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Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.
Nat Genet. 2009 Jan;41(1):112-7. doi: 10.1038/ng.283. Epub 2008 Dec 21.
Nat Genet. 2009.
PMID: 19098912
Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors.
Mensenkamp AR, Vogelaar IP, van Zelst-Stams WA, Goossens M, Ouchene H, Hendriks-Cornelissen SJ, Kwint MP, Hoogerbrugge N, Nagtegaal ID, Ligtenberg MJ.
Mensenkamp AR, et al. Among authors: hendriks cornelissen sj.
Gastroenterology. 2014 Mar;146(3):643-646.e8. doi: 10.1053/j.gastro.2013.12.002. Epub 2013 Dec 10.
Gastroenterology. 2014.
PMID: 24333619
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Reliable Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue Using Single Molecule Tags.
Eijkelenboom A, Kamping EJ, Kastner-van Raaij AW, Hendriks-Cornelissen SJ, Neveling K, Kuiper RP, Hoischen A, Nelen MR, Ligtenberg MJ, Tops BB.
Eijkelenboom A, et al. Among authors: hendriks cornelissen sj.
J Mol Diagn. 2016 Nov;18(6):851-863. doi: 10.1016/j.jmoldx.2016.06.010. Epub 2016 Sep 13.
J Mol Diagn. 2016.
PMID: 27637301
Free article.
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Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material.
Steeghs EMP, Kroeze LI, Tops BBJ, van Kempen LC, Ter Elst A, Kastner-van Raaij AWM, Hendriks-Cornelissen SJB, Hermsen MJW, Jansen EAM, Nederlof PM, Schuuring E, Ligtenberg MJL, Eijkelenboom A.
Steeghs EMP, et al. Among authors: hendriks cornelissen sjb.
BMC Cancer. 2020 Apr 7;20(1):291. doi: 10.1186/s12885-020-06785-6.
BMC Cancer. 2020.
PMID: 32264863
Free PMC article.
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Phenotypic and genotypic characterization of orthotopic human glioma models and its relevance for the study of anti-glioma therapy.
Claes A, Schuuring J, Boots-Sprenger S, Hendriks-Cornelissen S, Dekkers M, van der Kogel AJ, Leenders WP, Wesseling P, Jeuken JW.
Claes A, et al.
Brain Pathol. 2008 Jul;18(3):423-33. doi: 10.1111/j.1750-3639.2008.00141.x. Epub 2008 Mar 26.
Brain Pathol. 2008.
PMID: 18371177
Free PMC article.
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