Smeets D - Search Results

1

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

2

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.

3

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

4

Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

Cerosaletti KM, Lange E, Stringham HM, Weemaes CM, Smeets D, Sölder B, Belohradsky BH, Taylor AM, Karnes P, Elliott A, Komatsu K, Gatti RA, Boehnke M, Concannon P. Cerosaletti KM, et al. Among authors: smeets d. Am J Hum Genet. 1998 Jul;63(1):125-34. doi: 10.1086/301927. Am J Hum Genet. 1998. PMID: 9634525 Free PMC article.

5

The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11.

Komatsu K, Matsuura S, Tauchi H, Endo S, Kodama S, Smeets D, Weemaes C, Oshimura M. Komatsu K, et al. Among authors: smeets d. Am J Hum Genet. 1996 Apr;58(4):885-8. Am J Hum Genet. 1996. PMID: 8644753 Free PMC article. No abstract available.

6

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

7

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.

8

Genetic variation in ICF syndrome: evidence for genetic heterogeneity.

Wijmenga C, Hansen RS, Gimelli G, Björck EJ, Davies EG, Valentine D, Belohradsky BH, van Dongen JJ, Smeets DF, van den Heuvel LP, Luyten JA, Strengman E, Weemaes C, Pearson PL. Wijmenga C, et al. Among authors: smeets df. Hum Mutat. 2000 Dec;16(6):509-17. doi: 10.1002/1098-1004(200012)16:6<509::AID-HUMU8>3.0.CO;2-V. Hum Mutat. 2000. PMID: 11102980 Review.

9

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

10

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.

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