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N G Jaspers

Showing results (61-70 of 71) with videos related to

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Cancer Genetics and Cytogenetics|January 1, 1987
Sister chromatid exchanges, hyperdiploidy and chromosomal rearrangements studied in cells from melanoma-prone individuals belonging to families with the dysplastic nevus syndromeN G Jaspers, E J Roza-de Jongh, I G Donselaar, et al.
The EMBO Journal|April 1, 1994
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)A J van Vuuren, W Vermeulen, L Ma, et al.
Cell|December 28, 1999
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorderG S Stewart, R S Maser, T Stankovic, et al.
Human Genetics|March 1, 1992
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndromeY Ziv, M Frydman, E Lange, et al.
Mutation Research|June 23, 1999
Immortalization and characterization of Nijmegen Breakage syndrome fibroblastsM Kraakman-van der Zwet, W J Overkamp, A A Friedl, et al.
Mutation Research|October 18, 1996
The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomesW Jongmans, G W Verhaegh, N G Jaspers, et al.
Mutation Research|June 24, 1998
Impaired DNA repair capacity in skin fibroblasts from various hereditary cancer-prone syndromesP J Abrahams, A Houweling, P D Cornelissen-Steijger, et al.
Cell|September 6, 1996
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonucleaseA M Sijbers, W L de Laat, R R Ariza, et al.
Biochemical Society Transactions|February 1, 1997
Mammalian nucleotide excision repair and syndromesW Vermeulen, J de Boer, E Citterio, et al.
Human Molecular Genetics|April 1, 1996
Predominance of null mutations in ataxia-telangiectasiaS Gilad, R Khosravi, D Shkedy, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Cancer Genetics and Cytogenetics|January 1, 1987
Sister chromatid exchanges, hyperdiploidy and chromosomal rearrangements studied in cells from melanoma-prone individuals belonging to families with the dysplastic nevus syndromeN G Jaspers, E J Roza-de Jongh, I G Donselaar, et al.
The EMBO Journal|April 1, 1994
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)A J van Vuuren, W Vermeulen, L Ma, et al.
Cell|December 28, 1999
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorderG S Stewart, R S Maser, T Stankovic, et al.
Human Genetics|March 1, 1992
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndromeY Ziv, M Frydman, E Lange, et al.
Mutation Research|June 23, 1999
Immortalization and characterization of Nijmegen Breakage syndrome fibroblastsM Kraakman-van der Zwet, W J Overkamp, A A Friedl, et al.
Mutation Research|October 18, 1996
The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomesW Jongmans, G W Verhaegh, N G Jaspers, et al.
Mutation Research|June 24, 1998
Impaired DNA repair capacity in skin fibroblasts from various hereditary cancer-prone syndromesP J Abrahams, A Houweling, P D Cornelissen-Steijger, et al.
Cell|September 6, 1996
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonucleaseA M Sijbers, W L de Laat, R R Ariza, et al.
Biochemical Society Transactions|February 1, 1997
Mammalian nucleotide excision repair and syndromesW Vermeulen, J de Boer, E Citterio, et al.
Human Molecular Genetics|April 1, 1996
Predominance of null mutations in ataxia-telangiectasiaS Gilad, R Khosravi, D Shkedy, et al.
Pageof 8