P G Debenham - JoVE Visualize

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Biochemistry|April 15, 1980

Functional heterogeneity of Escherichia coli ribonucleic acid polymerase holoenzymeA A Travers, R Buckland, P G Debenham

Mutation Research|May 1, 1988

Vector-mediated DNA double-strand break repair analysis in normal, and radiation-sensitive, Chinese hamster V79 cellsP G Debenham, N J Jones, M B Webb

Mutation Research|March 1, 1989

A role of DNA topoisomerases in the active dissociation of DNA minor groove-ligand complexes. A flow cytometric study of inhibitor effectsP J Smith, P G Debenham, J V Watson

Mutation Research|May 1, 1988

Examination of vectors with two dominant, selectable genes for DNA repair and mutation studies in mammalian cellsP G Debenham, M B Webb, A Stretch, et al.

Mutation Research|September 1, 1983

The use of a cloned bacterial gene to study mutation in mammalian cellsJ Thacker, P G Debenham, A Stretch, et al.

International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine|May 1, 1984

DNA-mediated gene transfer into human diploid fibroblasts derived from normal and ataxia-telangiectasia donors: parameters for DNA transfer and properties of DNA transformantsP G Debenham, M B Webb, W K Masson, et al.

Journal of Cell Science. Supplement|January 1, 1987

Molecular studies on the nature of the repair defect in ataxia-telangiectasia and their implications for cellular radiobiologyP G Debenham, M B Webb, N J Jones, et al.

Carcinogenesis|March 1, 1988

A mammalian cell mutant with enhanced capacity to dissociate a bis-benzimidazole dye-DNA complexP J Smith, M Lacy, P G Debenham, et al.

The British Journal of Cancer. Supplement|January 1, 1984

The use of recombinant DNA plasmids for the determination of DNA-repair and recombination in cultured mammalian cellsR Cox, W K Masson, P G Debenham, et al.

Molecular Biology & Medicine|June 1, 1986

Ataxia-telangiectasia: a human mutation giving high-frequency misrepair of DNA double-stranded scissionsR Cox, P G Debenham, W K Masson, et al.

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Showing results (11-20 of 26) with videos related to

Sort By:

Pageof 3

Biochemistry|April 15, 1980

Functional heterogeneity of Escherichia coli ribonucleic acid polymerase holoenzymeA A Travers, R Buckland, P G Debenham

Mutation Research|May 1, 1988

Vector-mediated DNA double-strand break repair analysis in normal, and radiation-sensitive, Chinese hamster V79 cellsP G Debenham, N J Jones, M B Webb

Mutation Research|March 1, 1989

A role of DNA topoisomerases in the active dissociation of DNA minor groove-ligand complexes. A flow cytometric study of inhibitor effectsP J Smith, P G Debenham, J V Watson

Mutation Research|May 1, 1988

Examination of vectors with two dominant, selectable genes for DNA repair and mutation studies in mammalian cellsP G Debenham, M B Webb, A Stretch, et al.

Mutation Research|September 1, 1983

The use of a cloned bacterial gene to study mutation in mammalian cellsJ Thacker, P G Debenham, A Stretch, et al.

International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine|May 1, 1984

DNA-mediated gene transfer into human diploid fibroblasts derived from normal and ataxia-telangiectasia donors: parameters for DNA transfer and properties of DNA transformantsP G Debenham, M B Webb, W K Masson, et al.

Journal of Cell Science. Supplement|January 1, 1987

Molecular studies on the nature of the repair defect in ataxia-telangiectasia and their implications for cellular radiobiologyP G Debenham, M B Webb, N J Jones, et al.

Carcinogenesis|March 1, 1988

A mammalian cell mutant with enhanced capacity to dissociate a bis-benzimidazole dye-DNA complexP J Smith, M Lacy, P G Debenham, et al.

The British Journal of Cancer. Supplement|January 1, 1984

The use of recombinant DNA plasmids for the determination of DNA-repair and recombination in cultured mammalian cellsR Cox, W K Masson, P G Debenham, et al.

Molecular Biology & Medicine|June 1, 1986

Ataxia-telangiectasia: a human mutation giving high-frequency misrepair of DNA double-stranded scissionsR Cox, P G Debenham, W K Masson, et al.

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