Smeets D - Search Results

1

Nijmegen breakage syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiation.

Jongmans W, Vuillaume M, Chrzanowska K, Smeets D, Sperling K, Hall J. Jongmans W, et al. Among authors: smeets d. Mol Cell Biol. 1997 Sep;17(9):5016-22. doi: 10.1128/MCB.17.9.5016. Mol Cell Biol. 1997. PMID: 9271379 Free PMC article.

2

Radiation induction of p53 in cells from Nijmegen breakage syndrome is defective but not similar to ataxia-telangiectasia.

Matsuura K, Balmukhanov T, Tauchi H, Weemaes C, Smeets D, Chrzanowska K, Endou S, Matsuura S, Komatsu K. Matsuura K, et al. Among authors: smeets d. Biochem Biophys Res Commun. 1998 Jan 26;242(3):602-7. doi: 10.1006/bbrc.1997.7924. Biochem Biophys Res Commun. 1998. PMID: 9464263

3

Nijmegen breakage syndrome.

van der Burgt I, Chrzanowska KH, Smeets D, Weemaes C. van der Burgt I, et al. Among authors: smeets d. J Med Genet. 1996 Feb;33(2):153-6. doi: 10.1136/jmg.33.2.153. J Med Genet. 1996. PMID: 8929954 Free PMC article. Review.

4

DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes.

Ehrlich M, Buchanan KL, Tsien F, Jiang G, Sun B, Uicker W, Weemaes CM, Smeets D, Sperling K, Belohradsky BH, Tommerup N, Misek DE, Rouillard JM, Kuick R, Hanash SM. Ehrlich M, et al. Among authors: smeets d. Hum Mol Genet. 2001 Dec 1;10(25):2917-31. doi: 10.1093/hmg/10.25.2917. Hum Mol Genet. 2001. PMID: 11741835

5

Variants of Nijmegen breakage syndrome and ataxia telangiectasia.

Weemaes CM, Smeets DF, Horstink M, Haraldsson A, Bakkeren JA. Weemaes CM, et al. Among authors: smeets df. Immunodeficiency. 1993;4(1-4):109-11. Immunodeficiency. 1993. PMID: 7513225

6

Nijmegen Breakage syndrome: a progress report.

Weemaes CM, Smeets DF, van der Burgt CJ. Weemaes CM, et al. Among authors: smeets df. Int J Radiat Biol. 1994 Dec;66(6 Suppl):S185-8. Int J Radiat Biol. 1994. PMID: 7836846 Review.

7

Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24.

Matsuura S, Weemaes C, Smeets D, Takami H, Kondo N, Sakamoto S, Yano N, Nakamura A, Tauchi H, Endo S, Oshimura M, Komatsu K. Matsuura S, et al. Among authors: smeets d. Am J Hum Genet. 1997 Jun;60(6):1487-94. doi: 10.1086/515461. Am J Hum Genet. 1997. PMID: 9199571 Free PMC article.

8

Positional cloning of the gene for Nijmegen breakage syndrome.

Matsuura S, Tauchi H, Nakamura A, Kondo N, Sakamoto S, Endo S, Smeets D, Solder B, Belohradsky BH, Der Kaloustian VM, Oshimura M, Isomura M, Nakamura Y, Komatsu K. Matsuura S, et al. Among authors: smeets d. Nat Genet. 1998 Jun;19(2):179-81. doi: 10.1038/549. Nat Genet. 1998. PMID: 9620777

9

Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalis.

Semmekrot BA, Haraldsson A, Weemaes CM, Smeets DF, Geven WB, Brunner HG. Semmekrot BA, et al. Among authors: smeets df. Am J Med Genet. 1992 Mar 1;42(5):736-40. doi: 10.1002/ajmg.1320420523. Am J Med Genet. 1992. PMID: 1632450

10

Localization of the ICF syndrome to chromosome 20 by homozygosity mapping.

Wijmenga C, van den Heuvel LP, Strengman E, Luyten JA, van der Burgt IJ, de Groot R, Smeets DF, Draaisma JM, van Dongen JJ, De Abreu RA, Pearson PL, Sandkuijl LA, Weemaes CM. Wijmenga C, et al. Among authors: smeets df. Am J Hum Genet. 1998 Sep;63(3):803-9. doi: 10.1086/302021. Am J Hum Genet. 1998. PMID: 9718351 Free PMC article.

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