Zobrazeno 1 - 10
of 270
pro vyhledávání: '"G Weeda"'
Autor:
Li, Xian1 (AUTHOR) xxt0313@126.com, Li, Danyang1 (AUTHOR), Tian, Ying1 (AUTHOR), Chang, Yaqing1 (AUTHOR) yaqingchang@hotmail.com, Hao, Zhenlin1 (AUTHOR) yaqingchang@hotmail.com
Publikováno v:
Fishes (MDPI AG). Oct2024, Vol. 9 Issue 10, p389. 26p.
Publikováno v:
Medical Education, 31(2), 138-143. Wiley
During their first training period in general practice the authors felt that they did not encounter the balanced workload which is the foundation for learning to be a GP. Previous studies confirmed the existence of differences in overall and specific
Autor:
D. Bootsma, Aart G. Jochemsen, A. Bosch, Libin Ma, G. Weeda, A. Westbroek, A. J. Van Der Eb, J. H. J. Hoeijmakers
Publikováno v:
Molecular and Cellular Biology. 14:4126-4134
The human ERCC3 gene, which corrects specifically the nucleotide excision repair defect in human xeroderma pigmentosum group B and cross-complements the repair deficiency in rodent UV-sensitive mutants of group 3, encodes a presumed DNA helicase that
Publikováno v:
Nucleic Acids Research. 19:6301-6308
The human XPBC/ERCC-3 was cloned by virtue of its ability to correct the excision repair defect of UV-sensitive rodent mutants of complementation group 3. The gene appeared to be in addition implicated in the human, cancer prone repair disorder xerod
Publikováno v:
Carcinogenesis. 12:2361-2368
The human XPBC/ERCC-3 DNA repair gene specifically corrects the repair defect of xeroderma pigmentosum (XP) complementation group B and rodent repair mutant cell lines of group 3. The gene encodes a presumed DNA- and chromatin-binding helicase involv
Autor:
H. Odijk, A. J. Van Der Eb, G. Weeda, D. Bootsma, J. H. J. Hoeijmakers, Andries Westerveld, R. Masurel, J. de Wit, R. C. A. Van Ham
Publikováno v:
Molecular and Cellular Biology. 10:2570-2581
In this report we present the cloning, partial characterization, and preliminary studies of the biological activity of a human gene, designated ERCC-3, involved in early steps of the nucleotide excision repair pathway. The gene was cloned after genom
Autor:
J, de Boer, H, van Steeg, R J, Berg, J, Garssen, J, de Wit, C T, van Oostrum, R B, Beems, G T, van der Horst, C F, van Kreijl, F R, de Gruijl, D, Bootsma, J H, Hoeijmakers, G, Weeda
Publikováno v:
Cancer research. 59(14)
Patients with the nucleotide excision repair (NER) disorder xeroderma pigmentosum (XP) are highly predisposed to develop sunlight-induced skin cancer, in remarkable contrast to photosensitive NER-deficient trichothiodystrophy (TTD) patients carrying
Autor:
G, Weeda, J, de Boer, I, Donker, J, de Wit, S B, Winkler, G T, van der Horst, W, Vermeulen, D, Bootsma, J H, Hoeijmakers
Publikováno v:
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer. 154
Publikováno v:
Environmental and molecular mutagenesis. 31(1)
To study the influence of nucleotide excision repair (NER) on mutagenesis in vivo, ERCC1 +/-, XPA-/-, and wild-type (ERCC1+/+ and XPA+/+, respectively) lambda lacZ-transgenic mice were treated i.p. with N-hydroxy-2-acetylaminofluorene (N-OH-AAF) and
Autor:
G, Weeda, J H, Hoeijmakers
Publikováno v:
Seminars in cancer biology. 4(2)
Nucleotide excision repair is a versatile process and is one of the best known systems that prevents the deleterious consequences of DNA damage induced by environmental agents and cellular metabolites. Without repair, persisting lesions can interfere