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R J Monnat

Showing results (11-20 of 46) with videos related to

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Advances in Experimental Medicine and Biology|January 11, 1991
Rat hypoxanthine phosphoribosyltransferase cDNA cloning and sequence analysisT A Chiaverotti, N Battula, R J Monnat
Human Mutation|April 29, 1999
WRN mutations in Werner syndromeM J Moser, J Oshima, R J Monnat
Genomics|December 11, 1991
Rat hypoxanthine phosphoribosyltransferase cDNA cloning and sequence analysisT A Chiaverotti, N Battula, R J Monnat
Cancer Research|August 15, 1988
Resistance of HeLa cell mitochondrial DNA to mutagenesis by chemical carcinogensS Mita, R J Monnat, L A Loeb
Proceedings 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 Monnat
Human 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 Monnat
Nature 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 Stoddard
Genomics|July 11, 1992
Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletionsR J Monnat, A F Hackmann, T A Chiaverotti
Mutation 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 Monnat
Human 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 Monnat
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Advances in Experimental Medicine and Biology|January 11, 1991
Rat hypoxanthine phosphoribosyltransferase cDNA cloning and sequence analysisT A Chiaverotti, N Battula, R J Monnat
Human Mutation|April 29, 1999
WRN mutations in Werner syndromeM J Moser, J Oshima, R J Monnat
Genomics|December 11, 1991
Rat hypoxanthine phosphoribosyltransferase cDNA cloning and sequence analysisT A Chiaverotti, N Battula, R J Monnat
Cancer Research|August 15, 1988
Resistance of HeLa cell mitochondrial DNA to mutagenesis by chemical carcinogensS Mita, R J Monnat, L A Loeb
Proceedings 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 Monnat
Human 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 Monnat
Nature 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 Stoddard
Genomics|July 11, 1992
Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletionsR J Monnat, A F Hackmann, T A Chiaverotti
Mutation 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 Monnat
Human 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 Monnat
Pageof 5