Jaspers NG - Search Results

1

Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2.

Godthelp BC, van Buul PP, Jaspers NG, Elghalbzouri-Maghrani E, van Duijn-Goedhart A, Arwert F, Joenje H, Zdzienicka MZ. Godthelp BC, et al. Among authors: jaspers ng. Mutat Res. 2006 Oct 10;601(1-2):191-201. doi: 10.1016/j.mrfmmm.2006.07.003. Epub 2006 Aug 21. Mutat Res. 2006. PMID: 16920162

2

Immortalization and characterization of Nijmegen Breakage syndrome fibroblasts.

Kraakman-van der Zwet M, Overkamp WJ, Friedl AA, Klein B, Verhaegh GW, Jaspers NG, Midro AT, Eckardt-Schupp F, Lohman PH, Zdzienicka MZ. Kraakman-van der Zwet M, et al. Among authors: jaspers ng. Mutat Res. 1999 May 14;434(1):17-27. doi: 10.1016/s0921-8777(99)00009-9. Mutat Res. 1999. PMID: 10377945

3

Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells.

Kraakman-van der Zwet M, Overkamp WJ, Jaspers NG, Natarajan AT, Lohman PH, Zdzienicka MZ. Kraakman-van der Zwet M, et al. Among authors: jaspers ng. Mutat Res. 2001 Apr 4;485(3):177-85. doi: 10.1016/s0921-8777(00)00078-1. Mutat Res. 2001. PMID: 11267829

4

Brca2 (XRCC11) deficiency results in radioresistant DNA synthesis and a higher frequency of spontaneous deletions.

Kraakman-van der Zwet M, Overkamp WJ, van Lange RE, Essers J, van Duijn-Goedhart A, Wiggers I, Swaminathan S, van Buul PP, Errami A, Tan RT, Jaspers NG, Sharan SK, Kanaar R, Zdzienicka MZ. Kraakman-van der Zwet M, et al. Among authors: jaspers ng. Mol Cell Biol. 2002 Jan;22(2):669-79. doi: 10.1128/MCB.22.2.669-679.2002. Mol Cell Biol. 2002. PMID: 11756561 Free PMC article.

5

Inhibition of DNA synthesis by ionizing radiation: a marker for an S-phase checkpoint.

Jaspers NG, Zdzienicka MZ. Jaspers NG, et al. Methods Mol Biol. 2006;314:51-9. doi: 10.1385/1-59259-973-7:051. Methods Mol Biol. 2006. PMID: 16673873

6

A novel type of X-ray-sensitive Chinese hamster cell mutant with radioresistant DNA synthesis and hampered DNA double-strand break repair.

Verhaegh GW, Jongmans W, Morolli B, Jaspers NG, van der Schans GP, Lohman PH, Zdzienicka MZ. Verhaegh GW, et al. Among authors: jaspers ng. Mutat Res. 1995 Sep;337(2):119-29. doi: 10.1016/0921-8777(95)00017-e. Mutat Res. 1995. PMID: 7565860

7

Co-dominance of radioresistant DNA synthesis in a group of AT-like Chinese hamster cell mutants.

Verhaegh GW, Jaspers NG, Lohman PH, Zdzienicka MZ. Verhaegh GW, et al. Among authors: jaspers ng. Cytogenet Cell Genet. 1993;63(3):176-80. doi: 10.1159/000133528. Cytogenet Cell Genet. 1993. PMID: 8485992

8

The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomes.

Jongmans W, Verhaegh GW, Jaspers NG, Demant P, Natarajan AT, Shiloh Y, Oshimura M, Stanbridge EJ, Athwal RS, Cuthbert AP, Newbold RF, Lohman PH, Zdzienicka MZ. Jongmans W, et al. Among authors: jaspers ng. Mutat Res. 1996 Oct 18;364(2):91-102. doi: 10.1016/0921-8777(96)00027-4. Mutat Res. 1996. PMID: 8879275 Free article.

9

Ataxia-telangiectasia-like Chinese hamster V79 cell mutants with radioresistant DNA synthesis, chromosomal instability, and normal DNA strand break repair.

Zdzienicka MZ, Jaspers NG, van der Schans GP, Natarajan AT, Simons JW. Zdzienicka MZ, et al. Among authors: jaspers ng. Cancer Res. 1989 Mar 15;49(6):1481-5. Cancer Res. 1989. PMID: 2466555

10

A novel radiosensitive SCID patient with a pronounced G(2)/M sensitivity.

Wiegant WW, Meyers M, Verkaik NS, van der Burg M, Darroudi F, Romeijn R, Bernatowska E, Wolska-Kusnierz B, Mikoluc B, Jaspers NG, Vreeken C, Ijspeert H, Esveldt-van Lange RE, Friedl AA, de Villartay JP, Mullenders LH, van Dongen JJ, van Gent DC, Pastink A, Zdzienicka MZ. Wiegant WW, et al. Among authors: jaspers ng. DNA Repair (Amst). 2010 Apr 4;9(4):365-73. doi: 10.1016/j.dnarep.2009.12.004. Epub 2010 Jan 15. DNA Repair (Amst). 2010. PMID: 20079696

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