te Riele H - Search Results

1

Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum.

Wheeler VC, Lebel LA, Vrbanac V, Teed A, te Riele H, MacDonald ME. Wheeler VC, et al. Among authors: te riele h. Hum Mol Genet. 2003 Feb 1;12(3):273-81. doi: 10.1093/hmg/ddg056. Hum Mol Genet. 2003. PMID: 12554681

2

Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.

van den Broek WJ, Nelen MR, Wansink DG, Coerwinkel MM, te Riele H, Groenen PJ, Wieringa B. van den Broek WJ, et al. Among authors: te riele h. Hum Mol Genet. 2002 Jan 15;11(2):191-8. doi: 10.1093/hmg/11.2.191. Hum Mol Genet. 2002. PMID: 11809728

3

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.

Foiry L, Dong L, Savouret C, Hubert L, te Riele H, Junien C, Gourdon G. Foiry L, et al. Among authors: te riele h. Hum Genet. 2006 Jun;119(5):520-6. doi: 10.1007/s00439-006-0164-7. Epub 2006 Mar 22. Hum Genet. 2006. PMID: 16552576

4

Mice defective in the mismatch repair gene Msh2 show increased predisposition to UVB radiation-induced skin cancer.

Meira LB, Cheo DL, Reis AM, Claij N, Burns DK, te Riele H, Friedberg EC. Meira LB, et al. Among authors: te riele h. DNA Repair (Amst). 2002 Nov 3;1(11):929-34. doi: 10.1016/s1568-7864(02)00143-x. DNA Repair (Amst). 2002. PMID: 12531020

5

Characterization of MSH2 variants by endogenous gene modification in mouse embryonic stem cells.

Wielders EA, Dekker RJ, Holt I, Morris GE, te Riele H. Wielders EA, et al. Among authors: te riele h. Hum Mutat. 2011 Apr;32(4):389-96. doi: 10.1002/humu.21448. Epub 2011 Mar 8. Hum Mutat. 2011. PMID: 21309037 Free article.

6

Methylation tolerance in mismatch repair proficient cells with low MSH2 protein level.

Claij N, Te Riele H. Claij N, et al. Among authors: te riele h. Oncogene. 2002 Apr 25;21(18):2873-9. doi: 10.1038/sj.onc.1205395. Oncogene. 2002. PMID: 11973647

7

HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions.

de Wind N, Dekker M, Claij N, Jansen L, van Klink Y, Radman M, Riggins G, van der Valk M, van't Wout K, te Riele H. de Wind N, et al. Among authors: te riele h. Nat Genet. 1999 Nov;23(3):359-62. doi: 10.1038/15544. Nat Genet. 1999. PMID: 10545954

8

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer.

de Wind N, Dekker M, Berns A, Radman M, te Riele H. de Wind N, et al. Among authors: te riele h. Cell. 1995 Jul 28;82(2):321-30. doi: 10.1016/0092-8674(95)90319-4. Cell. 1995. PMID: 7628020 Free article.

9

Functional analysis of MSH2 unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repair.

Wielders EA, Hettinger J, Dekker R, Kets CM, Ligtenberg MJ, Mensenkamp AR, van den Ouweland AM, Prins J, Wagner A, Dinjens WN, Dubbink HJ, van Hest LP, Menko F, Hogervorst F, Verhoef S, te Riele H. Wielders EA, et al. Among authors: te riele h. J Med Genet. 2014 Apr;51(4):245-53. doi: 10.1136/jmedgenet-2013-101987. Epub 2014 Feb 5. J Med Genet. 2014. PMID: 24501230

10

DNA mismatch repair deficiency stimulates N-ethyl-N-nitrosourea-induced mutagenesis and lymphomagenesis.

Claij N, van der Wal A, Dekker M, Jansen L, te Riele H. Claij N, et al. Among authors: te riele h. Cancer Res. 2003 May 1;63(9):2062-6. Cancer Res. 2003. PMID: 12727820

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