Smeets D - Search Results

1

Hypersensitivity to radiation-induced non-apoptotic and apoptotic death in cell lines from patients with the ICF chromosome instability syndrome.

Narayan A, Tuck-Muller C, Weissbecker K, Smeets D, Ehrlich M. Narayan A, et al. Among authors: smeets d. Mutat Res. 2000 Nov 30;456(1-2):1-15. doi: 10.1016/s0027-5107(00)00103-2. Mutat Res. 2000. PMID: 11087891

2

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

3

DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.

Tuck-Muller CM, Narayan A, Tsien F, Smeets DF, Sawyer J, Fiala ES, Sohn OS, Ehrlich M. Tuck-Muller CM, et al. Among authors: smeets df. Cytogenet Cell Genet. 2000;89(1-2):121-8. doi: 10.1159/000015590. Cytogenet Cell Genet. 2000. PMID: 10894953

4

Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells.

Gisselsson D, Shao C, Tuck-Muller CM, Sogorovic S, Pålsson E, Smeets D, Ehrlich M. Gisselsson D, et al. Among authors: smeets d. Chromosoma. 2005 Jul;114(2):118-26. doi: 10.1007/s00412-005-0343-7. Epub 2005 Apr 27. Chromosoma. 2005. PMID: 15856360

5

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.

6

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.

7

ICF syndrome: high variability of the chromosomal phenotype and association with classical Hodgkin lymphoma.

Schuetz C, Barbi G, Barth TF, Hoenig M, Schulz A, Möeller P, Smeets D, de Greef JC, van der Maarel SM, Vogel W, Debatin KM, Friedrich W. Schuetz C, et al. Among authors: smeets d. Am J Med Genet A. 2007 Sep 1;143A(17):2052-7. doi: 10.1002/ajmg.a.31885. Am J Med Genet A. 2007. PMID: 17702009

8

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.

9

ICF syndrome: a new case and review of the literature.

Smeets DF, Moog U, Weemaes CM, Vaes-Peeters G, Merkx GF, Niehof JP, Hamers G. Smeets DF, et al. Hum Genet. 1994 Sep;94(3):240-6. doi: 10.1007/BF00208277. Hum Genet. 1994. PMID: 8076938 Review.

10

Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in Israel.

Gilad S, Khosravi R, Harnik R, Ziv Y, Shkedy D, Galanty Y, Frydman M, Levi J, Sanal O, Chessa L, Smeets D, Shiloh Y, Bar-Shira A. Gilad S, et al. Among authors: smeets d. Hum Mutat. 1998;11(1):69-75. doi: 10.1002/(SICI)1098-1004(1998)11:1<69::AID-HUMU11>3.0.CO;2-X. Hum Mutat. 1998. PMID: 9450906

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