Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

N G Jaspers

Showing results (51-60 of 71) with videos related to

Pageof 8
Sort By:
Pediatric Research|March 3, 2001
Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancyD I Zafeiriou, F Thorel, A Andreou, et al.
Mutation Research|August 1, 1979
A seventh complementation group in excision-deficient xeroderma pigmentosumW Keijzer, N G Jaspers, P J Abrahams, et al.
American Journal of Human Genetics|June 1, 1992
Ataxia-telangiectasia: linkage evidence for genetic heterogeneityE Sobel, E Lange, N G Jaspers, et al.
Mutation Research|July 1, 1995
Partial characterization of the DNA repair protein complex, containing the ERCC1, ERCC4, ERCC11 and XPF correcting activitiesA J van Vuuren, E Appeldoorn, H Odijk, et al.
Cancer Research|June 11, 1998
Clones of normal keratinocytes and a variety of simultaneously present epidermal neoplastic lesions contain a multitude of p53 gene mutations in a xeroderma pigmentosum patientC Williams, F Pontén, A Ahmadian, et al.
American Journal of Human Genetics|July 10, 2001
Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancyJ M Graham, K Anyane-Yeboa, A Raams, et al.
The Journal of Investigative Dermatology|September 21, 2000
Ultraviolet-B-induced apoptosis and cytokine release in xeroderma pigmentosum keratinocytesC Petit-Frère, E Capulas, J E Lowe, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1994
Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndromeW Vermeulen, A J van Vuuren, M Chipoulet, 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.
Nucleic Acids Research|September 1, 1996
Mutational analysis of the human nucleotide excision repair gene ERCC1A M Sijbers, P J van der Spek, H Odijk, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Pediatric Research|March 3, 2001
Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancyD I Zafeiriou, F Thorel, A Andreou, et al.
Mutation Research|August 1, 1979
A seventh complementation group in excision-deficient xeroderma pigmentosumW Keijzer, N G Jaspers, P J Abrahams, et al.
American Journal of Human Genetics|June 1, 1992
Ataxia-telangiectasia: linkage evidence for genetic heterogeneityE Sobel, E Lange, N G Jaspers, et al.
Mutation Research|July 1, 1995
Partial characterization of the DNA repair protein complex, containing the ERCC1, ERCC4, ERCC11 and XPF correcting activitiesA J van Vuuren, E Appeldoorn, H Odijk, et al.
Cancer Research|June 11, 1998
Clones of normal keratinocytes and a variety of simultaneously present epidermal neoplastic lesions contain a multitude of p53 gene mutations in a xeroderma pigmentosum patientC Williams, F Pontén, A Ahmadian, et al.
American Journal of Human Genetics|July 10, 2001
Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancyJ M Graham, K Anyane-Yeboa, A Raams, et al.
The Journal of Investigative Dermatology|September 21, 2000
Ultraviolet-B-induced apoptosis and cytokine release in xeroderma pigmentosum keratinocytesC Petit-Frère, E Capulas, J E Lowe, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1994
Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndromeW Vermeulen, A J van Vuuren, M Chipoulet, 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.
Nucleic Acids Research|September 1, 1996
Mutational analysis of the human nucleotide excision repair gene ERCC1A M Sijbers, P J van der Spek, H Odijk, et al.
Pageof 8