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Cell
|
December 31, 1993
Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair
W 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 gene
V 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 repair
S 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 mice
J 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) gene
L 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 eukaryotes
E C Friedberg, D P Barbis, J M Chenevert, et al.
Mutation Research
|
September 1, 1987
Molecular aspects of DNA repair
E 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 genes
D E Brash, N M Wikonkal, E Remenyik, et al.
Mutation Research
|
March 4, 1997
Characterization of defective nucleotide excision repair in XPC mutant mice
D 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 TFIIH
K A Henning, L Li, N Iyer, et al.
Page
of 22
Search research articles
Search
Showing results (201-210 of 214) with videos related to
Sort By:
Page
of 22
Cell
|
December 31, 1993
Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair
W 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 gene
V 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 repair
S 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 mice
J 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) gene
L 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 eukaryotes
E C Friedberg, D P Barbis, J M Chenevert, et al.
Mutation Research
|
September 1, 1987
Molecular aspects of DNA repair
E 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 genes
D E Brash, N M Wikonkal, E Remenyik, et al.
Mutation Research
|
March 4, 1997
Characterization of defective nucleotide excision repair in XPC mutant mice
D 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 TFIIH
K A Henning, L Li, N Iyer, et al.
Page
of 22