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Results: 1-10 |
Results: 10
A temperature-sensitive disorder in basal transcription and DNA repair in humans
Authors: Vermeulen, W Rademakers, S Jaspers, NGJ Appeldoorn, E Raams, A Klein, B Kleijer, WJ Hansen, LK Hoeijmakers, JHJ
Citation: W. Vermeulen et al., A temperature-sensitive disorder in basal transcription and DNA repair in humans, NAT GENET, 27(3), 2001, pp. 299-303
Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells
Authors: Kraakman-van der Zwet, M Overkamp, WJI Jaspers, NGJ Natarajan, AT Lohman, PHM Zdzienicka, MZ
Citation: M. Kraakman-van Der Zwet et al., Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells, MUT R-DNA R, 485(3), 2001, pp. 177-185
Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy
Authors: Zafeiriou, DI Thorel, F Andreou, A Kleijer, WJ Raams, A Garritsen, VH Gombakis, N Jaspers, NGJ Clarkson, SG
Citation: Di. Zafeiriou et al., Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy, PEDIAT RES, 49(3), 2001, pp. 407-412
A case of Rombo syndrome
Authors: Van Steensel, MAM Jaspers, NGJ Steijlen, PM
Citation: Mam. Van Steensel et al., A case of Rombo syndrome, BR J DERM, 144(6), 2001, pp. 1215-1218
Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy
Authors: Graham, JM Anyane-Yeboa, K Raams, A Appeldoorn, E Kleijer, WJ Garritsen, VH Busch, D Edersheim, TG Jaspers, NGJ
Citation: Jm. Graham et al., Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy, AM J HU GEN, 69(2), 2001, pp. 291-300
Ultraviolet-B-induced apoptosis and cytokine release in xeroderma pigmentosum keratinocytes
Authors: Petit-Frere, C Capulas, E Lowe, JE Koulu, L Marttila, RJ Jaspers, NGJ Clingen, PH Green, MHL Arlett, CF
Citation: C. Petit-frere et al., Ultraviolet-B-induced apoptosis and cytokine release in xeroderma pigmentosum keratinocytes, J INVES DER, 115(4), 2000, pp. 687-693
Immortalization and characterization of Nijmegen Breakage Syndrome fibroblasts
Authors: Kraakman-van der Zwet, M Overkamp, WJI Friedl, AA Klein, B Verhaegh, GWCT Jaspers, NGJ Midro, AT Eckardt-Schupp, F Lohman, PHM Zdzienicka, MZ
Citation: M. Kraakman-van Der Zwet et al., Immortalization and characterization of Nijmegen Breakage Syndrome fibroblasts, MUT R-DNA R, 434(1), 1999, pp. 17-27
Molecular mechanism of nucleotide excision repair
Authors: de Laat, WL Jaspers, NGJ Hoeijmakers, JHJ
Citation: Wl. De Laat et al., Molecular mechanism of nucleotide excision repair, GENE DEV, 13(7), 1999, pp. 768-785
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder
Authors: Stewart, GS Maser, RS Stankovic, T Bressan, DA Kaplan, MI Jaspers, NGJ Raams, A Byrd, PJ Petrini, JHJ Taylor, AMR
Citation: Gs. Stewart et al., The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder, CELL, 99(6), 1999, pp. 577-587
Inhibition of DNA synthesis by ionizing radiation
Authors: Jaspers, NGJ Zdzienicka, MZ
Citation: Ngj. Jaspers et Mz. Zdzienicka, Inhibition of DNA synthesis by ionizing radiation, METH MOL B, 113, 1999, pp. 535-542
Risultati: 1-10 |