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P A Jeggo

Showing results (51-60 of 72) with videos related to

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Somatic Cell and Molecular Genetics|September 1, 1993
Subchromosomal localization of a gene (XRCC5) involved in double strand break repair to the region 2q34-36M Hafezparast, G P Kaur, M Zdzienicka, et al.
Nucleic Acids Research|March 10, 2000
The C-terminal conserved domain of DNA-PKcs, missing in the SCID mouse, is required for kinase activityH J Beamish, R Jessberger, E Riballo, et al.
Annals of Human Genetics|July 1, 1993
Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21C B Harvey, M F Fox, P A Jeggo, et al.
Journal of Molecular Biology|June 27, 1998
Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joiningM Escarceller, M Buchwald, B K Singleton, et al.
Somatic Cell and Molecular Genetics|January 1, 1993
A hamster-human subchromosomal hybrid cell panel for chromosome 2P A Jeggo, M Hafezparast, A F Thompson, et al.
The EMBO Journal|February 28, 2001
Novel functional requirements for non-homologous DNA end joining in Schizosaccharomyces pombeK G Manolis, E R Nimmo, E Hartsuiker, et al.
The Journal of Biological Chemistry|May 12, 2001
Cellular and biochemical impact of a mutation in DNA ligase IV conferring clinical radiosensitivityE Riballo, A J Doherty, Y Dai, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 1996
Identification of a nonsense mutation in the carboxyl-terminal region of DNA-dependent protein kinase catalytic subunit in the scid mouseT Blunt, D Gell, M Fox, et al.
Molecular and Cellular Biology|March 1, 1997
Molecular and biochemical characterization of xrs mutants defective in Ku80B K Singleton, A Priestley, H Steingrimsdottir, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1992
Localization of a DNA repair gene (XRCC5) involved in double-strand-break rejoining to human chromosome 2P A Jeggo, M Hafezparast, A F Thompson, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
Somatic Cell and Molecular Genetics|September 1, 1993
Subchromosomal localization of a gene (XRCC5) involved in double strand break repair to the region 2q34-36M Hafezparast, G P Kaur, M Zdzienicka, et al.
Nucleic Acids Research|March 10, 2000
The C-terminal conserved domain of DNA-PKcs, missing in the SCID mouse, is required for kinase activityH J Beamish, R Jessberger, E Riballo, et al.
Annals of Human Genetics|July 1, 1993
Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21C B Harvey, M F Fox, P A Jeggo, et al.
Journal of Molecular Biology|June 27, 1998
Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joiningM Escarceller, M Buchwald, B K Singleton, et al.
Somatic Cell and Molecular Genetics|January 1, 1993
A hamster-human subchromosomal hybrid cell panel for chromosome 2P A Jeggo, M Hafezparast, A F Thompson, et al.
The EMBO Journal|February 28, 2001
Novel functional requirements for non-homologous DNA end joining in Schizosaccharomyces pombeK G Manolis, E R Nimmo, E Hartsuiker, et al.
The Journal of Biological Chemistry|May 12, 2001
Cellular and biochemical impact of a mutation in DNA ligase IV conferring clinical radiosensitivityE Riballo, A J Doherty, Y Dai, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 1996
Identification of a nonsense mutation in the carboxyl-terminal region of DNA-dependent protein kinase catalytic subunit in the scid mouseT Blunt, D Gell, M Fox, et al.
Molecular and Cellular Biology|March 1, 1997
Molecular and biochemical characterization of xrs mutants defective in Ku80B K Singleton, A Priestley, H Steingrimsdottir, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1992
Localization of a DNA repair gene (XRCC5) involved in double-strand-break rejoining to human chromosome 2P A Jeggo, M Hafezparast, A F Thompson, et al.
Pageof 8