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S G Clarkson

Showing results (31-40 of 42) with videos related to

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Nature|May 13, 1993
Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2D Scherly, T Nouspikel, J Corlet, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG functionT Nouspikel, P Lalle, S A Leadon, et al.
Cell|November 1, 1980
Mutations of the yeast SUP4 tRNATyr locus: transcription of the mutant genes in vitroR A Koski, S G Clarkson, J Kurjan, et al.
Experimental Cell Research|August 26, 1998
Complementation of transformed fibroblasts from patients with combined xeroderma pigmentosum-Cockayne syndromeA R Ellison, T Nouspikel, N G Jaspers, et al.
Nucleic Acids Research|October 1, 1976
Integration of eukaryotic genes for 5S RNA and histone proteins into a phage lambda receptorS G Clarkson, H O Smith, W Schaffner, et al.
The Journal of Biological Chemistry|February 20, 1999
Conserved residues of human XPG protein important for nuclease activity and function in nucleotide excision repairA Constantinou, D Gunz, E Evans, et al.
Genomics|May 1, 1994
The human gene for xeroderma pigmentosum complementation group G (XPG) maps to 13q33 by fluorescence in situ hybridizationS Samec, T A Jones, J Corlet, et al.
Human Molecular Genetics|January 1, 1994
Dinucleotide repeat polymorphism within ERCC5 geneS Samec, S G Clarkson, J Blaschak, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1979
Delimitation of a promoter for RNA polymerase III by means of a functional testJ L Telford, A Kressmann, R A Koski, et al.
Mutation Research|July 1, 1994
Nomenclature of human DNA repair genesA R Lehmann, D Bootsma, S G Clarkson, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Nature|May 13, 1993
Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2D Scherly, T Nouspikel, J Corlet, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG functionT Nouspikel, P Lalle, S A Leadon, et al.
Cell|November 1, 1980
Mutations of the yeast SUP4 tRNATyr locus: transcription of the mutant genes in vitroR A Koski, S G Clarkson, J Kurjan, et al.
Experimental Cell Research|August 26, 1998
Complementation of transformed fibroblasts from patients with combined xeroderma pigmentosum-Cockayne syndromeA R Ellison, T Nouspikel, N G Jaspers, et al.
Nucleic Acids Research|October 1, 1976
Integration of eukaryotic genes for 5S RNA and histone proteins into a phage lambda receptorS G Clarkson, H O Smith, W Schaffner, et al.
The Journal of Biological Chemistry|February 20, 1999
Conserved residues of human XPG protein important for nuclease activity and function in nucleotide excision repairA Constantinou, D Gunz, E Evans, et al.
Genomics|May 1, 1994
The human gene for xeroderma pigmentosum complementation group G (XPG) maps to 13q33 by fluorescence in situ hybridizationS Samec, T A Jones, J Corlet, et al.
Human Molecular Genetics|January 1, 1994
Dinucleotide repeat polymorphism within ERCC5 geneS Samec, S G Clarkson, J Blaschak, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1979
Delimitation of a promoter for RNA polymerase III by means of a functional testJ L Telford, A Kressmann, R A Koski, et al.
Mutation Research|July 1, 1994
Nomenclature of human DNA repair genesA R Lehmann, D Bootsma, S G Clarkson, et al.
Pageof 5