A R Lehmann|S Kirk-Bell - JoVE Visualize

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The British Journal of Dermatology|September 1, 1991

Long-term survival and preservation of natural killer cell activity in a xeroderma pigmentosum patient with spontaneous regression and multiple deposits of malignant melanomaA V Anstey, C F Arlett, J Cole, 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.

Proceedings of the National Academy of Sciences of the United States of America|August 5, 1997

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription geneE M Taylor, B C Broughton, E Botta, et al.

Science (New York, N.Y.)|September 2, 1994

Ku80: product of the XRCC5 gene and its role in DNA repair and V(D)J recombinationG E Taccioli, T M Gottlieb, T Blunt, et al.

Molecular Cell|July 4, 1998

A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophyJ de Boer, J de Wit, H van Steeg, et al.

Gene|June 15, 1988

SV 40-transformed normal and DNA-repair-deficient human fibroblasts can be transfected with high frequency but retain only limited amounts of integrated DNAL V Mayne, T Jones, S W Dean, et al.

The Journal of Investigative Dermatology|October 1, 1996

DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cellsS Moriwaki, M Stefanini, A R Lehmann, et al.

Oncogene|May 12, 2015

USP7 is essential for maintaining Rad18 stability and DNA damage toleranceA Zlatanou, S Sabbioneda, E S Miller, et al.

Mutation Research|January 1, 1992

Workshop on DNA repairA R Lehmann, J H Hoeijmakers, A A van Zeeland, et al.

The British Journal of Radiology|May 23, 2006

Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosumC F Arlett, P N Plowman, P B Rogers, et al.

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Showing results (111-120 of 126) with videos related to

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Pageof 13

The British Journal of Dermatology|September 1, 1991

Long-term survival and preservation of natural killer cell activity in a xeroderma pigmentosum patient with spontaneous regression and multiple deposits of malignant melanomaA V Anstey, C F Arlett, J Cole, 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.

Proceedings of the National Academy of Sciences of the United States of America|August 5, 1997

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription geneE M Taylor, B C Broughton, E Botta, et al.

Science (New York, N.Y.)|September 2, 1994

Ku80: product of the XRCC5 gene and its role in DNA repair and V(D)J recombinationG E Taccioli, T M Gottlieb, T Blunt, et al.

Molecular Cell|July 4, 1998

A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophyJ de Boer, J de Wit, H van Steeg, et al.

Gene|June 15, 1988

SV 40-transformed normal and DNA-repair-deficient human fibroblasts can be transfected with high frequency but retain only limited amounts of integrated DNAL V Mayne, T Jones, S W Dean, et al.

The Journal of Investigative Dermatology|October 1, 1996

DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cellsS Moriwaki, M Stefanini, A R Lehmann, et al.

Oncogene|May 12, 2015

USP7 is essential for maintaining Rad18 stability and DNA damage toleranceA Zlatanou, S Sabbioneda, E S Miller, et al.

Mutation Research|January 1, 1992

Workshop on DNA repairA R Lehmann, J H Hoeijmakers, A A van Zeeland, et al.

The British Journal of Radiology|May 23, 2006

Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosumC F Arlett, P N Plowman, P B Rogers, et al.

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