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D Bootsma

Showing results (101-110 of 165) with videos related to

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Molecular and Cellular Biology|November 1, 1990
Molecular cloning of the human DNA excision repair gene ERCC-6C Troelstra, H Odijk, J de Wit, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|January 30, 1995
Nucleotide excision repair syndromes: molecular basis and clinical symptomsD Bootsma, G Weeda, W Vermeulen, et al.
Nucleic Acids Research|January 25, 1992
Molecular and functional analysis of the XPBC/ERCC-3 promoter: transcription activity is dependent on the integrity of an Sp1-binding siteL Ma, G Weeda, A G Jochemsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1983
Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybridsA H Geurts van Kessel, P A Tetteroo, A E von dem Borne, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1991
Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6M H Koken, P Reynolds, I Jaspers-Dekker, et al.
Cell|August 24, 1990
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndromeG Weeda, R C van Ham, W Vermeulen, et al.
Experimental Cell Research|August 1, 1974
Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridizationH Galjaard, A Hoogeveen, H A de Wit-Verbeek, et al.
Experimental Cell Research|April 1, 1987
Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1W Keijzer, M Stefanini, D Bootsma, et al.
Mutation Research|December 1, 1973
UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotesW J Kleijer, E A de Weerd-Kastelein, M L Sluyter, et al.
Carcinogenesis|December 1, 1991
Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndromeG Weeda, L Ma, R C van Ham, et al.
Pageof 17

Showing results (101-110 of 165) with videos related to

Sort By:
Pageof 17
Molecular and Cellular Biology|November 1, 1990
Molecular cloning of the human DNA excision repair gene ERCC-6C Troelstra, H Odijk, J de Wit, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|January 30, 1995
Nucleotide excision repair syndromes: molecular basis and clinical symptomsD Bootsma, G Weeda, W Vermeulen, et al.
Nucleic Acids Research|January 25, 1992
Molecular and functional analysis of the XPBC/ERCC-3 promoter: transcription activity is dependent on the integrity of an Sp1-binding siteL Ma, G Weeda, A G Jochemsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1983
Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybridsA H Geurts van Kessel, P A Tetteroo, A E von dem Borne, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1991
Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6M H Koken, P Reynolds, I Jaspers-Dekker, et al.
Cell|August 24, 1990
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndromeG Weeda, R C van Ham, W Vermeulen, et al.
Experimental Cell Research|August 1, 1974
Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridizationH Galjaard, A Hoogeveen, H A de Wit-Verbeek, et al.
Experimental Cell Research|April 1, 1987
Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1W Keijzer, M Stefanini, D Bootsma, et al.
Mutation Research|December 1, 1973
UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotesW J Kleijer, E A de Weerd-Kastelein, M L Sluyter, et al.
Carcinogenesis|December 1, 1991
Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndromeG Weeda, L Ma, R C van Ham, et al.
Pageof 17