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N G Jaspers

Showing results (41-50 of 71) with videos related to

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Mutation Research|March 27, 2001
Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cellsM Kraakman-van der Zwet, W J Overkamp, N G Jaspers, et al.
Cancer Research|March 15, 1990
Effects of microinjected photoreactivating enzyme on thymine dimer removal and DNA repair synthesis in normal human and xeroderma pigmentosum fibroblastsL Roza, W Vermeulen, J B Bergen Henegouwen, et al.
Clinical Genetics|September 1, 1979
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repairD J Halley, W Keijzer, N G Jaspers, et al.
Journal of Medical Genetics|July 1, 1996
Xeroderma pigmentosum--Cockayne syndrome complex: a further caseB C Hamel, A Raams, A R Schuitema-Dijkstra, et al.
Human Mutation|October 29, 1998
ATM germline mutations in classical ataxia-telangiectasia patients in the Dutch populationA Broeks, A de Klein, A N Floore, et al.
American Journal of Human Genetics|August 1, 1989
ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndromeC J Curry, P O'Lague, J Tsai, et al.
Mutation Research|September 1, 1995
A novel type of X-ray-sensitive Chinese hamster cell mutant with radioresistant DNA synthesis and hampered DNA double-strand break repairG W Verhaegh, W Jongmans, B Morolli, et al.
Nature|December 8, 1988
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23R A Gatti, I Berkel, E Boder, et al.
Nature Genetics|March 10, 2001
A temperature-sensitive disorder in basal transcription and DNA repair in humansW Vermeulen, S Rademakers, N G Jaspers, et al.
The British Journal of Dermatology|December 15, 2010
Narrowband ultraviolet B inhibits innate cytosolic double-stranded RNA receptors in psoriatic skin and keratinocytesE Rácz, E P Prens, M Kant, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Mutation Research|March 27, 2001
Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cellsM Kraakman-van der Zwet, W J Overkamp, N G Jaspers, et al.
Cancer Research|March 15, 1990
Effects of microinjected photoreactivating enzyme on thymine dimer removal and DNA repair synthesis in normal human and xeroderma pigmentosum fibroblastsL Roza, W Vermeulen, J B Bergen Henegouwen, et al.
Clinical Genetics|September 1, 1979
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repairD J Halley, W Keijzer, N G Jaspers, et al.
Journal of Medical Genetics|July 1, 1996
Xeroderma pigmentosum--Cockayne syndrome complex: a further caseB C Hamel, A Raams, A R Schuitema-Dijkstra, et al.
Human Mutation|October 29, 1998
ATM germline mutations in classical ataxia-telangiectasia patients in the Dutch populationA Broeks, A de Klein, A N Floore, et al.
American Journal of Human Genetics|August 1, 1989
ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndromeC J Curry, P O'Lague, J Tsai, et al.
Mutation Research|September 1, 1995
A novel type of X-ray-sensitive Chinese hamster cell mutant with radioresistant DNA synthesis and hampered DNA double-strand break repairG W Verhaegh, W Jongmans, B Morolli, et al.
Nature|December 8, 1988
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23R A Gatti, I Berkel, E Boder, et al.
Nature Genetics|March 10, 2001
A temperature-sensitive disorder in basal transcription and DNA repair in humansW Vermeulen, S Rademakers, N G Jaspers, et al.
The British Journal of Dermatology|December 15, 2010
Narrowband ultraviolet B inhibits innate cytosolic double-stranded RNA receptors in psoriatic skin and keratinocytesE Rácz, E P Prens, M Kant, et al.
Pageof 8