B C Broughton - JoVE Visualize

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Nucleic Acids Research|September 25, 1993

Cloning the RAD51 homologue of Schizosaccharomyces pombeD F Muris, K Vreeken, A M Carr, et al.

American Journal of Human Genetics|February 1, 1996

Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophyK Takayama, E P Salazar, B C Broughton, et al.

Molecular & General Genetics : MGG|September 1, 1991

Assignment of ten DNA repair genes from Schizosaccharomyces pombe to chromosomal NotI restriction fragmentsB C Broughton, N Barbet, J Murray, et al.

Carcinogenesis|January 1, 1983

A biochemical defect in the repair of alkylated DNA in cells from an immunodeficient patient (46BR)I A Teo, B C Broughton, R S Day, 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.

Cancer Research|November 15, 1988

Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndromeA R Lehmann, A E Willis, B C Broughton, et al.

Genomics|August 25, 1999

Novel human and mouse homologs of Saccharomyces cerevisiae DNA polymerase etaJ P McDonald, V Rapić-Otrin, J A Epstein, et al.

Cancer Research|November 1, 1988

Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet lightA R Lehmann, C F Arlett, B C Broughton, et al.

Mutation Research|January 1, 1990

Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: studies using cells from patients with trichothiodystrophyB C Broughton, A R Lehmann, S A Harcourt, et al.

American Journal of Human Genetics|January 1, 1995

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndromeB C Broughton, A F Thompson, S A Harcourt, et al.

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Showing results (11-20 of 24) with videos related to

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Pageof 3

Nucleic Acids Research|September 25, 1993

Cloning the RAD51 homologue of Schizosaccharomyces pombeD F Muris, K Vreeken, A M Carr, et al.

American Journal of Human Genetics|February 1, 1996

Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophyK Takayama, E P Salazar, B C Broughton, et al.

Molecular & General Genetics : MGG|September 1, 1991

Assignment of ten DNA repair genes from Schizosaccharomyces pombe to chromosomal NotI restriction fragmentsB C Broughton, N Barbet, J Murray, et al.

Carcinogenesis|January 1, 1983

A biochemical defect in the repair of alkylated DNA in cells from an immunodeficient patient (46BR)I A Teo, B C Broughton, R S Day, 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.

Cancer Research|November 15, 1988

Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndromeA R Lehmann, A E Willis, B C Broughton, et al.

Genomics|August 25, 1999

Novel human and mouse homologs of Saccharomyces cerevisiae DNA polymerase etaJ P McDonald, V Rapić-Otrin, J A Epstein, et al.

Cancer Research|November 1, 1988

Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet lightA R Lehmann, C F Arlett, B C Broughton, et al.

Mutation Research|January 1, 1990

Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: studies using cells from patients with trichothiodystrophyB C Broughton, A R Lehmann, S A Harcourt, et al.

American Journal of Human Genetics|January 1, 1995

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndromeB C Broughton, A F Thompson, S A Harcourt, et al.

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