Zobrazeno 1 - 10 of 166 pro vyhledávání: '"Dirk Bootsma"'
1
Normal chiasma formation in a male with xeroderma pigmentosum
Autor: Maj Hultén, N. E. Skakkebaek., G. Swanbeck, E.A. de Weerd-Kastelein, Dirk Bootsma, A. J. Solari
Publikováno v: Hereditas. 78:117-124
A normal chiasma count was found in first spermatocytes from one patient with the classic symptoms of the genetic disease xeroderma pigmentosum (XP). Skin fibroblasts from this patient and from a brother affected with the same disease demonstrated a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::582423b2b02bb10ea996fccacfa84094
https://doi.org/10.1111/j.1601-5223.1974.tb01434.x
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3
UVB radiation-induced cancer predisposition in Cockayne syndrome group A (Csa) mutant mice
Autor: Jan H.J. Hoeijmakers, Susana Velasco-Miguel, Theo G M F Gorgels, Maaike P.G. Vreeswijk, Errol C. Friedberg, Bep Smit, Dirk Bootsma, Gijsbertus T. J. van der Horst, James A. Richardson, Lisiane B. Meira, Yvonne Kamp, Jan de Wit
Publikováno v: DNA Repair, 1, 143-157. Elsevier
Cockayne syndrome (CS) is an inherited photosensitive neurodevelopmental disorder caused by a specific defect in the transcription-coupled repair (TCR) sub-pathway of NER. Remarkably, despite their DNA repair deficiency, CS patients do not develop sk
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::789b3c1fa5665535bd30a911692611e2
https://pure.eur.nl/en/publications/a3f6bcfb-2b3d-418e-b637-c1049454cf69
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4
The 'Dutch DNA Repair Group', in retrospect
Autor: Dirk Bootsma
Publikováno v: Mutation Research/DNA Repair. 485:37-41
The "Dutch DNA Repair Group" was established about 35 years ago. In this brief historical review some of the crucial decisions are described that have contributed to the relative success of the research of this group. The emphasis of the work of this
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fe632a1eb4d2819a24269b7efe687e3
https://doi.org/10.1016/s0921-8777(00)00080-x
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5
Two Human Homologs of Rad23 Are Functionally Interchangeable in Complex Formation and Stimulation of XPC Repair Activity
Autor: T. Maekawa, A. Aboussekhra, Richard D. Wood, Kaoru Sugasawa, Chikahide Masutani, André P. M. Eker, Fumio Hanaoka, Cécile E. Visser, Jessica M. Y. Ng, A. Uchida, J.H.J. Hoeijmakers, Suzanne Rademakers, Dirk Bootsma, P.J. van der Spek
Publikováno v: Scopus-Elsevier
XPC-hHR23B protein complex is specifically involved in nucleotide excision repair (NER) of DNA lesions on transcriptionally inactive sequences as well as the nontranscribed strand of active genes. Here we demonstrate that not only highly purified rec
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c651a805b57b42a093445b5edefeabe7
https://doi.org/10.1128/mcb.17.12.6924
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6
The Cockayne syndrome B protein, involved in transcription-coupled repair resides in a RNA polymerase II containing complex
Autor: Jean-Marc Egly, Suzanne Rademakers, Wim Vermeulen, Jan H.J. Hoeijmakers, Roselinde I. van Os, Dirk Bootsma, Alain J. van Gool, Elisabetta Citterio, Angelos Constantinou
Publikováno v: EMBO Journal, 16, 5955-5965. Wiley-Blackwell
EMBO Journal
EMBO Journal, 1997, 16 (19), pp.5955-5965. ⟨10.1093/emboj/16.19.5955⟩
International audience; Transcription-coupled repair (TCR), a subpathway of nucleotide excision repair (NER) defective in Cockayne syndrome A and B (CSA and CSB), is responsible for the preferential removal of DNA lesions from the transcribed strand
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f18505392958c005f9263fa00aed59a
https://doi.org/10.1093/emboj/16.19.5955
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7
Discription of mouse RAD54 reduces ionizing radiation resistance and homologous recombination
Autor: Jan H.J. Hoeijmakers, Roland Kanaar, Rudolf W. Hendriks, Christine Troelstra, Jeroen Essers, Sigrid M. A. Swagemakers, Dirk Bootsma, Jan de Wit
Publikováno v: Cell, 89, 195-204. Cell Press
Double-strand DNA break (DSB) repair by homologous recombination occurs through the RAD52 pathway in Saccharomyces cerevisiae. Its biological importance is underscored by the conservation of many RAD52 pathway genes, including RAD54, from fungi to hu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04cccb4e2bcb19c14e3fe0da0549809b
https://pure.eur.nl/en/publications/e0374d25-7a8c-4f45-b3f8-668962af26a0
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8
Cloning, Tissue Expression, and Mapping of a Human Photolyase Homolog with Similarity to Plant Blue-Light Receptors
Autor: P.J. van der Spek, Dirk Bootsma, Masashi Takao, Kumiko Kobayashi, Akira Yasui, André P. M. Eker
Publikováno v: Genomics. 37:177-182
Enzymatic photoreactivation is a DNA repair mechanism that removes UV-induced pyrimidine dimer lesions by action of a single enzyme, photolyase, and visible light. Its presence has been demonstrated in a wide variety of organisms, ranging from simple
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95167f0cb66477e2eefe115443b224ff
https://doi.org/10.1006/geno.1996.0539
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9
XPC and human homologs of RAD23
Autor: Dirk Bootsma, Peter J. van der Spek, Cécile E. Visser, Jan H.J. Hoeijmakers, André P. M. Eker, Chikahide Masutani, Suzanne Rademakers, Kaoru Sugasawa, Fumio Hanaoka
Publikováno v: Nucleic Acids Research, 24(13), 2551-2559. Oxford University Press
The xeroderma pigmentosum syndrome complementation group C (XP-C) is due to a defect in the global genome repair subpathway of nucleotide excision repair (NER). The XPC protein is complexed with HHR23B, one of the two human homologs of the yeast NER
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88fbafc3c578c22c34ca99b4c6d788ec
https://pure.eur.nl/en/publications/838b91f3-beaa-461e-acc8-4a2b59d8e028
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