Claes KBM - Search Results

1

Chromosomal radiosensitivity of triple negative breast cancer patients.

Francies FZ, Herd O, Cairns A, Nietz S, Murdoch M, Slabbert J, Claes KBM, Vral A, Baeyens A. Francies FZ, et al. Among authors: claes kbm. Int J Radiat Biol. 2019 Nov;95(11):1507-1516. doi: 10.1080/09553002.2019.1649502. Epub 2019 Aug 12. Int J Radiat Biol. 2019. PMID: 31348739

2

Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predisposition.

Baeyens A, Thierens H, Claes K, Poppe B, Messiaen L, De Ridder L, Vral A. Baeyens A, et al. Br J Cancer. 2002 Dec 2;87(12):1379-85. doi: 10.1038/sj.bjc.6600628. Br J Cancer. 2002. PMID: 12454765 Free PMC article.

3

Chromosomal radiosensitivity in BRCA1 and BRCA2 mutation carriers.

Baeyens A, Thierens H, Claes K, Poppe B, de Ridder L, Vral A. Baeyens A, et al. Int J Radiat Biol. 2004 Oct;80(10):745-56. doi: 10.1080/09553000400017937. Int J Radiat Biol. 2004. PMID: 15799620

4

Polymorphisms in nonhomologous end-joining genes associated with breast cancer risk and chromosomal radiosensitivity.

Willems P, Claes K, Baeyens A, Vandersickel V, Werbrouck J, De Ruyck K, Poppe B, Van den Broecke R, Makar A, Marras E, Perletti G, Thierens H, Vral A. Willems P, et al. Genes Chromosomes Cancer. 2008 Feb;47(2):137-48. doi: 10.1002/gcc.20515. Genes Chromosomes Cancer. 2008. PMID: 18000863

5

Acute normal tissue reactions in head-and-neck cancer patients treated with IMRT: influence of dose and association with genetic polymorphisms in DNA DSB repair genes.

Werbrouck J, De Ruyck K, Duprez F, Veldeman L, Claes K, Van Eijkeren M, Boterberg T, Willems P, Vral A, De Neve W, Thierens H. Werbrouck J, et al. Int J Radiat Oncol Biol Phys. 2009 Mar 15;73(4):1187-95. doi: 10.1016/j.ijrobp.2008.08.073. Int J Radiat Oncol Biol Phys. 2009. PMID: 19251090

6

Combined effect of polymorphisms in Rad51 and Xrcc3 on breast cancer risk and chromosomal radiosensitivity.

Vral A, Willems P, Claes K, Poppe B, Perletti G, Thierens H. Vral A, et al. Mol Med Rep. 2011 Sep-Oct;4(5):901-12. doi: 10.3892/mmr.2011.523. Epub 2011 Jul 1. Mol Med Rep. 2011. PMID: 21725594

7

Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives.

Claes K, Depuydt J, Taylor AM, Last JI, Baert A, Schietecatte P, Vandersickel V, Poppe B, De Leeneer K, D'Hooghe M, Vral A. Claes K, et al. Neuromolecular Med. 2013 Sep;15(3):447-57. doi: 10.1007/s12017-013-8231-4. Epub 2013 Apr 30. Neuromolecular Med. 2013. PMID: 23632773

8

Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei.

Francies FZ, Wainwright R, Poole J, De Leeneer K, Coene I, Wieme G, Poirel HA, Brichard B, Vermeulen S, Vral A, Slabbert J, Claes K, Baeyens A. Francies FZ, et al. DNA Repair (Amst). 2018 Jan;61:17-24. doi: 10.1016/j.dnarep.2017.11.001. Epub 2017 Nov 8. DNA Repair (Amst). 2018. PMID: 29154021

9

Accurate quantification of homologous recombination in zebrafish: brca2 deficiency as a paradigm.

Vierstraete J, Willaert A, Vermassen P, Coucke PJ, Vral A, Claes KBM. Vierstraete J, et al. Among authors: claes kbm. Sci Rep. 2017 Nov 28;7(1):16518. doi: 10.1038/s41598-017-16725-3. Sci Rep. 2017. PMID: 29184099 Free PMC article.

10

Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11.

Baert A, Machackova E, Coene I, Cremin C, Turner K, Portigal-Todd C, Asrat MJ, Nuk J, Mindlin A, Young S, MacMillan A, Van Maerken T, Trbusek M, McKinnon W, Wood ME, Foulkes WD, Santamariña M, de la Hoya M, Foretova L, Poppe B, Vral A, Rosseel T, De Leeneer K, Vega A, Claes KBM. Baert A, et al. Among authors: claes kbm. Hum Mutat. 2018 Apr;39(4):515-526. doi: 10.1002/humu.23390. Epub 2018 Jan 22. Hum Mutat. 2018. PMID: 29280214

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