A F Hackmann, T A ChiaverottiMutation Research|August 1, 1993
Spectrum of spontaneous mutation in animal cells containing an aphidicolin-resistant DNA polymerase alphaP K Liu, J M Trujillo, R J MonnatHuman Mutation|August 14, 1999
Different somatic and germline HPRT1 mutations promote use of a common, cryptic intron 1 splice site. Mutation in brief no. 259. OnlineL M Colgin, A F Hackmann, R J MonnatGenes & Development|April 24, 2001
Loss of Werner syndrome protein function promotes aberrant mitotic recombinationP R Prince, M J Emond, R J MonnatPageof 26