Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Bep Smit"'
Publikováno v:
BJOG, 115(9), 1131-1137. Wiley-Blackwell
OBJECTIVE: The aim of this study was to describe the variation of normal maternal temperature during labour. Design A prospective cohort study. SETTING: Two hospitals in Amsterdam, the Netherlands. POPULATION: All women with a live singleton pregnanc
Autor:
E.A.P. Steegers, Irene A.L. Groenenberg, Anton H. J. Koning, C. Brezinka, P.J. van der Spek, C. M. Verwoerd-Dikkeboom, Bep Smit
Publikováno v:
Ultrasound in Obstetrics & Gynecology, 32(4), 510-514. John Wiley & Sons Ltd.
Objective The utility of a virtual reality system was examined in the visualization of three-dimensional (3D) ultrasound images of fetal ambiguous genitalia. Methods In 2005, fetal ambiguous genitalia were diagnosed in four patients referred to our d
Autor:
Bep Smit, Cecile E.M.T. Beerens, Jeroen Essers, Jan H.J. Hoeijmakers, Joanna Wesoly, Mies L. G. Dronkert, Claire Wyman, Rudi W. Hendriks, Roland Kanaar
Publikováno v:
DNA Repair, 1, 779-793. Elsevier
Homologous recombination is one of the major pathways for repair of DNA double-strand breaks (DSBs). Important proteins in this pathway are Rad51 and Rad54. Rad51 forms a nucleoprotein filament on single-stranded DNA (ssDNA) that mediates pairing wit
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
Autor:
Bep Smit, Peter B. Moens, Jennifer H. Lees, Elaine M. Taylor, Jeelan S. Moghraby, Alan R. Lehmann
Publikováno v:
Molecular Biology of the Cell. 12:1583-1594
The structural maintenance of chromosomes (SMC) protein encoded by the fission yeast rad18 gene is involved in several DNA repair processes and has an essential function in DNA replication and mitotic control. It has a heterodimeric partner SMC prote
Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in mice
Autor:
R. van Os, Manja Muijtjens, Antony M. Carr, J.H.J. Hoeijmakers, Alan R. Lehmann, Bep Smit, A. de Klein, Y. Verhoeven
Publikováno v:
Current Biology, 10(8), 479-482. Cell Press
Checkpoints of DNA integrity are conserved throughout evolution, as are the kinases ATM ( Ataxia Telangiectasia mutated ) and ATR (Ataxia- and Rad-related), which are related to phosphatidylinositol (PI) 3-kinase [1–3]. The ATM gene is not essentia
Autor:
Wolf Dietrich Heyer, Roland Kanaar, Jan Huib Franssen, Albert Pastink, Jeroen Essers, Bep Smit, Jean-Marie Buerstedde, Beate Clever, Sigrid M. A. Swagemakers, Jan H.J. Hoeijmakers, Christine Troelstra, Olga Bezzubova
Publikováno v:
Current Biology. 6:828-838
Background: Homologous recombination is of eminent importance both in germ cells, to generate genetic diversity during meiosis, and in somatic cells, to safeguard DNA from genotoxic damage. The genetically well-defined RAD52 pathway is required for t
Autor:
Elaine M. Taylor, Moghraby, Jeelan S., Lees, Jennifer H., Bep Smit, Moens, Peter B., Lehmann, Alan R.
Publikováno v:
Lancaster University-Pure
The structural maintenance of chromosomes (SMC) protein encoded by the fission yeast rad18 gene is involved in several DNA repair processes and has an essential function in DNA replication and mitotic control. It has a heterodimeric partner SMC prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::139d50434ee170ee422410d1362d8322
https://eprints.lancs.ac.uk/id/eprint/60120/
https://eprints.lancs.ac.uk/id/eprint/60120/
Autor:
Shin Ichiro Kanno, Gijsbertus T. J. van der Horst, Kumiko Kobayashi, Masashi Takao, Bep Smit, Akira Yasui
Publikováno v:
Nucleic Acids Research, 26(22), 5086-5092. Oxford University Press
We isolated and characterized mouse photolyase-like genes, mCRY1 (mPHLL1) and mCRY2 (mPHLL2), which belong to the photolyase family including plant blue-light receptors. The mCRY1 and mCRY2 genes are located on chromosome 10C and 2E, respectively, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba60c0f01eb43bdd4aadb38f685d8a25
https://pure.eur.nl/en/publications/cb5be5df-a093-4e4e-8af5-c797c45251ea
https://pure.eur.nl/en/publications/cb5be5df-a093-4e4e-8af5-c797c45251ea
Autor:
Bep Smit, Michael J. McKay, Roland Kanaar, Dirk Bootsma, Anne Hagemeijer, Peter van der, Jan H.J. Hoeijmakers, Christine Troelstra
Publikováno v:
Genomics. 36(2)
The rad21 gene of Schizosaccharomyces pombe is involved in the repair of ionizing radiation-induced DNA double-strand breaks. The isolation of mouse and human putative homologs of rad21 is reported here. Alignment of the predicted amino acid sequence