Te Riele HP - Search Results

1

SPO11-independent DNA repair foci and their role in meiotic silencing.

Carofiglio F, Inagaki A, de Vries S, Wassenaar E, Schoenmakers S, Vermeulen C, van Cappellen WA, Sleddens-Linkels E, Grootegoed JA, Te Riele HP, de Massy B, Baarends WM. Carofiglio F, et al. Among authors: te riele hp. PLoS Genet. 2013 Jun;9(6):e1003538. doi: 10.1371/journal.pgen.1003538. Epub 2013 Jun 6. PLoS Genet. 2013. PMID: 23754961 Free PMC article.

2

Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis.

de Vries SS, Baart EB, Dekker M, Siezen A, de Rooij DG, de Boer P, te Riele H. de Vries SS, et al. Genes Dev. 1999 Mar 1;13(5):523-31. doi: 10.1101/gad.13.5.523. Genes Dev. 1999. PMID: 10072381 Free PMC article.

3

Generation of a mouse mutant by oligonucleotide-mediated gene modification in ES cells.

Aarts M, Dekker M, de Vries S, van der Wal A, te Riele H. Aarts M, et al. Nucleic Acids Res. 2006;34(21):e147. doi: 10.1093/nar/gkl896. Epub 2006 Nov 16. Nucleic Acids Res. 2006. PMID: 17142234 Free PMC article.

4

Transient suppression of MLH1 allows effective single-nucleotide substitution by single-stranded DNA oligonucleotides.

Dekker M, de Vries S, Aarts M, Dekker R, Brouwers C, Wiebenga O, de Wind N, Cantelli E, Tonelli R, Te Riele H. Dekker M, et al. Mutat Res. 2011 Oct 1;715(1-2):52-60. doi: 10.1016/j.mrfmmm.2011.07.008. Epub 2011 Jul 27. Mutat Res. 2011. PMID: 21801734

5

RB family tumor suppressor activity may not relate to active silencing of E2F target genes.

Vormer TL, Wojciechowicz K, Dekker M, de Vries S, van der Wal A, Delzenne-Goette E, Naik SH, Song JY, Dannenberg JH, Hansen JB, Te Riele H. Vormer TL, et al. Cancer Res. 2014 Sep 15;74(18):5266-76. doi: 10.1158/0008-5472.CAN-13-3706. Epub 2014 Jul 23. Cancer Res. 2014. PMID: 25056122

6

Temozolomide increases the number of mismatch repair-deficient intestinal crypts and accelerates tumorigenesis in a mouse model of Lynch syndrome.

Wojciechowicz K, Cantelli E, Van Gerwen B, Plug M, Van Der Wal A, Delzenne-Goette E, Song JY, De Vries S, Dekker M, Te Riele H. Wojciechowicz K, et al. Gastroenterology. 2014 Nov;147(5):1064-72.e5. doi: 10.1053/j.gastro.2014.07.052. Epub 2014 Jul 31. Gastroenterology. 2014. PMID: 25088490

7

Effective oligonucleotide-mediated gene disruption in ES cells lacking the mismatch repair protein MSH3.

Dekker M, Brouwers C, Aarts M, van der Torre J, de Vries S, van de Vrugt H, te Riele H. Dekker M, et al. Gene Ther. 2006 Apr;13(8):686-94. doi: 10.1038/sj.gt.3302689. Gene Ther. 2006. PMID: 16437133

8

Fancf-deficient mice are prone to develop ovarian tumours.

Bakker ST, van de Vrugt HJ, Visser JA, Delzenne-Goette E, van der Wal A, Berns MA, van de Ven M, Oostra AB, de Vries S, Kramer P, Arwert F, van der Valk M, de Winter JP, te Riele H. Bakker ST, et al. J Pathol. 2012 Jan;226(1):28-39. doi: 10.1002/path.2992. Epub 2011 Nov 14. J Pathol. 2012. PMID: 21915857

9

LNA modification of single-stranded DNA oligonucleotides allows subtle gene modification in mismatch-repair-proficient cells.

van Ravesteyn TW, Dekker M, Fish A, Sixma TK, Wolters A, Dekker RJ, Te Riele HP. van Ravesteyn TW, et al. Among authors: te riele hp. Proc Natl Acad Sci U S A. 2016 Apr 12;113(15):4122-7. doi: 10.1073/pnas.1513315113. Epub 2016 Mar 7. Proc Natl Acad Sci U S A. 2016. PMID: 26951689 Free PMC article.

10

Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.

Houlleberghs H, Goverde A, Lusseveld J, Dekker M, Bruno MJ, Menko FH, Mensenkamp AR, Spaander MCW, Wagner A, Hofstra RMW, Te Riele H. Houlleberghs H, et al. PLoS Genet. 2017 May 22;13(5):e1006765. doi: 10.1371/journal.pgen.1006765. eCollection 2017 May. PLoS Genet. 2017. PMID: 28531214 Free PMC article.

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