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E C Friedberg

Showing results (201-210 of 214) with videos related to

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Cell|December 31, 1993
Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repairW J Feaver, J Q Svejstrup, L Bardwell, et al.
Cold Spring Harbor Symposia on Quantitative Biology|May 23, 2003
Human DNA polymerase kappa: a novel DNA polymerase of unknown biological function encoded by the DINB1 geneV L Gerlach, W J Feaver, P L Fischhaber, et al.
Oncogene|October 24, 2000
Age-dependent spontaneous mutagenesis in Xpc mice defective in nucleotide excision repairS W Wijnhoven, H J Kool, L H Mullenders, et al.
Environmental and Molecular Mutagenesis|August 12, 2005
3,4-Epoxy-1-butene, a reactive metabolite of 1,3-butadiene, induces somatic mutations in Xpc-null miceJ K Wickliffe, L A Galbert, M M Ammenheuser, et al.
American Journal of Human Genetics|March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) geneL B Meira, J M Graham, C R Greenberg, et al.
Basic Life Sciences|January 1, 1986
Molecular approaches to the study of nucleotide excision repair in eukaryotesE C Friedberg, D P Barbis, J M Chenevert, et al.
Mutation Research|September 1, 1987
Molecular aspects of DNA repairE C Friedberg, C Backendorf, J Burke, et al.
The Journal of Investigative Dermatology|November 17, 2001
The DNA damage signal for Mdm2 regulation, Trp53 induction, and sunburn cell formation in vivo originates from actively transcribed genesD E Brash, N M Wikonkal, E Remenyik, et al.
Mutation Research|March 4, 1997
Characterization of defective nucleotide excision repair in XPC mutant miceD L Cheo, H J Ruven, L B Meira, et al.
Cell|August 25, 1995
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIHK A Henning, L Li, N Iyer, et al.
Pageof 22

Showing results (201-210 of 214) with videos related to

Sort By:
Pageof 22
Cell|December 31, 1993
Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repairW J Feaver, J Q Svejstrup, L Bardwell, et al.
Cold Spring Harbor Symposia on Quantitative Biology|May 23, 2003
Human DNA polymerase kappa: a novel DNA polymerase of unknown biological function encoded by the DINB1 geneV L Gerlach, W J Feaver, P L Fischhaber, et al.
Oncogene|October 24, 2000
Age-dependent spontaneous mutagenesis in Xpc mice defective in nucleotide excision repairS W Wijnhoven, H J Kool, L H Mullenders, et al.
Environmental and Molecular Mutagenesis|August 12, 2005
3,4-Epoxy-1-butene, a reactive metabolite of 1,3-butadiene, induces somatic mutations in Xpc-null miceJ K Wickliffe, L A Galbert, M M Ammenheuser, et al.
American Journal of Human Genetics|March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) geneL B Meira, J M Graham, C R Greenberg, et al.
Basic Life Sciences|January 1, 1986
Molecular approaches to the study of nucleotide excision repair in eukaryotesE C Friedberg, D P Barbis, J M Chenevert, et al.
Mutation Research|September 1, 1987
Molecular aspects of DNA repairE C Friedberg, C Backendorf, J Burke, et al.
The Journal of Investigative Dermatology|November 17, 2001
The DNA damage signal for Mdm2 regulation, Trp53 induction, and sunburn cell formation in vivo originates from actively transcribed genesD E Brash, N M Wikonkal, E Remenyik, et al.
Mutation Research|March 4, 1997
Characterization of defective nucleotide excision repair in XPC mutant miceD L Cheo, H J Ruven, L B Meira, et al.
Cell|August 25, 1995
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIHK A Henning, L Li, N Iyer, et al.
Pageof 22